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Image Search Results
Journal: The Journal of cell biology
Article Title: Mechanosensitive calcium flashes promote sustained RhoA activation during tight junction remodeling.
doi: 10.1083/jcb.202105107
Figure Lengend Snippet: Figure 5. Junction elongation induces Rho flares. (A) Graph showing that calcium flash (GCaMP6m) follows junction elongation (verted-to-vertex length) and precedes Rho-mediated junction contraction and stabilization of length. Time 0 s represents start of Rho flare. Shaded region represents SEM; n = 16 flares, 13 embryos, 10 experiments. (B) Schematic of mosaic injection and regional activation of Rho-mediated contractility using optogenetics. Top: Schematic showing the mosaic injection of optogenetic constructs (prGEF and LOVpep) injected into one cell, while active Rho probe is injected in both cells at two-cell stage. Bottom: Regional activation of RhoA using optogenetics in region of stimulation (shaded gray box) and quantification of junction length and frequency of Rho flares in region of observation (dotted blue box). (C) Cell view of an embryo mosaically-expressing prGEF (2xPDZ-YFP-LARG(DH), yellow) and active Rho probe (mCherry-2xrGBD, gray). (C9) Cell view of Rho probe in the embryo from C. Regional stimulation (white dashed box) induces Rho flares in areas neighboring the region of stimulation (yellow arrowheads). (D) Quantification of Rho flares in the area outside the region of stimulation shown in C9. Frequency of Rho flares occurring pre-stimulation (0–300 s) and post-stimulation (600–900 s) are matched for color and shape. Significance calculated using unpaired two-tailed t test; n = 6 embryos, 4 experiments. (E) Time-lapse montage of a junction highlighted in C9 (yellow box) expressing active Rho probe (mCherry- 2xrGBD). Following optogenetic stimulation (indicated by gray shaded box), an increase in junction length precedes Rho flare activation (yellow arrowhead). Junction length measured from vertex to vertex is indicated under each panel.
Article Snippet: Stargazin-GFP-LOVpep (referred to as GFPLOVpep) was generated by PCR amplifying the
Techniques: Injection, Activation Assay, Optogenetics, Construct, Expressing, Two Tailed Test
Journal: Neuron
Article Title: Endocannabinoid Signaling Collapse Mediates Stress-Induced Amygdalo-Cortical Strengthening
doi: 10.1016/j.neuron.2019.12.024
Figure Lengend Snippet: Key Resource Table
Article Snippet: Also see . table ft1 table-wrap mode="anchored" t5 caption a7 REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies Rabbit-α-cFOS Abcam 190289 RRID: AB_443538 Alexafluor 488 Donkey-α-Rabbit Invitrogen A21206 RRID: AB_221544 Rabbit-α-DAGLα Gift from Ken Mackie N/A Bacterial and Virus Strains AAV5-CMV-fDIO-Cre-mNeonGreen-wPRE This paper VB180530-1030aad rAAV2-CAG-tdTomato ( Chan et al., 2017 ) RRID: Addgene_59462 AAV5-CaMKII-ChR2(H134R)-eYFP-wPRE ( Lee et al., 2010 ) RRID: Addgene_26969 rAAV2-EF1a-mCherry-IRES-Flpo (Fenno et al., 2014) RRID: Addgene_55634 AAV5-CMV-Cre-eGFP-SV40 Gift from James M. Wilson RRID: Addgene_105545 rAAV2-pmSyn1-EBFP-Cre ( Madisen et al., 2015 ) RRID: Addgene_51507 AAV5-EF1a-DIO-ChR2(H134R)-eYFP-wPRE Gift from
