Journal: Bioactive Materials

Article Title: Splenic dendritic cell-targeting mRNA transfection of H-type ionizable lipid-based LNPs for enhancing tumor immunotherapy

doi: 10.1016/j.bioactmat.2026.02.018

Figure Lengend Snippet: In vivo DC maturation and T cell activation in C57BL/6J mice induced by mOVA/H 18 NPs through intravenous injection. C57BL/6J mice were vaccinated with different formulations on Day 0 and Day 5. On Day 10, the spleens of mice were collected and analyzed by flow cytometry. Quantification analysis of (A) CD80 + CD86 + DCs and (B) CD40 + DCs in the spleen. Quantification analysis of (C) CD3 + CD4 + T cells and (D) CD3 + CD8 + T cells in the spleen. (E) Quantification analysis and (F) representative flow cytometry contour plots of OVA-specific CD8 + T cells among all cell populations in the spleen. (G) Quantification analysis and (H) representative flow cytometry contour plots of IFN-γ + CD8 + T cells among all cell populations in the spleen. (I) Quantification results and (J) representative images of IFN- γ -secreting immune cells in the spleen of mice analyzed by enzyme-linked immunospot (ELISpot) assay. Data were shown as mean ± SD (n = 3).

Article Snippet: Quantification analysis of (C) CD3 + CD4 + T cells and (D) CD3 + CD8 + T cells in the spleen. (E) Quantification analysis and (F) representative flow cytometry contour plots of OVA-specific CD8 + T cells among all cell populations in the spleen. (G) Quantification analysis and (H) representative flow cytometry contour plots of IFN-γ + CD8 + T cells among all cell populations in the spleen. (I) Quantification results and (J) representative images of IFN- γ -secreting immune cells in the spleen of mice analyzed by enzyme-linked immunospot (ELISpot) assay.

Techniques: In Vivo, Activation Assay, Injection, Flow Cytometry, Enzyme-linked Immunospot

Journal: Journal of Cell Science

Article Title: OptoLoop – an optogenetic tool to probe the functional role of genome organization

doi: 10.1242/jcs.264574

Figure Lengend Snippet: Optogenetic manipulation of proximity between repetitive genomic loci. (A) Scheme of OptoLoop consisting of a fusion between dCas9 and the optogenetic protein CRY2. OptoLoop is targeted to specific genomic loci by introducing specific sgRNAs. CRY2–CRY2 interactions activated by blue light bridge targeted loci to form a chromatin loop. (B) Left panel, region of chromosome 19 showing sgIDR3 and sgTCF3 target sites, representative Hi-C contact map (data from ) and BACs used in DNA-FISH to label the IDR3 (magenta) and TCF3 loci (green). Right panel, mCherry channel images of U2OS dCas9–3XmCherry–CRY2 cells transfected with sgIDR3 and sgTCF3, kept in dark or illuminated with blue light for 3 h (1 s pulses every 10 s), and fixed. Scale bars: 5 µm. (C) Left panel, representative image of DNA-FISH for IDR3 and TCF3 with specific BAC FISH probes in U2OS cells. Right panel represents a single cell highlighted in left panel (yellow box); the expansion shows a single allele in this cell. Dashed line denotes the distance between the two FISH signals. Scale bars: 20 µm (left panel), 5 µm (right panel), 1 µm (expansion). (D) IDR3–TCF3 distances, calculated for U2OS dCas9–mCherry–CRY2 polyclonal cells transfected with indicated combinations of sgIDR3 and sgTCF3, kept under dark or illuminated for 3 h (1 s pulses every 10 s). Violin plot corresponds to a representative experiment, with black lines representing median distances. Bar plot represents means of two independent experiments. Each dot represents the median of typically 5000–10,000 alleles analyzed per experiment. (E) Fraction of alleles with IDR3-TCF3 distance <0.27 µm measured from DNA-FISH images for U2OS dCas9–mCherry–CRY2 polyclonal cells and three clones of U2OS dCas9–3XmCherry–CRY2 cells, transfected with indicated combinations of sgIDR3 and sgTCF3, and kept in dark or illuminated for 3 h (1 s pulses every 10 s). Each dot represents the fraction of typically 5000–10,000 alleles analyzed per experiment. Bars represent means of two or three independent experiments. (F) Measurement of cell-to-cell heterogeneity in loop formation. Bars with green shades: observed fraction of cells with none, one or both alleles with IDR3–TCF3 distance <0.27 µm obtained from a representative experiment shown in E with 2500–5000 cells analyzed per sample. Bars with magenta shades: expected fraction of cells with none, one or both alleles with IDR3–TCF3 distance <0.27 µm assuming that alleles from a same cell are independent between each other (Eqn 2). * P <0.05; *** P <0.001; ns, not significant [two-way ANOVAs followed by post-hoc Tukey tests (D,E); paired two-tailed t -test (E); chi-squared test (F)].

