» Articles » PMID: 18483217

Role of Platelet-derived Growth Factors in Physiology and Medicine

Overview
Journal Genes Dev
Specialty Molecular Biology
Date 2008 May 17
PMID 18483217
Citations 1066
Authors
Affiliations
Soon will be listed here.
Abstract

Platelet-derived growth factors (PDGFs) and their receptors (PDGFRs) have served as prototypes for growth factor and receptor tyrosine kinase function for more than 25 years. Studies of PDGFs and PDGFRs in animal development have revealed roles for PDGFR-alpha signaling in gastrulation and in the development of the cranial and cardiac neural crest, gonads, lung, intestine, skin, CNS, and skeleton. Similarly, roles for PDGFR-beta signaling have been established in blood vessel formation and early hematopoiesis. PDGF signaling is implicated in a range of diseases. Autocrine activation of PDGF signaling pathways is involved in certain gliomas, sarcomas, and leukemias. Paracrine PDGF signaling is commonly observed in epithelial cancers, where it triggers stromal recruitment and may be involved in epithelial-mesenchymal transition, thereby affecting tumor growth, angiogenesis, invasion, and metastasis. PDGFs drive pathological mesenchymal responses in vascular disorders such as atherosclerosis, restenosis, pulmonary hypertension, and retinal diseases, as well as in fibrotic diseases, including pulmonary fibrosis, liver cirrhosis, scleroderma, glomerulosclerosis, and cardiac fibrosis. We review basic aspects of the PDGF ligands and receptors, their developmental and pathological functions, principles of their pharmacological inhibition, and results using PDGF pathway-inhibitory or stimulatory drugs in preclinical and clinical contexts.

Citing Articles

Imatinib on target in stroke recovery.

Kwon H, Olson L J Clin Invest. 2025; 135(5).

PMID: 40026253 PMC: 11870721. DOI: 10.1172/JCI190024.


Brain pericytes and perivascular fibroblasts are stromal progenitors with dual functions in cerebrovascular regeneration after stroke.

Bernier L, Hefendehl J, Scott R, Tung L, Lewis C, Soliman H Nat Neurosci. 2025; 28(3):517-535.

PMID: 39962273 DOI: 10.1038/s41593-025-01872-y.


Chronotype and Cancer: Emerging Relation Between Chrononutrition and Oncology from Human Studies.

Godos J, Currenti W, Ferri R, Lanza G, Caraci F, Frias-Toral E Nutrients. 2025; 17(3).

PMID: 39940387 PMC: 11819666. DOI: 10.3390/nu17030529.


NexGen regen? Challenges and opportunities for growth factors and signaling agents in periodontal regeneration at intrabony defects.

Geisinger M Front Dent Med. 2025; 4:1239149.

PMID: 39916925 PMC: 11797756. DOI: 10.3389/fdmed.2023.1239149.


Hsa_circ_0001304 promotes vascular neointimal hyperplasia accompanied by autophagy activation.

Mu S, Lin J, Wang Y, Yang L, Wang S, Wang Z Commun Biol. 2025; 8(1):146.

PMID: 39881153 PMC: 11779959. DOI: 10.1038/s42003-025-07580-4.


References
1.
Majesky M, Daemen M, Schwartz S . Alpha 1-adrenergic stimulation of platelet-derived growth factor A-chain gene expression in rat aorta. J Biol Chem. 1990; 265(2):1082-8. View

2.
Raines E, Lane T, Iruela-Arispe M, Ross R, Sage E . The extracellular glycoprotein SPARC interacts with platelet-derived growth factor (PDGF)-AB and -BB and inhibits the binding of PDGF to its receptors. Proc Natl Acad Sci U S A. 1992; 89(4):1281-5. PMC: 48433. DOI: 10.1073/pnas.89.4.1281. View

3.
Bonner J . Regulation of PDGF and its receptors in fibrotic diseases. Cytokine Growth Factor Rev. 2004; 15(4):255-73. DOI: 10.1016/j.cytogfr.2004.03.006. View

4.
Hammes H, Lin J, Renner O, Shani M, Lundqvist A, Betsholtz C . Pericytes and the pathogenesis of diabetic retinopathy. Diabetes. 2002; 51(10):3107-12. DOI: 10.2337/diabetes.51.10.3107. View

5.
Kelly J, Sanchez A, Brown G, Chesterman C, Sleigh M . Accumulation of PDGF B and cell-binding forms of PDGF A in the extracellular matrix. J Cell Biol. 1993; 121(5):1153-63. PMC: 2119689. DOI: 10.1083/jcb.121.5.1153. View