Journal: bioRxiv

Article Title: Single-Cell Resolution of Individual Variation in Hypothalamic Neurons Allows Targeted Manipulation Affecting Social Motivation

doi: 10.1101/2025.03.10.642464

Figure Lengend Snippet: A. Bar plot showing the number of differentially expressed genes (DEGs) per cell type that are upregulated in Achievers (teal; positive values; n = 20) and upregulated in Non-Achievers (gray; negative values, n = 16) (*FDR adjusted p < 0.1, moderated t-test). B. Volcano plot of DEGs in PH-LHA-PVH-SO-PVa Nxph4+ glutamatergic neurons, depicting log2(fold change) versus -log2(adjusted p-value). A-enriched genes (Achiever-enriched) are shown in teal, NA-enriched (Non-Achiever-enriched) in gray, and non-significant (NS) differentially expressed genes in dark gray. Top 10 most signifcant genes are labeled. C. Dot plot showing gene ontology enrichment analysis of achiever-enriched genes (28), with significant biological processes on the y-axis. Dot size represents gene ratio, and color indicates adjusted p-value significance. D. From left to right: summary plot showing the numbers of nuclei and genes detected in each neuronal cluster (clusters shown had significantly different proportions by achiever status before FDR correction OR significant findings in regression analysis); bar plots displaying the proportions across Achiever (teal) and Non-Achiever (gray) animals for each neuronal cluster (One sample (Het_F_5) removed for plotting for STR D1/D2 Gaba cluster); and bar plot showing Beta coefficients with error bars from regression analysis measuring the relationship between cell-type-specific proportions and social rewards. * indicates significant differences at p < 0.05 after FDR corrections. E. Dot plot showing statistical significance (-log10(P-value)) of linear regression analyses for rewards as predicted by neuronal proportions, with hypothalamic regions (indigo) exhibiting marginally more significant differences than other brain regions (gray) (p = 0.08719, Fisher’s). F-G . Linear regression analyses examining relationships between PH-LHA-PVH-SO-PVa Nxph4 + glutamatergic neuron proportions and behavioral outcomes: F. Plot showing a positive relationship between mean rewards and Nxph4 + neuronal proportions, with a stronger effect in males (male: R² = 0.395; female: R² = 0.041). P-values indicate a significant effect of proportions (p = 0.009) and sex (p = 0.005). G. Plot showing no significant relationship between mean distance traveled and Nxph4+ neuronal proportions (male: R² = 0.013; female: R² = 0.023; p=0.505). H. Experimental timeline for chemogenetic inhibition studies (N = 28), showing stereotaxic injection of viral constructs (P49-57) and subsequent testing paradigm with DCZ/saline administration via voluntary oral intake of gelatin cubes during fixed ratio 1 (FR1). I. Schematic showing stereotaxic delivery of AAV5-hSyn-DIO-hM3D(Gi)-mCherry or AAV5-hSyn-DIO-mCherry control virus to the lateral and posterior hypothalamus. J. Representative confocal mosaic reconstruction of immunohistochemistry verification of viral expression in the hypothalamus, with mCherry+ cells in magenta and NeuN+ cells in teal, and DAPI staining all nuclei. K. (Left) Input-output curve showing the number of action potentials elicited after a 600ms driving current during baseline and after 1uM DCZ in mCherry+ cells in the PH (n = 5 cells from 3 animals). p values indicate a significant effect of DCZ on excitability (p = 0.0485; two-way RM ANOVA). (Right) Representative current clamp traces at 50pA (top), 100pA (middle), and 150pA (bottom) during baseline and DCZ in the same cell. L. Rheobase of mCherry+ cells during baseline and after DCZ application (p = 0.0338, paired t-test). M-O. Behavioral outcomes following chemogenetic manipulation indicate inhibition of Nxph4+ neurons in the posterior and lateral hypothalamus significantly reduces mean social rewards (p = 0.006; ANOVA), mean time in investigation zone attempting social interactions (p = 0.006; ANOVA), and overall social motivation, as measured by breakpoint, or the maximum effort exerted for a social interaction (p = 0.016; ANOVA).

Article Snippet: 360 nl of AAV5-hSyn-DIO-hM4D(Gi)-mCherry (diluted to ∼1 x 10 viral particles per mL, Addgene: 44362-AAV5) or AAV5-hSyn-DIO-mCherry (diluted to ∼1 x 10 viral particles per mL, Addgene: 50459-AAV5) was injected into PH/LHA (from bregma: ML +/-0.4 mm, AP -2.3 mm, DV - 4.9 mm).

Techniques: Labeling, Inhibition, Injection, Construct, Saline, Control, Virus, Immunohistochemistry, Expressing, Staining

Journal: Cells

Article Title: Selective Menin Deletion in the Hippocampal CA1 Region Leads to Disruption of Contextual Memory in the MEN1 Conditional Knockout Mouse: Behavioral Restoration and Gain of Function following the Reintroduction of MEN1 Gene.

doi: 10.3390/cells11244019

Figure Lengend Snippet: Figure 2. The transduction of hippocampal neuronal cultures from the MEN1 floxed mice with the virus, pNN.AAV.hSyn.HI.eGFP-Cre.WPRE.SV40. (A) Controls with no virus; (i) GFP signal in the absence of virus; (ii) DAPI for nuclear staining; (iii) merge with GFP and DAPI; (B) CKO with virus transduction by Cre AAV9; (i) GFP signal indicating virus transduction in the preparation with the Cre AAV9; (ii) DAPI for nuclear staining; (iii) merge with GFP and DAPI showing overlap in the neurons expressing GFP and DAPI.