Techniques: Virus, Recombinant, Software
Journal: Cell reports
Article Title: A TAZ-AXL-ABL2 feed-forward signaling axis promotes lung adenocarcinoma brain metastasis
doi: 10.1016/j.celrep.2019.11.018
Figure Lengend Snippet: A) Representative images (day 30 post-injection) and B) analysis of brain metastasis-free survival (BMFS) in mice injected intracardially with PC9-pFuLT or pFuLT-Tet-TAZ4SA-expressing cells. Mice were given dox water for the duration of the study. Statistical analysis calculated by Log-rank (Mantel-Cox) test. Parental (n=13), TAZ4SA (n=17). C-D) Quantitative analysis (day 30 post-injection) of brain-metastatic index in mice injected intracardially with C) PC9-pFuLT (n=13) vs. PC9-pFuLT-Tet-TAZ4SA (n=17) or D) HCC4006-pFuLT (n=9) vs HCC4006-pFuLT-Tet-TAZ4SA (n=10) cells. Statistical analysis calculated by unpaired two-tailed t test. ** p-value < 0.01. E) Representative images of ex vivo mouse brains on day 32 post-injection with HCC4006-pFuLT or HCC4006-Tet-TAZ4SA cells. F) Diagram of iterative derivation of brain-metastatic cell lines. G) GSEA plot of TAZ4SA signature in PC9 parental vs PC9-BrM3 RNA-seq dataset. NES=normalized enrichment score. H) Venn diagram of overlapping transcripts upregulated in PC9-BrM3 and PC9-TAZ4SA cells. I) Representative images (day 42 post-injection) and J) BMFS in mice injected intracardially with PC9-BrM3 cells expressing non-target control (shNTC, n=10) or shTAZ (clone #73, n=10). K) Immunoblot to evaluate TAZ shRNA knockdown in PC9-BrM3 cells. Actin was used for protein loading control.
Article Snippet: Recombinant DNA & Plasmids pLKO-puro Non-Target shRNA Control Sigma Mission TRC1 SHC016-1EA pLKO-puro shAXL 1040 Sigma Mission TRC1 TRCN0000001040 pLKO-puro shTAZ 70 Sigma Mission TRC1 TRCN0000019470 pLKO-puro shTAZ 71 Sigma Mission TRC1 TRCN0000019471 pLKO-puro shTAZ 73 Sigma Mission TRC1 TRCN0000019473 TetO-FUW-pgk-puro ( Chowdhury et al., 2016 ) Addgene #85747; RRID:Addgene_85747 pLVX-Tight-Puro Tet-On Vector Xaralabos Varelas, Boston University, Boston, MA, USA N/A pLVX-TP-3F-TAZ4SA Xaralabos Varelas, Boston University, Boston, MA, USA
Techniques: Injection, Expressing, Two Tailed Test, Ex Vivo, RNA Sequencing, Control, Western Blot, shRNA, Knockdown
Journal: Cell reports
Article Title: A TAZ-AXL-ABL2 feed-forward signaling axis promotes lung adenocarcinoma brain metastasis
doi: 10.1016/j.celrep.2019.11.018
Figure Lengend Snippet: KEY RESOURCES TABLE
Article Snippet: Recombinant DNA & Plasmids pLKO-puro Non-Target shRNA Control Sigma Mission TRC1 SHC016-1EA pLKO-puro shAXL 1040 Sigma Mission TRC1 TRCN0000001040 pLKO-puro shTAZ 70 Sigma Mission TRC1 TRCN0000019470 pLKO-puro shTAZ 71 Sigma Mission TRC1 TRCN0000019471 pLKO-puro shTAZ 73 Sigma Mission TRC1 TRCN0000019473 TetO-FUW-pgk-puro ( Chowdhury et al., 2016 ) Addgene #85747; RRID:Addgene_85747 pLVX-Tight-Puro Tet-On Vector Xaralabos Varelas, Boston University, Boston, MA, USA N/A pLVX-TP-3F-TAZ4SA Xaralabos Varelas, Boston University, Boston, MA, USA
Techniques: Western Blot, Immunofluorescence, Recombinant, In Vivo, In Vitro, Mutagenesis, Caspase-Glo Assay, RNA Sequencing, shRNA, Control, Plasmid Preparation, Software