Fig. 2. DDR1 over-expression enhances collagen fibril reorganization

Slides:



Advertisements
Similar presentations
SiRNA knockdown of dynein IC2-C recovered the inhibition of neurite outgrowth in NF1-KD PC12 cells. siRNA knockdown of dynein IC2-C recovered the inhibition.
Advertisements

CK2 is required for early cell divisions in C. elegans embryos
Aggregation is not required for cytoplasmic relocalization induced by misfolding mutations. Aggregation is not required for cytoplasmic relocalization.
Fig. 5. Prip silencing enhances the co-localization of GABARAP with insulin vesicles and β-tubulin.Co-localization of GABARAP (green) with insulin (red)
Fig. 3. Effect of NH4Cl (0 or 30 mM) on percentage of motile spermatozoa and VAP after 1 and 5 min after activation. Effect of NH4Cl (0 or 30 mM) on percentage.
Fig. 7. Vinculin recruitment enhances the efficiency of barrier formation.(A) TER measurements after a calcium switch in α-catenin-depleted MDCK cells.
Fig. 1. Representative images of the four cell lines using fluorescence microscopy. Representative images of the four cell lines using fluorescence microscopy.
VacA does not induce phosphorylation of Src in RPTPα constitutive-knockdown AZ-521 cells. VacA does not induce phosphorylation of Src in RPTPα constitutive-knockdown.
Fig. 1. Chlamydia infection causes elevated levels of sortilin.
Fig. 4. smc3 regulates the expression of cx43 in regenerating fins.
Fig. 2. Morphological changes of cultured adherent fibroblastic cells after OA treatment related to actin microfilament reorganization.(A) Cells observed.
Fig. 5. Differentiated cells sort to the outer layer, regardless of E- or N-cadherin status.Wildtype and mutant ES cells were distinguished by GFP expression.
Fig. 7. Motion adaptation increases time-dependent response modulations (TDRM) relatively to the average cell response.TDRM normalized to the value obtained.
Fig. 2. Proportion of motile objects and track length
Fig. 2. abu/pqn genes are expressed in the pharyngeal cuticle
Fig. 10. Ratiometric live imaging of di-4-ANEPPDHQ in growing pollen tubes.(A) Higher and lower membrane order distribution in control and BCD treated.
Fig. 7. Knockdown of Meis1 abolishes CR4. 2-GFP expression
Fig. 1. Mitochondrial internalization in cardiomyocytes.
Fig. 3. Read-outs of mTORC1 (P-S6(S235/236)) and mTORC2 (P-Akt(S473)) in wtPC12 and PC12-27 cells.(A,B) wtPC12 and PC12-27 cells were treated for 48 hr.
Fig. 1. Loss of PC following INT depletion
Fig. 1. Morphological and growth characterization of hBMCs and hPDCs
Fig. 2. Transfection and clonal selection of rat pluripotent stem cells to generate stable transgenic lines. Transfection and clonal selection of rat pluripotent.
Table 2. Cell surface abundance of β1 integrin measured by flow cytometry.DDR wild type and DDR over-expressing cells were treated with deoxymannojirimycin.
Fig. 1. E-cadherin localizes in nano-scale clusters.
Fig. 7. E2F1 acetylation in A1/A2-KO MEFs
Fig. 1. Ovarian cancer spheroids can bud from a monolayer
The initial targeting of Sec61b mRNA to the ER is partially dependent on ribosomes and translation. The initial targeting of Sec61b mRNA to the ER is partially.
Fig. 8. Knockdown of Meis1 reduces the expression of Foxn4 and Lim1+2
Fig. 3. Characterization of unclassified cells (UCs).
Differentiation of neural crest cells into corneal endothelial cells
Fig. 4. Detection of dFMR1 mRNA in dFMRP granules by FISH
Fig. 3. Coilin levels correlate with altered nascent U2 snRNA, hTR and rRNA levels.RNA isolated from HeLa or WI-38 cells following RNAi targeting coilin.
Fig. 5. The bulk of Cep135 localizes distantly from Sas-6 and STIL
Fig. 6. Comparison of Plk4 with Sas-6 localization
Fig. 2. The localisation of integrins β1 and α6 in the hES cells grown in a colony and as a single-cell culture. hES cells were harvested manually as small.
Fig. 7. Lhx1-RNAi reduces the eye size
Fig. 2. Centrosomal proteins display distinct localizations and radial distances from centriole walls.U2OS cells were fixed and stained with the indicated.
Fig. 3. Rnd proteins induce stronger responses in subconfluent endothelial cells.HUVECs were transfected with Rnd1, Rnd2, Rnd3 or GFP-encoding plasmids.
Fig. 7. Representative images of control (Cas9+GFP) and Cas9+gRNA+GFP co-injected embryos on day 4 of culture, showing nuclear-imported GFP (green) and.
Fig. 6. STK35 KO mice show ovary defects.
Fig. 2. Fluorescent images indicating the cytoskeleton of human bone marrow-derived mesenchymal stem cells (hBMSCs) subjected to cyclic stretching. Fluorescent.