Article Snippet: Ready-to-use AAV9 particles produced from pENN.AAV.hSyn.HI.eGFP-Cre.WPRE.SV40 (#105540) were ordered from Addgene.

Techniques: Transduction, Virus, Staining, Expressing

Journal: Cells

Article Title: Selective Menin Deletion in the Hippocampal CA1 Region Leads to Disruption of Contextual Memory in the MEN1 Conditional Knockout Mouse: Behavioral Restoration and Gain of Function following the Reintroduction of MEN1 Gene.

doi: 10.3390/cells11244019

Figure Lengend Snippet: Figure 3. In vitro virus transduction of the hippocampal neurons from MEN1 floxed mice in control and CKO groups. (A) Controls with no virus; (i) the expression of DAP for nuclear staining; (ii) GFP signal in the absence of virus; (iii) C-menin showing axoplasmic expression; (iv) merge in controls for GFP and DAPI; (B) CKOs with virus; (i) DAPI for nuclear staining; (ii) GFP signal indicating virus transduction in the preparation with the Cre AAV9; (iii) C-menin signal weaker compared to the controls; (iv) merge in the CKO for GFP and DAPI; (C) summary data, showing the reduction in menin signals as measured by mean gray-to-area ratio in the CKO compared to the controls. Data represent the mean ratio ± SEM. n = 4. Statistical significance (Mann–Whitney U test), * p < 0.05.

Article Snippet: Ready-to-use AAV9 particles produced from pENN.AAV.hSyn.HI.eGFP-Cre.WPRE.SV40 (#105540) were ordered from Addgene.

Techniques: In Vitro, Virus, Transduction, Control, Expressing, Staining, MANN-WHITNEY

Journal: Cells

Article Title: Selective Menin Deletion in the Hippocampal CA1 Region Leads to Disruption of Contextual Memory in the MEN1 Conditional Knockout Mouse: Behavioral Restoration and Gain of Function following the Reintroduction of MEN1 Gene.

doi: 10.3390/cells11244019

Figure Lengend Snippet: Figure 4. In vivo virus transduction of the hippocampal CA1 from MEN1 floxed mice in CA1 region of hippocampus and dentate gyrus (DG). (A) Expression of GFP in CA1 in the CKO; (i) the expression of DAPI for nuclear staining in CA1; (ii) the expression of GFP as the marker of virus transduction in the neurons transduced by the AAV9 under the action of synapsin promoter in CA1; (iii) merge in controls with control virus AAV9 GFP and overlap between DAPI and GFP; (B) non-GFP expressing region in dentate gyrus (DG); (i) the expression of DAPI for nuclear staining in DG; (ii) GFP signal in the non-transduced region of hippocampus; (iii) merge for showing the overlap between DAPI and GFP.

Article Snippet: Ready-to-use AAV9 particles produced from pENN.AAV.hSyn.HI.eGFP-Cre.WPRE.SV40 (#105540) were ordered from Addgene.

Techniques: In Vivo, Virus, Transduction, Expressing, Staining, Marker, Control

Journal: Cells

Article Title: Selective Menin Deletion in the Hippocampal CA1 Region Leads to Disruption of Contextual Memory in the MEN1 Conditional Knockout Mouse: Behavioral Restoration and Gain of Function following the Reintroduction of MEN1 Gene.

doi: 10.3390/cells11244019

Figure Lengend Snippet: Figure 6. Ectopic expression in the hippocampus of the mice injected with AAV9 under the function of synapsin promoter and GFP as the marker for the virus transduction. (i) The expression of DAPI for nuclear staining; (ii) GFP as the marker of virus transduction in the neurons transduced by the control AAV9 under the action of synapsin promoter; (iii) merge in controls showing overlap between DAPI and GFP.

Article Snippet: Ready-to-use AAV9 particles produced from pENN.AAV.hSyn.HI.eGFP-Cre.WPRE.SV40 (#105540) were ordered from Addgene.

Techniques: Expressing, Injection, Marker, Virus, Transduction, Staining, Control

Journal: bioRxiv

Article Title: Specific targeting of layer 4 for direct cortical stimulation is not necessary to induce reliable perception

doi: 10.64898/2026.01.08.698338

Figure Lengend Snippet: A Top, Schematics of the intravenous injection. AAV PHP.eB particles were injected in the retro-orbital sinus of Emx1-Cre mice. Bottom, The viral genome contained insert gene coding for ChR2(H134R) fused to eYFP. Black and grey triangles indicate lox2272 and loxP sites. B Fluorescence image of a coronal section from an Emx1-Cre mouse brain showing expression of ChR2(H134R)-eYFP 12 weeks after AAV PHP.eB injection. The neocortex, hippocampus and white matter structures display high fluorescence. The whisker-associated primary somatosensory cortex (wS1) and the internal capsule (IC) are outlined in white boxes (see higher magnification in & ). RS: retro-splenial cortex; DG: dentate gyrus; CA2: subregion of the Cornus Ammonis (CA) in the hippocampus; M1: primary motor cortex; M2: secondary motor cortex; trS1: trunk region of S1. C Left , Section adjacent to the section displayed in panel B and treated with cytochrome C oxidase. Top right , Higher magnification image of wS1. The arrows show three barrels stained in layer 4. Bottom right , Corresponding fluorescence image of wS1 from the section displayed in panel B (white box 1). Arrows indicate low-density spots located in the regions corresponding to the barrels. Thick vertical fiber bundles cross all layers of wS1. D Inset, Fluorescence image of a tangential cortical section of an Emx1-Cre mouse brain 52 weeks after injection, centered on wS1 layer 4. Higher magnification shows low fluorescence in the barrels compared to septa. E Left , Fluorescence image of a coronal section of an Emx1-Cre x Ai32 mouse brain including the wS1 area. Right , Higher magnification shows high fluorescence in the barrels. F Same as D for an Emx1-Cre x Ai32 mouse brain. The higher magnification image shows high fluorescence in the barrels compared to septa. G Schematic of the three main hypotheses explaining the presence/absence of fluorescence in the neuropil of layer 4 in Emx1-Cre mice. The entities expressing or not the transgene could be: (1) thalamo-cortical neurons projections to L4; (2) projections of other neurons from the same column to the L4; (3) neurites of intra-barrel neurons. H,I Left , Transgene fluorescence (green) and NeuN immunostaining (red) from a tangential cortical section including layer 4 of wS1 from an Emx1-Cre mouse injected with PHP.eB mouse brain ( H ) and from an Emx1-Cre x Ai32 mouse ( I ). Middle , neuronal nuclei revealed by NeuN staining show a slightly higher concentration of somas at the barrel walls. Z-projection of 5 scan sections representing a total thickness of 20 µm. An example barrel is outlined in white. Right , Z-projection of transgene eYFP fluorescence from the same sections. wS1 barrels display low fluorescence in Emx1-Cre mouse injected with PHP.eB ( H ) and high fluorescence in Emx1-Cre x Ai32 mouse ( I ). Note that in panel F, the sparse bright eYFP spots do not colocalize with somatic NeuN spots, suggesting they are due to neuropil bundles (see also ). J Schematic representation of the estimated transgene expression level in the membranes of neurites and somata across cortical layers using the PHP.eB viral strategy ( Top ) and the transgenic mouse line strategy ( Bottom ).

