Two burgeoning families of platelet factor 4-related proteins: mediators of the inflammatory response
- PMID: 2149646
Two burgeoning families of platelet factor 4-related proteins: mediators of the inflammatory response
Abstract
The inflammatory response involves the recruitment and activation of various types of cells from the systemic circulation and from local tissues. One important component of the inflammatory response is the activation of platelets at sites of tissue injury and inflammation. In particular, activated platelets release large amounts of two proteins, platelet factor 4 (PF4) and beta-thromboglobulin (beta TG), which mediate several inflammatory processes. Recently, many novel proteins that are structurally related to PF4 and beta TG have been identified. The PF4-related proteins are secreted by white blood cells, endothelial cells, and fibroblasts in response to various inflammatory and mitogenic stimuli. Like PF4, these proteins appear to be inflammatory response mediators; several of them are potent chemoattractants, activating agents, or mitogens for specific cell types that are involved in the inflammatory response. The study of PF4-related proteins provides new insight into the mechanisms of the immune response, and may result in the development of new therapeutic agents.
Similar articles
-
Mitogenic activation of human T cells induces two closely related genes which share structural similarities with a new family of secreted factors.J Immunol. 1989 Mar 1;142(5):1582-90. J Immunol. 1989. PMID: 2521882
-
Assessment of platelet activity as expressed by plasma levels of platelet factor 4 and beta-thromboglobulin in patients with chronic idiopathic urticaria.Exp Dermatol. 2005 Jul;14(7):515-8. doi: 10.1111/j.0906-6705.2005.00311.x. Exp Dermatol. 2005. PMID: 15946239
-
Selective PF4 release in vitro induced by heparin and related glycosaminoglycans (GAGs)--correlation with beta-TG release and platelet aggregation.Thromb Haemost. 1984 Feb 28;51(1):105-7. Thromb Haemost. 1984. PMID: 6202020
-
Chemokines, inflammation and the immune system.Ther Immunol. 1994 Aug;1(4):229-46. Ther Immunol. 1994. PMID: 7584498 Review.
-
[Free radicals and antioxidants: physiology, human pathology and therapeutic aspects (part II)].Therapie. 1998 Jul-Aug;53(4):315-39. Therapie. 1998. PMID: 9806002 Review. French.
Cited by
-
Application of Proteomics to Inflammatory Bowel Disease Research: Current Status and Future Perspectives.Gastroenterol Res Pract. 2019 Jan 15;2019:1426954. doi: 10.1155/2019/1426954. eCollection 2019. Gastroenterol Res Pract. 2019. PMID: 30774653 Free PMC article. Review.
-
Inhibition of endothelial cell proliferation by platelet factor-4 involves a unique action on S phase progression.J Cell Biol. 1994 Nov;127(4):1121-7. doi: 10.1083/jcb.127.4.1121. J Cell Biol. 1994. PMID: 7962072 Free PMC article.
-
Uncoupling of stem cell inhibition from monocyte chemoattraction in MIP-1alpha by mutagenesis of the proteoglycan binding site.EMBO J. 1996 Dec 2;15(23):6506-15. EMBO J. 1996. PMID: 8978677 Free PMC article.
-
Transcriptional activation of the CEF-4/9E3 cytokine gene by pp60v-src.Mol Cell Biol. 1992 Apr;12(4):1490-9. doi: 10.1128/mcb.12.4.1490-1499.1992. Mol Cell Biol. 1992. PMID: 1549106 Free PMC article.
-
Induction of early-response genes KC and JE by mycobacterial lipoarabinomannans: regulation of KC expression in murine macrophages by Lsh/Ity/Bcg (candidate Nramp).Infect Immun. 1994 Apr;62(4):1176-84. doi: 10.1128/iai.62.4.1176-1184.1994. Infect Immun. 1994. PMID: 8132324 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources
Miscellaneous