Fig. 3. Weak interaction between E-cadherin and N-cadherin null cells
Fig. 2. Kinetics of OptoEphB2 activation.
Fig. 4. Expression analysis of Onecut transcription factors during mdDA neuron development.Adjacent coronal sections of E11.5, E12.5 and E13.5 mouse brains.
Abnormally low or high Tj expression causes a decrease in DEcad expression and shg enhancer activity. Abnormally low or high Tj expression causes a decrease.
EpiDEG efficiently degrades GFP-tagged proteins that localize to different subcellular localizations. epiDEG efficiently degrades GFP-tagged proteins that.
Fig. 3. Exogenous folic acid rescues neural epithelial apical constriction and activation of non-muscle myosin upon Rho-kinase inhibition. Exogenous folic.
Fig. 1. Loss of PC following INT depletion
Fig. 3. Enhanced EGFR signaling in Rhbdf2P159L/P159L mice.
N-cadherin deficient cells do not adhere or migrate.
Fig. 2. Analysis of morphology, pluripotency marker expression and transgene silencing in the colonies emerging during reprogramming. Analysis of morphology,
Folic acid increases apical junctional pMLCK localization in vivo
HEK-cFXN cells show a correlation among ROS levels, LIP and frataxin expression. HEK-cFXN cells show a correlation among ROS levels, LIP and frataxin expression.
Fig. 3. Effects of Tec on IL-1β-induced apoptosis in chondrocytes.
V-ATPase and proteins involved in late endosomal protein sorting are required for efficient utilization of LDs during growth resumption. V-ATPase and proteins.
Ibm1 and edm2 mutants generate more stomatal divisions in the leaf epidermis. ibm1 and edm2 mutants generate more stomatal divisions in the leaf epidermis.
dcn1-deletion results in attenuated cohesin cleavage at anaphase
Fig. 2. Effects of pH on percentage of motile spermatozoa and VAP after 1 and 5 min after activation. Effects of pH on percentage of motile spermatozoa.
Fig. 2. Expression of Cx43 mutant T154A resulted in non-radial spreading and formation of protrusions in J558µm3 cells spreading in response to BCR signaling.(A)
Fig. 4. CR4.2 may be active in amacrine cells but not in ganglion cells.Chick retinas were electroporated with either the control CAG-GFP construct or.
Fig. 1. Expression of the five miRNAs encoded by two miRNA clusters in mouse sperm and oocytes.(A) qPCR analyses of levels of miR-16 (positive control),
Fig. 1. Cell adhesion molecule expression and the aggregation of wildtype and mutant ES cells.(A) Wildtype (WT), E-cadherin null (9J), and N-cadherin null.
Fig. 1. Rnd2 and Rnd3 induce stress fibres whereas Rnd1 reduces stress fibres in endothelial cells.(A) Rnd mRNAs are expressed in HUVECs. Total RNA was.
The BRCA1 aggregates exclude large nuclear structures.
Depletion of COPI protein inhibits cis to trans cisternal maturation.
Fig. 5. Co-expression analyses of disease mutations in YFP-RPGRIP1α1 with wild-type RFP-RPGR1–19 or RFP-RPGRORF15 in COS7 cells.YFP-RPGRIP1α1 with disease-associated.
Fig. 5. Behaviours of the wild-types Oregon-R at two temperatures.
Fig. 4. Tetracycline-regulated expression of ClC-5 in the HEK293 cells stably expressing gastric H+,K+-ATPase.(A) Alignments of rat ClC-5, human ClC-5,
Effects of paclitaxel and vinblastine.
Aplf downregulation does not induce cellular arrest.
Presentation transcript:

Fig. 2. DDR1 over-expression enhances collagen fibril reorganization Fig. 2. DDR1 over-expression enhances collagen fibril reorganization.(A) Knockdown (KD), wild type (WT) or DDR1 over-expressing (OE) cells were cultured on FITC-labeled fibrillar collagen gels for 12 h (upper panel) or 24 h (lower panel) to evaluate morphologically, collagen remodeling. DDR1 over-expression enhances collagen fibril reorganization.(A) Knockdown (KD), wild type (WT) or DDR1 over-expressing (OE) cells were cultured on FITC-labeled fibrillar collagen gels for 12 h (upper panel) or 24 h (lower panel) to evaluate morphologically, collagen remodeling. Bar = 20 µm; (B) Quantification of FITC-collagen fluorescence in fixed area regions of interest by image analysis using Image J. Mean fluorescent intensity was obtained from average fluorescence intensities normalized to data of same gels without cells. At least 4 representative images were analyzed for each condition. Data are mean±standard errors of fluorescence intensity in arbitrary units (AU) in sampling grids. Lisa A. Staudinger et al. Biology Open 2013;bio.20135090 © 2013. Published by The Company of Biologists Ltd