Article Snippet: We injected AAV PHP.eB particles (Addgene #127090) to obtain a Cre-dependent expression of ChR2-H134R fused to eYFP in excitatory neurons in all cortical layers (10 Emx1-Cre mice) or in L4 (4 Scnn1a-Cre mice).

Techniques: Injection, Fluorescence, Expressing, Whisker Assay, Staining, Immunostaining, Concentration Assay, Transgenic Assay

Journal: bioRxiv

Article Title: Specific targeting of layer 4 for direct cortical stimulation is not necessary to induce reliable perception

doi: 10.64898/2026.01.08.698338

Figure Lengend Snippet: A Left Fluorescence image of a sagittal section from an Emx1-Cre mouse brain showing expression of ChR2(H134R)-eYFP 4 weeks after AAV PHP.eB injection. The neocortex, hippocampus and white matter structures are regions of high fluorescence. The frontal pole (3) and the hippocampus (4) are outlined in white boxes. As expected with the Emx1 dependency, no fluorescence was observed in the cerebellum (delineated in white). Cerebellar peduncles display a high level of fluorescence as they convey cortico-cerebellar projections. AC: Anterior commissure; CbP: cerebellar peduncles. Middle Higher magnification of inset 3. Cortical layers are delimited, layer 5 displays the highest fluorescence level. L: layer; CC: corpus callosum. Right Higher magnification of inset 4. Among subregions of the Cornus Ammonis (CA), CA2 displays the highest fluorescence level. Fluorescence drops sharply at its boundaries. DG: Dentate gyrus. B Fluorescence image of the transgene superimposed with DAPI staining of a coronal section through the dentate gyrus from an Emx1-Cre mouse brain 4 weeks after AAV PHP.eB injection. Nuclei are densely packed in the granule cell layer and do not co-localize with the transgene. This illustrates that most of the fluorescence from the transgene comes from the neurites and that the opsin is expressed at the neuronal membrane. C Left Fluorescence image of a coronal section through the internal capsule from an Emx1-Cre mouse brain 12 weeks after AAV PHP.eB injection. Higher magnification of inset 2 from . The internal capsule is a pure white matter structure (only axons). Several bundles of fluorescent axons are visible. Right Higher magnification of the inset 5 showing the axon-like morphology of the fluorescent fibers. D Fluorescence image of a coronal section from an Emx1-Cre mouse brain showing expression of ChR2(H134R)-eYFP 12 weeks after AAV PHP.eB injection. As expected, no fluorescence is observed from the midbrain, the hindbrain and the cerebellum due to the Emx1 dependency. Pyramids are fluorescent since they contain cortical axons projecting down to the medulla. IC: Inferior colliculus; Cb: Cerebellum; V4: fourth ventricle; Pyr: Pyramids. E Fluorescence image of a sagittal section from an Emx1-Cre x Ai32 mouse brain. In agreement with , the whole neocortex is fluorescent and the barrels are brighter than the neighboring layers. S1: primary somatosensory cortex; ulS1: upper limb S1; wS1: whisker S1; Vis. & V1: Visual areas and primary visual cortex. F Fluorescence image of a coronal section from a Scnn1a-Cre mouse brain 7 weeks after PHP.eB injection. Layer 4 of the PPC and auditory areas also show the highest fluorescence among their cortical layers. RSP: retro-splenial cortex; PPC: posterior parietal cortex; A1/AUD: primary auditory cortex and auditory areas. G,H Transgene fluorescence (green) and NeuN immunostaining (red) from a tangential cortical section including layer 4 of wS1 from an Emx1-Cre x Ai32 mouse brain ( G ) and from an Emx1-Cre mouse injected with PHP.eB ( H ). These images are higher magnifications of images in . Neuronal nuclei are circled ( Left ) and match with low-fluorescence areas of the eYFP pattern ( Right ), illustrating that the transgene is expressed at the neuronal membrane and not in the cytoplasm.

Article Snippet: We injected AAV PHP.eB particles (Addgene #127090) to obtain a Cre-dependent expression of ChR2-H134R fused to eYFP in excitatory neurons in all cortical layers (10 Emx1-Cre mice) or in L4 (4 Scnn1a-Cre mice).

