RSS-Feed abonnieren
DOI: 10.1055/s-0038-1645970
Platelet Adhesion to Native Collagens Involves Proteoglycans and May Be a Two-Step Process
Publikationsverlauf
Received 27. Januar 1987
Accepted after revision 04. Mai 1987
Publikationsdatum:
27. Juni 2018 (online)
Summary
Adhesion of rat blood platelets to native rat tail collagen fibrils was studied in the electron microscope under conditions that preserved collagen-associated proteoglycans (CAPG). The CAPG molecules were aligned in chain-like configurations that encircled the fibrils with a 65 nm period; they appeared to coat the fibrils completely and extended 60-100 nm away from the fibril. The initial platelet-fibril contact occurred between the platelet glycocalyx and the CAPG of the fibrils i.e. between two surfaces with net-negative charges. When close contact was established between the fibril surface proper and the platelet membrane, CAPG were not identified in the area of contact, and the collagen-platelet distance was reduced to a ~10-12 nm wide gap traversed by delicate links in register with fibril periodicities.
-
References
- 1 Baumgartner HR, Muggli R. Adhesion and aggregation: morphological demonstration and quantitation in vivo and in vitro. In: Platelets in biology and pathology. Gordon JL. (ed.) Elsevier/North Holland Biomed Press; 1976. 1 23-60
- 2 Santoro SA, Cunningham LW. The interaction of platelets with collagen. In: Platelets in biology and pathology. Gordon JL. (ed.) Elsevier/North Holland Biomed Press; 1981. 2 249-264
- 3 Packham MA, Mustard JF. Platelet adhesion. Progr Hemostas Thrombos 1984; 7: 211-288
- 4 Scott JE. Collagen-proteoglycan interactions. Localization of proteoglycans in tendon by electron microscopy. Biochem J 1980; 187: 887-891
- 5 Behnke O, Zelander T. Preservation of intercellular substances by the cationic dye alcian blue in preparative procedures for electron microscopy. J Ultrastruct Res 1970; 31: 424-438
- 6 Nakao K, Bashey RI. Fine structure of collagen fibrils as revealed by ruthenium red. Exp Molec Pathol 1972; 17: 6-13
- 7 Myers DB, Highton TC, Rayns DG. Ruthenium red-positive filaments interconnecting collagen fibrils. J Ultrastruct Res 1973; 42: 87-92
- 8 Wight TN, Ross R. Proteoglycans in primate arteries. I. Ultrastructural localization and distribution in the intima. J Cell Biol 1975; 67: 660-574
- 9 Behnke O, Tranum-Jensen J. Specialized membrane areas in nonactivated and thrombin-activated platelets. Scand J Haematol 1986; 37: 203-209
- 10 Walsh PN. Platelet washing by albumin density gradient separation (ADGS). Adv Exp Med Biol 1972; 34: 245-256
- 11 Sheppard BL, French JE. Platelet adhesion in the rabbit abdominal aorta following the removal of the endothelium: a scanning and transmission electron microscopical study. Proc Roy Soc Lond B 1971; 176: 427-432
- 12 Phillips DR. An evaluation of membrane glycoproteins in platelet adhesion and aggragation. Progr Hemostas Thrombos 1980; 5: 81-109
- 13 Ward JV, Packham MA. Characterization of the sulfated gly-cosaminoglycan on the surface and in the storage granules of rabbit platelets. Biochim Biophys Acta 1979; 583: 196-207
- 14 Okayama M, Oguri K, Fujiwara Y, Nakanishi H, Yonekura H, Kondo T, Ui N. Purification and characterization of human platelet proteoglycan. Biochem J 1986; 233: 73-81
- 15 Handin RI, Cohen HJ. Purification and binding properties of human platelet factor 4. J Biol Chem 1976; 251: 4273-4278
- 16 Loscalzo J, Melnick B, Handin RI. The interaction of platelet factor four and glycosaminoglycans. Arch Biochem Biophys 1985; 240: 446-455
- 17 Goldberg ID, Stemerman MB, Handin RI. Vascular permeation of platelet factor 4 after endothelial injury. Science 1980; 209: 611-612
- 18 Sander HJ, Slot JW, Bouma BN, Bolhuis PA, Pepper DS, Sixma JJ. Immunocytochemical localization of fibrinogen, platelet factor 4, and beta thromboglobulin in thin frozen sections of human blood platelets. J Clin Invest 1983; 72: 12277-12287
- 19 Ginsberg MH, Taylor L, Painter RG. The mechanism of thrombin-induced platelet factor 4 secretion. Blood 1980; 55: 661-668