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自身免疫性肺气肿的动物模型。

An animal model of autoimmune emphysema.

作者信息

Taraseviciene-Stewart Laimute, Scerbavicius Robertas, Choe Kang-Hyeon, Moore Melissa, Sullivan Andrew, Nicolls Mark R, Fontenot Andrew P, Tuder Rubin M, Voelkel Norbert F

机构信息

Department of Medicine, Division of Pulmonary Sciences, UCHSC, 4200 East Ninth Ave, C272, Denver, CO 80262, USA.

出版信息

Am J Respir Crit Care Med. 2005 Apr 1;171(7):734-42. doi: 10.1164/rccm.200409-1275OC. Epub 2004 Nov 24.

Abstract

Although cigarette smoking is implicated in the pathogenesis of emphysema, the precise mechanisms of chronic progressive alveolar septal destruction are not well understood. We show, in a novel animal model, that immunocompetent, but not athymic, nude rats injected intraperitoneally with xenogeneic endothelial cells (ECs) produce antibodies against ECs and develop emphysema. Immunization with ECs also leads to alveolar septal cell apoptosis and activation of matrix metalloproteases MMP-9 and MMP-2. Anti-EC antibodies cause EC apoptosis in vitro and emphysema in passively immunized mice. Moreover, immunization also causes accumulation of CD4+ T cells in the lung. Adoptive transfer of pathogenic, spleen-derived CD4+ cells into naive immunocompetent animal also results in emphysema. This study shows for the first time that humoral- and CD4+ cell-dependent mechanisms are sufficient to trigger the development of emphysema, suggesting that alveolar septal cell destruction might result from immune mechanisms.

摘要

尽管吸烟与肺气肿的发病机制有关,但慢性进行性肺泡间隔破坏的确切机制尚未完全清楚。我们在一种新型动物模型中发现,具有免疫活性而非无胸腺的裸鼠腹腔注射异种内皮细胞(ECs)后会产生抗ECs抗体并发展为肺气肿。用ECs免疫还会导致肺泡间隔细胞凋亡以及基质金属蛋白酶MMP-9和MMP-2的激活。抗EC抗体在体外可导致EC凋亡,并使被动免疫的小鼠发生肺气肿。此外,免疫还会导致肺中CD4+T细胞的积聚。将致病性的、源自脾脏的CD4+细胞过继转移到未接触过抗原的具有免疫活性的动物体内也会导致肺气肿。这项研究首次表明,体液和CD4+细胞依赖性机制足以引发肺气肿的发展,提示肺泡间隔细胞破坏可能是由免疫机制导致的。

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