4.7 Article

Spatio-temporal expression pattern and role of the tight junction protein MarvelD3 in pancreas development and function

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SCIENTIFIC REPORTS
卷 11, 期 1, 页码 -

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NATURE RESEARCH
DOI: 10.1038/s41598-021-93654-2

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资金

  1. Fonds Speciaux de Recherche-UCLouvain (FSR)
  2. Actions de Recherche concertees-UCLouvain [ARC 10/15, ARC 15/20-065]
  3. Fonds pour la Recherche Scientifique (F.R.S-FNRS, Belgium) [3.4592.10, J.0126.16]
  4. Fondation Roi Baudouin
  5. Moorfields Eye Charity [GR001000]
  6. BBSRC [BB/J015032/1]
  7. Televie (F.R.S-FNRS, Belgium)
  8. de Duve Institute
  9. FSR (UCLouvain)
  10. BBSRC [BB/J015032/1] Funding Source: UKRI

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MarvelD3, an important tight junction protein expressed in adult epithelial and endothelial cells, was found to be involved in regulating cell behavior and survival through the MEKK1-JNK pathway. However, genetic ablation of MarvelD3 in mice did not significantly alter pancreatic tissue development and differentiation, suggesting that MarvelD3 may not be as crucial for these processes as previously thought.
Tight junction complexes are involved in the establishment and maintenance of cell polarity and the regulation of signalling pathways, controlling biological processes such as cell differentiation and cell proliferation. MarvelD3 is a tight junction protein expressed in adult epithelial and endothelial cells. In Xenopus laevis, MarvelD3 morphants present differentiation defects of several ectodermal derivatives. In vitro experiments further revealed that MarvelD3 couples tight junctions to the MEKK1-JNK pathway to regulate cell behaviour and survival. In this work, we found that MarvelD3 is expressed from early developmental stages in the exocrine and endocrine compartments of the pancreas, as well as in endothelial cells of this organ. We thoroughly characterized MarvelD3 expression pattern in developing pancreas and evaluated its function by genetic ablation. Surprisingly, inactivation of MarvelD3 in mice did not alter development and differentiation of the pancreatic tissue. Moreover, tight junction formation and organization, cell polarization, and activity of the JNK-pathway were not impacted by the deletion of MarvelD3.

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