Techniques: Fluorescence, Expressing, Injection, Staining, Membrane, Whisker Assay, Immunostaining

Journal: bioRxiv

Article Title: Specific targeting of layer 4 for direct cortical stimulation is not necessary to induce reliable perception

doi: 10.64898/2026.01.08.698338

Figure Lengend Snippet: A Top Fluorescence image of a coronal section from two Emx1-Cre mouse brains showing expression of GCamP8m 4 weeks after AAV PHP.eB injection. Apart from the gene of interest (coding for GCamP8m and not ChR2-H134R) the construct is the same as before: Cre dependency and CAG promoter. Part of the whisker S1 area (wS1) is outlined a white box. llS1: lower limb S1; ulS1: upper limb S1; trS1: trunk S1. Bottom Higher magnification of the insets. Fluorescent somas are mostly located in layers 2/3 (L2/3) and layer 5 (L5). Neurons of layer 5 appear brighter than neurons of layer 2/3, probably because of their larger cytoplasm and consequently the higher amount of GCamP8m. There is almost no visible fluorescent soma in layer 4. The background noise and autofluorescence on the right image (mouse n°13) are probably due to the fact that the mouse has not been perfused.

Article Snippet: We injected AAV PHP.eB particles (Addgene #127090) to obtain a Cre-dependent expression of ChR2-H134R fused to eYFP in excitatory neurons in all cortical layers (10 Emx1-Cre mice) or in L4 (4 Scnn1a-Cre mice).

Techniques: Fluorescence, Expressing, Injection, Construct, Whisker Assay

Journal: bioRxiv

Article Title: Specific targeting of layer 4 for direct cortical stimulation is not necessary to induce reliable perception

doi: 10.64898/2026.01.08.698338

Figure Lengend Snippet: A Left Fluorescence image of a coronal section from a Scnn1a-Cre mouse brain 7 weeks after AAV PHP.eB injection, centered on wS1 (white box). Right Higher magnification image of wS1. White arrows indicate layer 4 barrels. B Left Fluorescence image of a tangential section from another Scnn1a-Cre mouse 7 weeks after injection. Right Higher magnification image of wS1. C Same as A from a Scnn1a-Cre x Ai32 mouse brain. Only layer 4 barrels are labelled in wS1. llS1: lower limb S1 area; ulS1: upper limb S1 area; S2: secondary somatosensory area. D Same as C for a tangential section from a Scnn1a-Cre x Ai32 mouse brain, centered on wS1 (white box).

Article Snippet: We injected AAV PHP.eB particles (Addgene #127090) to obtain a Cre-dependent expression of ChR2-H134R fused to eYFP in excitatory neurons in all cortical layers (10 Emx1-Cre mice) or in L4 (4 Scnn1a-Cre mice).

Techniques: Fluorescence, Injection

Journal: bioRxiv

Article Title: Specific targeting of layer 4 for direct cortical stimulation is not necessary to induce reliable perception

doi: 10.64898/2026.01.08.698338

Figure Lengend Snippet: A Left , Schematics of the setup. An Emx1-Cre mouse injected with AAV PhP.eB particles was head-fixed under anaesthesia. A 32-channel silicon probe was inserted below the cranial window through a small opening. We recorded neuronal activity while projecting light spots with a digital projector (DLP) through the intact part of the window. Fifteen different spots were projected in pseudo-random sequences, according to a 3×5 stimulation matrix centered above the inserted probe. Right , image of the cranial window with the electrode penetrating the cortex from the side. A sketch of the light spots and of the electrode shank are overlaid. B Mean firing rates of all 5 single units before and during the photostimulation protocol (not specifically after a given spot projection). All units showed an increased activity (Wilcoxon test, * p < 0.05). C Raster plots of action potentials for one single unit, centered on the beginning of the first flash of spot 1 (Top) and spot 11 (Bottom). Four to five phase-locked peaks of response were observed in response to spot 11 while spot 1 didn’t trigger any activity. D Average increase in the number of action potentials per second during the 80 ms following a light spot onset compared to the baseline period activity, for each of the 15 light spots. Same neuron as panel C. E Detection task. Scnn1a-Cre mice injected with AAV.PHP.eB (carrying the gene coding for ChR2-H134R) or control mice were head-fixated under the same DLP system as in A. Mice were awake and water-restricted. For each trial, an optogenetic spot (300 µm diameter) was projected onto the window, either targeting the C2 barrel or targeting the dental cement (sham catch trial). The mouse had to lick a spout to obtain a water reward in the two seconds following the stimulus start. A masking blue light was directed towards the eyes to mask the projection of spots. F Timeline of a single trial. Each trial started with a No Lick Period of random duration (between 3 and 5 s). This period was reset by each lick to force the mice to stop licking and focus on detecting the stimulation. Then, the stimulus was projected during 500 ms: 50 flashes of 5 ms separated by 5 ms (same duty cycle as in ). The trials in which the spot was projected onto the cement accounted for 10% of the total, with one catch trial randomly placed per group of 10 trials. From the first flash, the mouse had 2 seconds to lick the spout twice in order to receive a reward (Reaction period). Licks to both cortical and cement spots were rewarded by a water droplet. Finally, an intertrial period (6 to 8 s long) allowed the mouse to drink its reward before the start of the next trial. G Licking activity for the Scnn1a-Cre mouse injected with the virus (“only L4”) during session 9 of the detection task. Top , Raster plots of licks during all trials of the session. The type of trial (spot onto cortex or cement) is shown by a colored tick on the left (cortex black, cement red) and by the matching color of the licks. Bottom , Mean lick distribution computed over all trials of the session, for trials in which the light spot was projected onto the cortex (black) or cement (red). Time 0 corresponds to the beginning of the first optogenetic flash.

