4.5 Review Book Chapter

Terminal Differentiation in Epithelia: The Role of Integrins in Hensin Polymerization

Journal

ANNUAL REVIEW OF PHYSIOLOGY, VOL 73
Volume 73, Issue -, Pages 401-412

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev-physiol-012110-142253

Keywords

DMBT1; intercalated cells; acid-base

Categories

Funding

  1. NIDDK NIH HHS [DK20999] Funding Source: Medline
  2. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R37DK020999, R01DK020999] Funding Source: NIH RePORTER

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Epithelia, the most abundant cell type, differentiate to protoepithelia from stem cells by developing apical and basolateral membrane domains and form sheets of cells connected by junctions. Following this differentiation step, the cells undergo a second step (terminal differentiation), during which they acquire a mature phenotype, which unlike the protoepithelial one is tissue and organ specific. An extracellular matrix (ECM) protein termed hensin (DMBT1) mediates this differentiation step in the kidney intercalated cells. Although hensin is secreted as a soluble monomer, it requires polymerization and deposition in the ECM to become active. The polymerization step is mediated by the activation of inside-out signaling by integrins and by the secretion of two proteins: cypA (a cis-trans prolyl isomerase) and galectin 3.

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