mediated cell adhesion causes a delay in the early Biology Diagrams

mediated cell adhesion causes a delay in the early Biology Diagrams Experimental manipulations that strengthened FAs increased cell spreading and inhibited the G2/M transition, whereas reducing adhesion rescued the mitotic delay in DEPDC1B-KD cells. DEPDC1B was not necessary for normal cell cycle progression in a strain of HeLa cells adapted to grow in suspension. During mitosis, cells become rounded and lose attachment to the substrate. Marchesi et al. show that DEPDC1B, a cell-cycle-regulated protein, binds to the focal-adhesion-associated receptor PTPRF, thus inhibiting RhoA activation and leading to dismantling of focal adhesions upon mitotic entry. DEPDC1B thus links mitotic progression to de-adhesion. Keywords: adhesion, integrin, cell cycle, mitosis, G2 phase. 1. Integrins. Cell adhesion to the ECM is mainly mediated by the integrin family of receptors, which sense the chemical and mechanical properties of the extracellular microenvironment and generate responses regulating many cellular functions, including cell proliferation [1,2]. These

To explore the dynamics of adhesion re-modeling that accompany changes in cell shape during passage through mitosis (reviewed by Ramkumar and Baum, 2016), we chose to image mitotic progression in an adherent, migratory, diploid human cell line: RPE1-hTERT cells (Bodnar et al., 1998), which are widely used to study the cell cycle, cell division

Connections between the cell cycle, cell adhesion and the ... Biology Diagrams

Most adherent animal cells undergo drastic morphological changes upon entry into mitosis, beginning with the disassembly of cell adhesion to the extracellular matrix (ECM) and progressing with the Initial biochemical studies investigating the link between cell cycle and adhesion remodeling focused on mapping changes in phosphorylation of focal adhesion signaling layer proteins FAK, p130Cas and paxillin during mitosis [19,20]. How these changes were linked to cell cycle progression however was unclear. During mitosis, some interphase functions are retained, but the architecture of the cytoskeleton changes dramatically, and there is a need to generate a mitotic spindle for chromosome segregation. adhesion signalling and cell proliferation, particularly in the contexts of normal growth control and aberrant tumour progression. As the

Adhesion to the extracellular matrix persists during mitosis in most cell types. However, while classical adhesion complexes, such as focal adhesions, do and must disassemble to enable mitotic