Article Snippet: We injected AAV PHP.eB particles (Addgene #127090) to obtain a Cre-dependent expression of ChR2-H134R fused to eYFP in excitatory neurons in all cortical layers (10 Emx1-Cre mice) or in L4 (4 Scnn1a-Cre mice).

Techniques: Injection, Activity Assay, Control, Virus

Journal: bioRxiv

Article Title: Specific targeting of layer 4 for direct cortical stimulation is not necessary to induce reliable perception

doi: 10.64898/2026.01.08.698338

Figure Lengend Snippet: A Top, Detection task, same as . Bottom , Rationale of the task design. We wanted to figure out if the detection of the optogenetic flash was due to the activity it induced or by sensing it in any other way. By rewarding both spots, the mouse had every reason to lick as soon as it detected a spot, whether optogenetically or visually. Thus, the absence of licking for the spot on the cement indicates that it was not detected. B Licking activity for the Scnn1a-Cre mouse injected with the virus (“only L4”) during session 9 of the detection task. Top, Middle Same as . Bottom, For each trial, we quantified the delay for ‘lick onset’ as the time of the first lick after the start of stimulation (reaction time). The mean lick onset distribution was computed over all trials of the session, same color convention as in . The distribution of lick onset delays showed a single narrow peak (mean +/- s.d. = 689 +/- 189 ms). As the duration of the No Lick Period was random, this fixed reaction time to the stimulation further indicated that the mouse was indeed guided by the cue and not exploiting a timing strategy. C Left, Same representations as in B for a Scnn1a-Cre control mouse (no virus injected) during session 9 of the detection task. Left Top , Raster plots of licks. Left Middle, The lick distributions for both spots, through the window and on the cement, were similar, suggesting that there was no activation of neurons or retinal photoreceptors by light from the projector entering through the cranial window. Left Bottom, The distribution of lick onsets was not concentrated around one reaction time but as very broad (mean +/- s.d. = 540 +/- 455 ms), suggesting random initiation of licking bursts after the necessary still No-lick period. See also panel D. Right, Same analysis as Left for session 10 in the same control mouse, during which a spot was presented on wS1 or no stimulation was presented (no light or any cue at all) (purple curve and ticks). Top and Middle, In the absence of any stimulation, the animal still licked in the same way as it did for the spot on the cortex. Bottom, Reaction times to both spots were also similar. Overall, this suggests that the apparent detection of both spots by the control mouse was merely the effect of recurrent and sustained licking, i.e., a timing strategy that the mouse developed to take advantage of the temporal structure of the task. Due to technical issues, two consecutive partial sessions were run and pooled for each of sessions 9 ( Left ) and 10 ( Right ) of the control mouse. D Distributions of trial durations during session 9 for the virus-injected (green) and the control mice (orange). The duration of a trial was computed as the time spent in the No Lick Period (including all the resets) and the reaction period. The best theoretical mean trial duration (without any reset of the No Lick Period) would be 6 s. Arrows indicate the mean trial duration. Trial durations were much longer for the control mouse (up to 98 s, mean +/- s.d. = 25.6 +/-20.0 s) compared to the PhP.eB injected mouse (mean +/- s.d. = 6.6 +/- 1.7 s), mostly because of repeated resetting of the No Lick period. This difference confirmed the use of a timing strategy in the absence of opsin expression.

Article Snippet: We injected AAV PHP.eB particles (Addgene #127090) to obtain a Cre-dependent expression of ChR2-H134R fused to eYFP in excitatory neurons in all cortical layers (10 Emx1-Cre mice) or in L4 (4 Scnn1a-Cre mice).

Techniques: Activity Assay, Injection, Virus, Control, Activation Assay, Expressing

Journal: bioRxiv

Article Title: Specific targeting of layer 4 for direct cortical stimulation is not necessary to induce reliable perception

doi: 10.64898/2026.01.08.698338

Figure Lengend Snippet: A Left, Sensory-guided licking task. A rotating light bar was projected on wS1 through a cranial window by a digital light processor (DLP). A water tube detected licks and delivered rewards when adequate. Right, An example image of the cortical surface during optogenetic stimulation (the white bar corresponds to blue light in grey scale). B Position of the stimulation space (blue circle) on the cortical functional map (grey) in S1. The space is centered on the C2 barrel and is restricted to the wS1 area. The map contours were adapted from , and , and positioned according to intrinsic imaging of several barrels (panel C). C Example mapping of wS1 barrels under anesthesia prior to training. Left, Contours of intrinsic imaging responses to single whisker stimulations (Alpha, Gamma, C2 and Delta whiskers) superimposed on an image of the cortical surface. Right , Temporal light fluctuations (ΔI/I0) of the corresponding regions of interest during trials. The stimulation period is indicated by the grey shading. D Left, Different zones of the stimulation space. When the bar was in the Rewardable zone (green), licks were rewarded. In the No-lick zone (red), a lick ended the trial. In the Neutral zones (white), licks were ignored. Right, Snapshots of an example trial showing the displacement of the light bar on the barrel cortex. E Spatial distribution of the optogenetic bar angle at all lick timestamps for one example Emx1-Cre mouse trained 5 weeks after AAV PHP.eB injection, for the 1st and the 10th (Last) sessions. F Average proportions (mean ± s.e.m) of all licks for which the optogenetic bar was in the Rewardable (green), No-lick (red), and Neutral zones (black) during training of Emx1-Cre mice injected with PHP.eB of the “all layers except L4” group (n = 5). The “Last” session consists of the 10th session for two mice and the 15th for three mice. Wilcoxon test, * p < 0.05. G Average proportions (mean ± s.e.m) of all licks during training (same quantification as F ). Left, Mean values from the first and last sessions for Emx1-Cre mice injected with PHP.eB (n = 5). Middle, Same for two Scnn1a-Cre mice (A and B) injected with PHP.eB (n = 2). Right, Same for Emx1-Cre x ChR2-tdT mice (n = 8). The “Last” session differs between groups, see panel H. Wilcoxon test * p < 0.05. H Left, Schematics of expression profile for the three groups: ‘all layers except L4’ Emx1-Cre + virus (purple), ‘only L4’ Scnn1a-Cre + virus (pink) and ‘all layers’ Emx1-Cre x Ai27 (green) mice. Blue light intensity was adapted to the cortical depth of opsin-expressing cells (see Methods). Right, Individual learning curves, quantified by the percentage of rewarded trials normalized by subtracting the chance level (see Methods). Same color code. I Learning speed measurement. Number of training sessions (one per day) to reach at least 10% of rewarded trials after normalization (corresponding to around 30% of raw percentage, ). Each circle represents a mouse. Same color code as panel H . The empty circle (n.a) represents an animal that never exceeded the chance level.

