Piguet P F, Vesin C
Department of Pathology, University of Geneva, Switzerland.
Int J Exp Pathol. 1994 Oct;75(5):321-8.
Platelet trapping was explored during the course of bleomycin induced pulmonary fibrosis by the injection of indium-111 labelled platelets and by light and electron microscopy (EM) of the alveolar capillaries. An i.v. injection of bleomycin markedly increased the localization of labelled platelets in the lung (but not in other organs) for about 3 weeks. On day 7 after bleomycin injection, a significant increase in the number of platelets in contact with the alveolar endothelium was seen with EM. Platelet trapping was strongly correlated (P < 0.005) with collagen deposition when examined in mouse strains genetically susceptible (CBA, C57BL/10, BL10 A.2R), or resistant (Balb/c, BL10.D2, BL10.A), to bleomycin induced fibrosis. In addition, several treatments known to decrease bleomycin induced collagen deposition and synthesis, namely administration of antibodies against CD11a, CD11b, TNF-alpha and IL-1ra, also decreased platelet trapping. As evaluated by EM, anti CD11a mAb significantly decreased the number of platelets in contact with the alveolar endothelium. This study indicates that bleomycin induced pulmonary fibrosis is strongly correlated with platelet trapping and that platelets probably interact, via their CD11a, with the CD54 born by the alveolar endothelium.
通过注射铟 - 111标记的血小板以及对肺泡毛细血管进行光学显微镜和电子显微镜(EM)观察,研究了博来霉素诱导的肺纤维化过程中的血小板捕获情况。静脉注射博来霉素可使标记血小板在肺内(而非其他器官)的定位显著增加,持续约3周。在注射博来霉素后第7天,电子显微镜观察发现与肺泡内皮接触的血小板数量显著增加。在对博来霉素诱导的纤维化敏感(CBA、C57BL/10、BL10 A.2R)或抗性(Balb/c、BL10.D2、BL10.A)的小鼠品系中进行检查时,血小板捕获与胶原蛋白沉积密切相关(P < 0.005)。此外,几种已知可减少博来霉素诱导的胶原蛋白沉积和合成的治疗方法,即给予抗CD11a、CD11b、TNF-α和IL-1ra的抗体,也减少了血小板捕获。通过电子显微镜评估,抗CD11a单克隆抗体显著减少了与肺泡内皮接触的血小板数量。这项研究表明,博来霉素诱导的肺纤维化与血小板捕获密切相关,并且血小板可能通过其CD11a与肺泡内皮细胞表面的CD54相互作用。