d'Ortho M P, Clerici C, Yao P M, Delacourt C, Delclaux C, Franco-Montoya M L, Harf A, Lafuma C
Unité U296 de l'Institut National de la Santé et de la Recherche Médicale, Faculté de Médecine, Créteil, France.
Am J Physiol. 1997 Sep;273(3 Pt 1):L663-75. doi: 10.1152/ajplung.1997.273.3.L663.
Type II pneumocytes are key cells of the alveolar epithelium. They lie on the alveolar basement membrane, which influences their phenotype and functions. We hypothesized that type II pneumocytes degrade basement membrane components by producing gelatinases, members of the matrix metalloproteinase family. To investigate this hypothesis, we used primary cultures of rat type II pneumocytes and cultures of the human A549 cell line. We found by zymography that 70-kDa gelatinase was present in media conditioned by these cells. This 70-kDa gelatinase was identified as gelatinase A by a Western blot, and the presence of its mRNA was demonstrated by reverse transcription-polymerase chain reaction. A 95-kDa gelatinase could be induced under certain conditions. Production of gelatinases may take place during the turnover of basement membranes, in physiological and in pathophysiological processes. This was suggested by the increase in production of both gelatinases that we observed after in vitro exposure to LPS or interleukin-1. The presence of tissue inhibitors of matrix metalloproteinase-1 and -2 was also demonstrated, suggesting that degradation of extracellular matrix by type II pneumocytes is tightly regulated.
II型肺泡上皮细胞是肺泡上皮的关键细胞。它们位于肺泡基底膜上,而肺泡基底膜会影响其表型和功能。我们推测II型肺泡上皮细胞通过产生明胶酶(基质金属蛋白酶家族成员)来降解基底膜成分。为了验证这一推测,我们使用了大鼠II型肺泡上皮细胞原代培养物和人A549细胞系培养物。通过酶谱法我们发现这些细胞培养上清中存在70 kDa的明胶酶。通过蛋白质印迹法将这种70 kDa的明胶酶鉴定为明胶酶A,并通过逆转录聚合酶链反应证实了其mRNA的存在。在某些条件下可诱导产生一种95 kDa的明胶酶。明胶酶的产生可能发生在基底膜更新过程中,包括生理和病理生理过程。这一点我们是通过体外暴露于脂多糖或白细胞介素-1后观察到的两种明胶酶产量增加而推测出来的。同时也证实了基质金属蛋白酶-1和-2的组织抑制剂的存在,这表明II型肺泡上皮细胞对细胞外基质的降解受到严格调控。