Article Snippet: We injected AAV PHP.eB particles (Addgene #127090) to obtain a Cre-dependent expression of ChR2-H134R fused to eYFP in excitatory neurons in all cortical layers (10 Emx1-Cre mice) or in L4 (4 Scnn1a-Cre mice).

Techniques: Functional Assay, Imaging, Whisker Assay, Injection, Expressing, Virus

Journal: bioRxiv

Article Title: Specific targeting of layer 4 for direct cortical stimulation is not necessary to induce reliable perception

doi: 10.64898/2026.01.08.698338

Figure Lengend Snippet: A Raw (Left) and normalized (Right) learning curves quantified by the percentage of rewarded trials for Emx1-Cre mice injected with PHP.eB (n = 5, A ); Scnn1a-Cre mice injected with PHP.eB (n = 2, B ); and Emx1-Cre x ChR2-tdT mice (n = 8, C ). The normalized rewarded trial percentage is obtained by subtracting the chance level (see Methods). For the three mouse groups, the raw learning curves have similar shapes and dynamics to the corresponding normalized ones. The “Last” session differs between groups. For the group Emx1-Cre + virus, 2 mice were trained up to day 10 and three up to day 15. Scnn1a-Cre + virus mice were trained up to day 15 and 19. For the Emx1-Cre x Ai27 group, five mice were trained up to day 5, two mice up to day 7 and one up to day 10. Curves on the right are the same as but truncated. Wilcoxon tests, * p < 0.05., ** p < 0.01.

Article Snippet: We injected AAV PHP.eB particles (Addgene #127090) to obtain a Cre-dependent expression of ChR2-H134R fused to eYFP in excitatory neurons in all cortical layers (10 Emx1-Cre mice) or in L4 (4 Scnn1a-Cre mice).

Techniques: Injection, Virus

Journal: Molecular Therapy. Methods & Clinical Development

Article Title: Engineering a highly durable adeno-associated virus receptor for analytical applications

doi: 10.1016/j.omtm.2023.101157

Figure Lengend Snippet: Analysis of various AAV serotypes using the AVR-NPR column (A) Chromatograms when purified AAVs were subjected to the AVR-NPR column. The AAV serotypes and injection amounts are indicated on each chromatogram’s right side. The black lines indicate the relative fluorescence intensity, and the gray polygonal line represents the ratio of mobile phase A (15 mM sodium acetate, 10 mM glycine, and 50 mM CaCl 2 [pH 4.5]) and B (15 mM sodium acetate, 10 mM glycine, and 50 mM CaCl 2 [pH 2.2]), where the ratio of B increases linearly from 0% to 100% between 5 and 65 min after the start of the measurement. (B) Chromatograms when (a–f) a mixture of AAV1 and AAV2 in different ratios and (g) chimeric AAV1/2 were subjected to the AVR-NPR column. The black lines indicate the relative fluorescence intensity. The vertical red and blue dashed lines represent the top elution peak positions of AAV1 and AAV2, respectively. (C) Particle sizes of AAV1, AAV2, and AAV1/2 in DLS. (D) Plots of the retention time against the transduction efficiency of each AAV2 mutant from Table 1 when analyzed using the AVR-NPR column. The black dotted line represents exponential trendline calculated from each plot. The R-squared value of the trendline is shown in the graph.

Article Snippet: To assess the AAV particle size and shape, the DLS of purified AAV was measured using the Zetasizer Ultra (Malvern Panalytical).

Techniques: Purification, Injection, Fluorescence, Transduction, Mutagenesis

Journal: Molecular Therapy. Methods & Clinical Development

Article Title: Engineering a highly durable adeno-associated virus receptor for analytical applications

