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弥漫性肺泡损伤中的巨核细胞与血小板稳态

Megakaryocytes and platelet homeostasis in diffuse alveolar damage.

作者信息

Mandal Rajni V, Mark Eugene J, Kradin Richard L

机构信息

Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.

出版信息

Exp Mol Pathol. 2007 Dec;83(3):327-31. doi: 10.1016/j.yexmp.2007.08.005. Epub 2007 Aug 31.

Abstract

Platelet homeostasis reflects a balance between the production of platelets via cytoplasmic fragmentation of megakaryocytes in the pulmonary microvasculature and their catabolism. Increased numbers of megakaryocytes are entrapped in the injured lung, potentially affecting circulating platelet counts. We enumerated pulmonary megakaryocytes and blood platelets in patients with diffuse alveolar damage (DAD) in order to determine their association with clinical outcome. Lung biopsies were examined from 21 patients with histologically documented DAD in its proliferative phase and secondary to a variety of causes. Blood platelet counts were determined within 24 h prior to lung biopsy, and CD61+ pulmonary megakaryocytes were localized in in situ immunohistochemical stains. The overall mortality in this series was 67%. Patients with DAD attributable to drug toxicity (DAD-D) had higher mortality (80%) and greater number of intrapulmonary CD61+ megakaryocytes than those with DAD due to other causes (23+/-7, 10+/-2, p<0.05). Patients with blood platelet counts =350 th/cm(3) showed increased survival (p<0.05). The findings support the hypothesis that abnormal platelet homeostasis is associated with increased mortality in acute lung injury and indicate that thrombocytosis in ARDS is associated with improved survival. The mechanisms of altered platelet homeostasis in DAD merit further investigation.

摘要

血小板稳态反映了肺微血管中巨核细胞通过细胞质分裂产生血小板与其分解代谢之间的平衡。数量增多的巨核细胞被困在受损肺中,这可能会影响循环血小板计数。我们对弥漫性肺泡损伤(DAD)患者的肺巨核细胞和血小板进行了计数,以确定它们与临床结局的关联。对21例组织学确诊处于增殖期且病因多样的DAD患者的肺活检组织进行了检查。在肺活检前24小时内测定血小板计数,并通过原位免疫组化染色定位CD61 +肺巨核细胞。该系列患者的总死亡率为67%。药物毒性所致DAD(DAD-D)患者的死亡率较高(80%),肺内CD61 +巨核细胞数量比其他病因所致DAD患者更多(分别为23±7、10±2,p<0.05)。血小板计数=350×10⁹/L的患者生存率有所提高(p<0.05)。这些发现支持了以下假设:血小板稳态异常与急性肺损伤死亡率增加相关,并表明ARDS中的血小板增多症与生存率提高相关。DAD中血小板稳态改变的机制值得进一步研究。

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