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Platelet-derived growth factor beta receptor regulates interstitial fluid homeostasis through phosphatidylinositol-3' kinase signaling

Heuchel, Rainer (author)
Ludwiginstitutet för Cancerforskning
Berg, Ansgar (author)
Tallquist, Michelle (author)
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Åhlén, Karina (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Reed, Rolf K (author)
Rubin, Kristofer (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Claesson-Welsh, Lena (author)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi
Heldin, Carl-Henrik (author)
Ludwiginstitutet för Cancerforskning
Soriano, Philippe (author)
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 (creator_code:org_t)
1999
1999
English.
In: Proc Natl Acad Sci U S A. ; 96:20, s. 11410-5
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Platelet-derived growth factor (PDGF) isoforms lead to mitogenic, survival, and chemotactic responses in a variety of mesenchymal cell types during development and in the adult. We have studied the importance of phosphatidylinositol-3' kinase (PI3K) signaling in these responses by mutating the PI3K-binding sites in the PDGF-beta receptor by gene targeting in embryonic stem cells. Homozygous mutant mice developed normally; however, cells derived from the mutants were less chemotactic and had largely lost their ability to contract collagen gels in response to PDGF. Injection of a mast cell degranulating agent in mice led to a decrease in interstitial fluid pressure resulting in edema formation. In contrast to wild-type mice, mutant mice were unable to normalize the pressure after treatment with PDGF. Taken together, these observations suggest a function for PDGF signaling through PI3K in interstitial fluid homeostasis by modulating the tension between cells and extracellular matrix structures.

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