4.8 Article

Tyrosine kinase-mediated axial motility of basal cells revealed by intravital imaging

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NATURE COMMUNICATIONS
卷 7, 期 -, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/ncomms10666

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  1. NCI NIH HHS [P50 CA086355, P50CA086355] Funding Source: Medline
  2. NCRR NIH HHS [S10 RR031563, S10 RR031563-01, S10RR0266360] Funding Source: Medline
  3. NICHD NIH HHS [R01 HD040793, HD040793] Funding Source: Medline
  4. NIDDK NIH HHS [DK097124, DK43351, P30 DK043351, R01 DK097124, P30 DK057521, DK57521] Funding Source: Medline

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Epithelial cells are generally considered to be static relative to their neighbours. Basal cells in pseudostratified epithelia display a single long cytoplasmic process that can cross the tight junction barrier to reach the lumen. Using in vivo microscopy to visualize the epididymis, a model system for the study of pseudostratified epithelia, we report here the surprising discovery that these basal cell projections-which we call axiopodia-periodically extend and retract over time. We found that axiopodia extensions and retractions follow an oscillatory pattern. This movement, which we refer to as periodic axial motility (PAM), is controlled by c-Src and MEK1/2-ERK1/2. Therapeutic inhibition of tyrosine kinase activity induces a retraction of these projections. Such unexpected cell motility may reflect a novel mechanism by which specialized epithelial cells sample the luminal environment.

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