doi: 10.1016/j.omtm.2023.101157

Figure Lengend Snippet: Analysis of Crude AAV samples using the AVR-NPR column (A) Chromatograms of the purified AAV8 (black), AAV8-mixed cell-cultured supernatant (purple), and AAV8-mixed cell-lysed supernatant (red). The gray polygonal line represents the ratio of mobile phase A (15 mM sodium acetate, 10 mM glycine, and 50 mM CaCl 2 [pH 4.5]) and B (15 mM sodium acetate, 10 mM glycine, and 50 mM CaCl 2 [pH 2.2]), where here the ratio of B increases linearly from 0% to 100% between 30 and 75 min after the start of the measurement. (B) Quantification of AAV8 using the AVR-NPR column and ELISA. The bars show the purified AAV8 (gray), AAV8-mixed cell-cultured supernatant (purple), and AAV8-mixed cell-lysed supernatant (red). The capsid titers quantified with each purified AAV8 are shown as 1 and the other capsid titers as relative values. The analyses were performed in triplicate, and the error bars indicate the standard deviation. (C–F) Expression monitoring of AAV8. Chromatograms of (C) cell-cultured and (D) cell-lysed supernatants expressing AAV8 at days 1, 2, 3, 4, and 7 after the transfection. The gray polygonal line represents the ratio of mobile phase A and B, where here the ratio of B increases linearly from 0% to 100% between 30 and 75 min after the start of the measurement. (E) Quantification of the AAV8 capsid titers for each sample in (C) and (D). The results of cell-cultured supernatants quantified by the AVR-NPR column and ELISA are plotted as gray squares with solid and dotted lines, respectively. In contrast, the results of cell-lysed supernatants quantified by the AVR-NPR column and ELISA are plotted as black circles with solid and dotted lines, respectively. (F) Correlation functions between the AAV8 capsid titers quantified by the AVR-NPR column and ELISA. Gray squares and black circles were plotted based on the quantification results of cell-cultured and cell-lysed supernatant in (E), respectively. Each dotted line indicates the linear trendline calculated from the plots. R-squared values of the trendlines are shown in the graph.

Article Snippet: To assess the AAV particle size and shape, the DLS of purified AAV was measured using the Zetasizer Ultra (Malvern Panalytical).

Techniques: Purification, Cell Culture, Enzyme-linked Immunosorbent Assay, Standard Deviation, Expressing, Transfection

Journal: Advanced Science

Article Title: Extracellular LCN2 Binding to 24p3R in Astrocytes Impedes α‐Synuclein Endocytosis in Parkinson's Disease

doi: 10.1002/advs.202501694

Figure Lengend Snippet: Astrocytic LCN2 overexpression aggravates PD‐like pathology and α‐Syn accumulation in mice. A) Diagram of the experimental design. IHC results confirm that AAV‐Lcn2 (mCherry) is expressed, mainly in GFAP + astrocytes (green). B) The time taken to descend a pole (Time‐total) was recorded in pole test in MPTP model (n = 14 animals for each group). C) Time on the rod was measured by the rotarod test in MPTP model (n = 12 animals for each group). D) Movement distance within 5 min was recorded in open field test in MPTP model (n = 9 animals for each group). E,F) Microphotographs and stereological counts of TH‐positive neurons in the SNpc in MPTP model (n = 6 animals for each group). G,H) Representative immunoblots and quantification of relative expression of TH in the SNpc in MPTP model (n = 6 animals for each group). I) Immunohistochemical staining and quantification of Nissl‐positive cells in the SNpc in MPTP model. J) Microphotographs and quantification of GFAP‐positive astrocytes and Iba1‐positive microglia in the SNpc in MPTP model (n = 6 animals for each group). K) Movement distance within 5 min was recorded in AAV‐control or AAV‐LCN2‐injected mice in α‐Syn PFF model (n = 16 animals for each group). L) The time taken to descend a pole (Time‐total) was recorded in pole test in α‐Syn PFF model (n = 16 animals for each group). M) Time on the rod was measured by the rotarod test in α‐Syn PFF model (n = 16 animals for each group). N) Immunohistochemical staining and quantification of TH‐positive cells in the SNpc in α‐Syn PFF model (n = 5 animals for each group). O) Immunohistochemical staining and quantification of Nissl‐positive cells in the SNpc in α‐Syn PFF model (n = 5 animals for each group). P–R) Representative immunoblots (P) and quantification of relative expression of TH (Q) and LCN2 (R) in the SNpc in α‐Syn PFF model (n = 5 animals for each group). S–U) Representative immunoblots and quantification of relative expression of TX‐insoluble and TX‐soluble α‐Syn and p‐α‐Syn in the SNpc in α‐Syn PFF model (n = 4‐5 animals for each group). V) Representative double immunostaining for p‐Syn (red) and TH (green) in the SNpc in α‐Syn PFF model (n = 5 animals for each group). The data shown are the mean ± SEM. Two‐way ANOVA with Tukey's post‐hoc test was used (B–D, F, H–J) and Unpaired t test was used (K‐O, Q‐R, T‐V). * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: AAV particles (AAV‐m‐Lcn2‐GFAP promoter‐MCS 3FLAG hGH PolyA, GOSV0334717) were purchased from Shanghai GeneChem Co. (Shanghai, China). pAAV‐GFaABC1D‐EGFP‐3×FLAG‐miR30‐shRNA (mSlc22a17)‐WPRE were purchased from OBiO Technology (Shanghai, China). rAAV‐GFaABC1D‐EGFP‐5′miR‐30a‐shRNA (mLcn2)‐3′‐miR30a‐WPREs and rAAV‐CMV‐SYN‐SNCA (WT)‐WPRE‐bGHpA were purchased from BrainVTA Technology (Wuhan, China).

