4.7 Article

BECLIN1 Is Essential for Podocyte Secretory Pathways Mediating VEGF Secretion and Podocyte-Endothelial Crosstalk

期刊

出版社

MDPI
DOI: 10.3390/ijms23073825

关键词

podocyte; BECLIN1; autophagy; secretory pathway; Golgi network; VEGF; glomerulosclerosis

资金

  1. German Research Foundation (Deutsche Forschungsgemeinschaft, DFG) [CRC 992, CRC 1192, KR1984/1, KR1984/4-1]
  2. European Research Council [616891]
  3. H2020-IMI2 consortium BEAt-DKD (Biomarker Enterprise to Attack Diabetic Kidney Disease) [115974]
  4. STOP-FSGS (Speed Translation-Oriented Progress to Treat Focal Segmental Glomerulosclerosis) [01GM1901C]
  5. National Natural Science Foundation of China [81470912]
  6. Alexander von Humboldt Foundation
  7. Uehara Memorial Foundation
  8. Berta Ottenstein Programm
  9. Else Kroner-Fresenius-Stiftung
  10. NAKSYS
  11. iPRIME
  12. European Research Council (ERC) [616891] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

This study demonstrates the importance of a secretory pathway for podocyte integrity and function, and identifies the key role of BECLIN1 in this process. By promoting VEGFA secretion, BECLIN1 maintains endothelial integrity within the glomerular filtration barrier.
Vascular endothelial growth factor A (VEGFA) secretion from podocytes is crucial for maintaining endothelial integrity within the glomerular filtration barrier. However, until now, the molecular mechanisms underlying podocyte secretory function remained unclear. Through podocyte-specific deletion of BECLIN1 (ATG6 or Becn1), a key protein in autophagy initiation, we identified a major role for this molecule in anterograde Golgi trafficking. The Becn1-deficient podocytes displayed aberrant vesicle formation in the trans-Golgi network (TGN), leading to dramatic vesicle accumulation and complex disrupted patterns of intracellular vesicle trafficking and membrane dynamics. Phenotypically, podocyte-specific deletion of Becn1 resulted in early-onset glomerulosclerosis, which rapidly progressed and dramatically reduced mouse life span. Further, in vivo and in vitro studies clearly showed that VEGFA secretion, and thereby endothelial integrity, greatly depended on BECLIN1 availability and function. Being the first to demonstrate the importance of a secretory pathway for podocyte integrity and function, we identified BECLIN1 as a key component in this complex cellular process. Functionally, by promoting VEGFA secretion, a specific secretory pathway emerged as an essential component for the podocyte-endothelial crosstalk that maintains the glomerular filtration barrier.

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