Article Snippet: Synthetic single-guide RNAs (sgRNAs) were custom-ordered from Synthego (Reedwood City, CA, USA) and are listed in . sgRNAs were synthesized with a 2′-O-methyl modification at the three first and last bases, and 3′ phosphorothioate bonds between the third- and second-last bases for increased stability.

Techniques: Hi-C, Transfection, Single Cell, Clone Assay, Two Tailed Test

Journal: Journal of Cell Science

Article Title: OptoLoop – an optogenetic tool to probe the functional role of genome organization

doi: 10.1242/jcs.264574

Figure Lengend Snippet: Functional effects of genome organization manipulation on gene regulation. (A) Scheme of ‘telomere position effect over long distances’ model. Gene repression by long-range looping with telomere depends on telomere length. (B) Region of chromosome 5 showing sgSubtel (sgSubtel1+sgSubtel2) and sgTERT (sgTERT1+sgTERT2) target sites, and BACs used in DNA-FISH to label the 5p subtelomeric region (Subtel, green) and the TERT locus (magenta). (C) Left panel, representative image of DNA-FISH with Subtel and TERT BAC probes in HeLa cells. Scale bar: 5 µm. Right panel, fraction of alleles with Subtel- TERT distance <0.27 µm measured from DNA-FISH images of HeLa cells stably expressing dCas9-3XGFP-CRY2, transfected with none or sgSubtel and sgTERT sgRNAs, and kept under dark or illuminated with blue light for 3 h (1 s pulses every 10 s). Each dot represents the fraction of typically 6000–20,000 alleles analyzed per experiment. Bars represent the means of two experiments. Values are represented as relative to control (no sgRNAs, no light). (D) Representative image of RNA/DNA-FISH with RNA probes against TERT pre-mRNA and Subtel and TERT BAC probes in HeLa. Expansion shows a single allele (highlighted with a yellow square). Scale bars: 5 µm (left image), 1 µm (expansion). (E) Number of active TERT transcription sites (TSs) per cell (left panel) and total TERT pre-mRNA intensity (right panel) measured from RNA/DNA-FISH images from HeLa cells stably expressing dCas9–3XGFP–CRY2, transfected with none or sgSubtel and sgTERT sgRNAs, and illuminated with blue light for 4 h (1 s pulses every 10 s). Cells were binned according to their fraction of alleles with Subtel- TERT distance <0.27 µm. Average measurements from the whole population of cells (i.e. not binned) are also shown. Each dot represents the mean of typically 150–1500 cells analyzed per bin, per experiment. Bars represent the means of two experiments. RNA total intensity was normalized to that of control (bin ‘0’, no sgRNAs). (F) Fraction of alleles with Subtel- TERT distance <0.27 µm for alleles classified as active or inactive regarding TERT transcription. Allele transcription status was determined according to the presence or absence of an RNA-FISH signal at a distance <2.5 µm. Data obtained from RNA/DNA-FISH images of HeLa cells stably expressing dCas9–3XGFP–CRY2, transfected with none or sgSubtel and sgTERT sgRNAs, and illuminated with blue light for 4 h (1 s pulses every 10 s). Each dot represents the mean of typically 400–2000 alleles analyzed per condition, per experiment. Bars represent the means of two independent experiments. (G) Fraction of alleles with Subtel– TERT distance <0.27 µm (left panel) and average number of active TERT transcription sites per cell (right panel) measured from a representative RNA/DNA-FISH experiment shown in (E). Cells were binned according to their mean GFP nuclear intensity. Average measurements from whole population of cells (i.e. not binned) are also shown. Each dot represents the fraction of 300–1800 alleles analyzed per bin (left panel) or the mean of 100–600 cells analyzed per bin (right panel). * P <0.05; ** P <0.01; *** P <0.001 [two-way ANOVAs followed by post-hoc Tukey tests (C,E,F and G, right panel); Marascuilo's procedure (G, left panel)].

Article Snippet: Synthetic single-guide RNAs (sgRNAs) were custom-ordered from Synthego (Reedwood City, CA, USA) and are listed in . sgRNAs were synthesized with a 2′-O-methyl modification at the three first and last bases, and 3′ phosphorothioate bonds between the third- and second-last bases for increased stability.

Techniques: Functional Assay, Stable Transfection, Expressing, Transfection, Control