Techniques: Over Expression, Western Blot, Expressing, Immunohistochemical staining, Staining, Control, Injection, Double Immunostaining

Journal: Advanced Science

Article Title: Extracellular LCN2 Binding to 24p3R in Astrocytes Impedes α‐Synuclein Endocytosis in Parkinson's Disease

doi: 10.1002/advs.202501694

Figure Lengend Snippet: Astrocytic LCN2 ablation alleviates α‐Syn pathology. A) Diagram of the experimental design. IHC results confirm that AAV‐LCN2 shRNA (EGFP) is expressed, mainly in GFAP + astrocytes (red) in α‐Syn PFF model. B,C) Movement distance within 5 min was recorded in open field test (n = 11‐13 animals for each group). D) Time on the rod was measured by the rotarod test (n = 11‐12 animals for each group). E‐F) the time taken to turn around (Time‐turn) and descend a pole (Time‐total) was recorded in pole test (n = 10‐12 animals for each group). G‐H) Microphotographs and stereological counts of TH‐positive neurons in the SNpc (n = 6‐7 animals for each group). I,J) Representative immunoblots and quantification of relative expression of TH in the SNpc (n = 6 animals for each group). K,L) Immunohistochemical staining and quantification of Nissl‐positive cells in the SNpc. M) Microphotographs of GFAP‐positive astrocytes and Iba1‐positive microglia in the SNpc. N,O) Stereological counts of GFAP‐positive astrocytes (N) and Iba1‐positive microglia (O) in the SNpc (n = 6 animals for each group). P) Representative double immunostaining for p‐Syn (red) and TH (green) in the SNpc. Q) Quantification of p‐Syn fluorescence intensity in P (n = 4‐5 animals for each group). DAPI stains nucleus (blue). R–T) Representative immunoblots and quantification of relative expression of TX‐insoluble and TX‐soluble α‐Syn and p‐α‐Syn in the SNpc (n = 5‐6 animals for each group). The data shown are the mean ± SEM. Two‐way ANOVA with Tukey's post‐hoc test was used (C‐F, H, J, L, N‐O) and Unpaired t test was used (Q‐S). * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: AAV particles (AAV‐m‐Lcn2‐GFAP promoter‐MCS 3FLAG hGH PolyA, GOSV0334717) were purchased from Shanghai GeneChem Co. (Shanghai, China). pAAV‐GFaABC1D‐EGFP‐3×FLAG‐miR30‐shRNA (mSlc22a17)‐WPRE were purchased from OBiO Technology (Shanghai, China). rAAV‐GFaABC1D‐EGFP‐5′miR‐30a‐shRNA (mLcn2)‐3′‐miR30a‐WPREs and rAAV‐CMV‐SYN‐SNCA (WT)‐WPRE‐bGHpA were purchased from BrainVTA Technology (Wuhan, China).

Techniques: shRNA, Western Blot, Expressing, Immunohistochemical staining, Staining, Double Immunostaining, Fluorescence

Journal: Advanced Science

Article Title: Extracellular LCN2 Binding to 24p3R in Astrocytes Impedes α‐Synuclein Endocytosis in Parkinson's Disease

doi: 10.1002/advs.202501694

Figure Lengend Snippet: Astrocytic 24p3R deletion promotes α‐Syn spread and toxicity in α‐Syn PFF model. A) Schematic representation of the chambers in which neurons were co‐cultured with vector or 24p3R‐overexpressed astrocytes. α‐Syn PFF (1 µg mL −1 ) was added to chambers for 10 days. B) Representative double‐immunostaining for p‐α‐Syn (green) and MAP2 (red) when neurons were co‐cultured with vector or 24p3R‐overexpressed astrocytes after α‐Syn PFF (1 µg mL −1 ) treatment for10 days. C,D) Quantification of p‐α‐Syn in neuron and mean total neurites length in B (Six independent experiments). E) Diagram of the experimental design. IHC results confirm that AAV‐24p3R shRNA (EGFP) is expressed, mainly in GFAP + astrocytes (red) in α‐Syn PFF model. F) Representative double immunostaining for p‐Syn (red) and TH (green) in the SNpc. G) Quantification of p‐Syn fluorescence intensity in F (n = 6 animals for each group). DAPI stains nucleus (blue). H–J) Representative immunoblots and quantification of relative expression of TX‐insoluble and TX‐soluble α‐Syn and p‐α‐Syn in the SNpc (n = 5‐6 animals for each group). K) Representative images showing α‐Syn signals in the hippocampus, prefrontal cortex and striatum region from AAV‐control and AAV‐24p3R shRNA mice. L,M) Microphotographs and stereological counts of TH‐positive neurons in the SNpc (n = 6 animals for each group). N,O) Immunohistochemical staining and quantification of Nissl‐positive cells in the SNpc (n = 5 animals for each group). P‐R) Representative immunoblots (P) and quantification of relative expression of TH (Q) and LCN2 (R) in the SNpc (n = 3 animals for each group). S) Movement distance within 5 min was recorded in open field test (n = 8 animals for each group). T) Time on the rod was measured by the rotarod test (n = 8‐10 animals for each group). U) The time taken to descend a pole (Time‐total) was recorded in pole test (n = 8 animals for each group). V,W) The percentage of time spent in the novel arm and the number of entries into novel arm were recorded in Y maze test (n = 8‐10 animals for each group). X) Proposed model for how LCN2 impedes the α‐Syn uptake by astrocytes in PD. The data shown are the mean ± SEM. Unpaired t test was used (C, G‐I) and two‐way ANOVA with Tukey's post‐hoc test was used (D, M, O, Q‐W). * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: AAV particles (AAV‐m‐Lcn2‐GFAP promoter‐MCS 3FLAG hGH PolyA, GOSV0334717) were purchased from Shanghai GeneChem Co. (Shanghai, China). pAAV‐GFaABC1D‐EGFP‐3×FLAG‐miR30‐shRNA (mSlc22a17)‐WPRE were purchased from OBiO Technology (Shanghai, China). rAAV‐GFaABC1D‐EGFP‐5′miR‐30a‐shRNA (mLcn2)‐3′‐miR30a‐WPREs and rAAV‐CMV‐SYN‐SNCA (WT)‐WPRE‐bGHpA were purchased from BrainVTA Technology (Wuhan, China).

Techniques: Cell Culture, Plasmid Preparation, Double Immunostaining, shRNA, Fluorescence, Western Blot, Expressing, Control, Immunohistochemical staining, Staining