Fig. 2. Fluorescent images indicating the cytoskeleton of human bone marrow-derived mesenchymal stem cells (hBMSCs) subjected to cyclic stretching. Fluorescent.

Slides:

Advertisements

Similar presentations

Mitochondria localize to both the front and the rear of neutrophils.

Advertisements

Scanning electron microscopy analysis of EGK-I to -V chick embryos.

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. 1. Overview of the nervous system of the adult S. roscoffensis.

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.

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. 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. 4. A primary screen based on scrape closure

Fig. 6. Cross-section of the stomach wall and spiral intestine of the embryo, stained with PAS. (A) Surface of the stomach wall (SW) and ingested material.

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. 4. BMP and nodal induce invasion of metastatic and radial growth phase melanoma cells in human epidermal skin reconstructs. BMP and nodal induce invasion.

Fig. 1. Mitochondrial internalization in cardiomyocytes.

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.

Fig. 4. The model of malate metabolism in fruit cells under different K level conditions. The model of malate metabolism in fruit cells under different.

Fig. 1. E-cadherin localizes in nano-scale clusters.

Fig. 4. Acentriolar mitotic spindle assembly

Fig. 1. Pigmentation and melanophore counts of rainbow trout parr and smolt caudal fins.Pigmentation of (A) parr and (B) smolt. Pigmentation and melanophore.

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

Fig. 1. Ovarian cancer spheroids can bud from a monolayer

Kinetics of induced and non-induced AR, and its relationship to cell death and motility. Kinetics of induced and non-induced AR, and its relationship to.

Fig. 4. Detection of dFMR1 mRNA in dFMRP granules by FISH

Formation of papilloma lesions in the UroIICre+Fgfr3+/K644EK-RasG12D/+ model. Formation of papilloma lesions in theUroIICre+Fgfr3+/K644EK-RasG12D/+model.

Fig. 5. Morphological changes of the N

Fig. 5. The bulk of Cep135 localizes distantly from Sas-6 and STIL

Fig. 6. Comparison of Plk4 with Sas-6 localization

Fig. 5. GFP fluorescence colocalization of Gcn5.

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. 3. Effect of substrate orientation on growth rate for bottom-dwelling tadpoles with similar oral configuration. Effect of substrate orientation on.

Fig. 6. STK35 KO mice show ovary defects.

BMP signalling is dispensable for early gastruloid patterning.

Fig. 6. Apical polarity of primitive endoderm cells on surface of embryoid bodies.Embryoid bodies were analyzed by immunofluorescence microscopy for GATA4.

Fig. 3. Overexpression of wild-type GFP-CPAP, but not GFP-CPAP-377EE (GFP-377EE), induces cilia formation and promotes the growth of cilia.CAD cells (A,B)

Fig. 1. Polarized F-actin cables in the Xenopus neural plate.

Effect of the plastid translation inhibitor Spec on LR development

Fig. 3. idefix mutant chromatophores contribute to a wild-type pattern in chimeric animals. idefix mutant chromatophores contribute to a wild-type pattern.

Colocalisation and influence on migration.

Fig. 1. Loss of PC following INT depletion

Folic acid increases apical junctional pMLCK localization in vivo

Fig. 2. Non-homogeneous subcellular distribution of Vangl2 along the anteroposterior axis. Non-homogeneous subcellular distribution of Vangl2 along the.

Fig. 8. Tracking details and coordinate systems.

Fig. 2. iPSCs produce functional osteoblasts.

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

Global cell proliferation replenishes epidermal cells.

Fig. 3. Representive still images of typical pelagic foraging behaviour of Australaisan gannets. Representive still images of typical pelagic foraging.

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)

Peroxisome speeds were slower in patient and control cells.

Fig. 2. Acetylation stiffens primary cilia.

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.

Expression of smc3 in whole-mount and cryosectioned regenerating fins

Fig. 3. Mean force and velocity during jumping

Fig. 1. Expression of a Ror-eGFP fusion protein under control of the endogenous Ror promoter in Drosophila embryos. Expression of a Ror-eGFP fusion protein.

mip120 null egg chambers have a condensed nurse cell DNA phenotype

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. 1. lgl interacts genetically with Argonaute 1 (AGO1) in the eye.

Fig. 7. Analysis of dFMRP kinetics in dFMRP granules by FRAP

Example of swimming trajectories from three groups of fish from three different weeks along with the extracted behavioral parameters. Example of swimming.

Subcellular distribution of Mst4 and aPKCι in in vivo enterocytes.

Presentation transcript:

Fig. 2. Fluorescent images indicating the cytoskeleton of human bone marrow-derived mesenchymal stem cells (hBMSCs) subjected to cyclic stretching. Fluorescent images indicating the cytoskeleton of human bone marrow-derived mesenchymal stem cells (hBMSCs) subjected to cyclic stretching. Stretch ration: 8%, cyclic frequency: 1 Hz. (A,B) The hBMSCs were cultured on the plane PDMS chamber before cyclic stretching (A) and after cyclic stretching for 48 h (B). The cells avoided the cyclic stretching by aligning nearly orthogonal to the stretch direction. (C) The quantitative result of the escape of the hBMSCs cultured on the plane PDMS chamber from the cyclic stretching. The cell orientation angle θ means an angle between the stretch direction and the longitudinal axis of each cell when the cells were considered as ellipses. (D,E) The hBMSCs were cultured on the aligned microgrooved PDMS chamber before cyclic stretching (D) and after cyclic stretching for 48 h (E). The microgrooves were aligned horizontally, and the cells were oriented along the direction of the microgrooves. Scale bars: (A,B) 100 µm, (D,E) 200 µm. Yasuyuki Morita et al. Biology Open 2019;8:bio039164 © 2019. Published by The Company of Biologists Ltd