Platelet-derived growth factor β receptor regulates interstitial fluid homeostasis through phosphatidylinositol-3′ kinase signaling

Rainer Heuchel, Ansgar Berg, Michelle Tallquist, Karina Åhlén, Rolf K. Reed, Kristofer Rubin, Lena Claesson-Welsh, Carl Henrik Heldin, Philippe Soriano

Research output: Contribution to journalArticlepeer-review

162 Scopus citations

Abstract

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-β 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.

Original languageEnglish
Pages (from-to)11410-11415
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume96
Issue number20
DOIs
StatePublished - 28 Sep 1999
Externally publishedYes

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