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The intestinal epithelial lining rapidly renews every 4 to 5 days. The renewal is facilitated by intestinal stem cells (ISCs) located at the base of the crypt– a gland located at the bottom of each villus. ISCs divide asymmetrically to form new stem cells and progenitor daughter cells. The daughter cells are called transit-amplifying (TA) cells which move upwards along the crypt and either differentiate into absorptive cells– the enterocytes or secretory cells– including the...
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YAP1/TAZ Mediates Rumen Epithelial Cell Proliferation but Not Short-Chain Fatty Acid Metabolism In Vitro.

Bin Yang1,2,3, Zebang Xu2,3, Hongwei Chen2,3

  • 1School of Biological and Chemical Engineering, Zhejiang University of Science and Technology, Hangzhou 310023, China.

Animals : an Open Access Journal From MDPI
|March 28, 2024
PubMed
Summary

Yes1-associated protein (YAP1) and WW domain-containing transcription regulator protein 1 (TAZ) promote rumen epithelial cell proliferation. However, these key regulators do not influence sodium butyrate-induced rumen development or short-chain fatty acid metabolism.

Keywords:
GA-017YAP1/TAZproliferationrumen epithelial cellsodium butyrateverteporfin

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Area of Science:

  • Ruminant physiology
  • Molecular biology
  • Cellular signaling

Background:

  • Rumen development is crucial for ruminant health and growth.
  • Yes1-associated protein (YAP1) and WW domain-containing transcription regulator protein 1 (TAZ) are vital for mammalian epithelial regulation.
  • Understanding YAP1/TAZ roles in rumen epithelium is key for improving animal agriculture.

Purpose of the Study:

  • To investigate the impact of YAP1/TAZ on rumen epithelial (RE) cell proliferation.
  • To determine if YAP1/TAZ signaling mediates rumen development induced by sodium butyrate (SB).
  • To explore the relationship between YAP1/TAZ, Hippo, Wnt, and calcium signaling pathways in RE cells.

Main Methods:

  • Utilized GA-017 (GA) to activate YAP1/TAZ and verteporfin (VP) to inhibit YAP1/TAZ in RE cells.
  • Assessed RE cell proliferation and gene expression changes.
  • Investigated the effects of SB on RE cells with and without YAP1/TAZ modulation.

Main Results:

  • GA enhanced RE cell proliferation, while VP inhibited it, indicating YAP1/TAZ's role in proliferation.
  • YAP1/TAZ activation altered Hippo, Wnt, and calcium signaling pathways, increasing CCN1/2 expression.
  • YAP1/TAZ inhibition decreased BIRC3 expression.
  • SB treatment promoted RE cell differentiation and short-chain fatty acid (SCFA) metabolism gene expression, independent of YAP1/TAZ activity.

Conclusions:

  • YAP1/TAZ are potential targets for regulating RE cell proliferation.
  • YAP1/TAZ do not appear to mediate SB-induced RE development or SCFA metabolism.
  • SB does not affect YAP1/TAZ activity, suggesting distinct regulatory mechanisms in RE development.