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表面活性蛋白A(SP-A)在人肺实质区域的细胞内及肺泡内定位

Intracellular and intraalveolar localization of surfactant protein A (SP-A) in the parenchymal region of the human lung.

作者信息

Ochs Matthias, Johnen Georg, Müller Klaus-Michael, Wahlers Thorsten, Hawgood Samuel, Richter Joachim, Brasch Frank

机构信息

Department of Anatomy, Division of Electron Microscopy, University of Göttingen, Göttingen, Germany.

出版信息

Am J Respir Cell Mol Biol. 2002 Jan;26(1):91-8. doi: 10.1165/ajrcmb.26.1.4570.

Abstract

Although it is clearly established that surfactant protein A (SP-A) is secreted by type II pneumocytes as a component of pulmonary surfactant, its secretion pathway as well as its subcellular localization in the human lung are uncertain. We therefore studied the intracellular and intra-alveolar localization of SP-A in eight adult human lungs by immunohistochemistry and immunoelectron microscopy. Only type II pneumocytes could be identified as SP-A positive cells within the parenchymal region. SP-A was localized mainly in small vesicles and multivesicular bodies close to the apical plasma membrane. Only few lamellar bodies were weakly labeled at their outer membranes. Stereologic analysis showed this weak signal to be due to specific labeling. In the alveolar space, lamellar body-like surfactant forms in close proximity to tubular myelin were labeled for SP-A at their periphery. The strongest SP-A labeling was found over tubular myelin figures. Labeling for SP-A was also found in close association with the surface film and unilamellar vesicles. Our results support the hypothesis that, in the human lung, SP-A is mainly secreted into the alveolar space via an alternative pathway that largely bypasses the lamellar bodies. After secretion, the outer membranes of unwinding lamellar bodies become enriched with SP-A when tubular myelin formation is initiated. SP-A may also be involved in the transition of tubular myelin into the surface film.

摘要

尽管表面活性蛋白A(SP-A)作为肺表面活性剂的一个组成部分由II型肺细胞分泌这一点已明确确立,但其分泌途径以及在人肺中的亚细胞定位仍不明确。因此,我们通过免疫组织化学和免疫电子显微镜研究了8例成人肺中SP-A的细胞内和肺泡内定位。在实质区域内,只有II型肺细胞可被鉴定为SP-A阳性细胞。SP-A主要定位于靠近顶端质膜的小泡和多囊体中。只有少数板层小体的外膜有微弱标记。体视学分析表明,这种微弱信号是特异性标记所致。在肺泡腔内,与管状髓磷脂紧邻的类似板层小体的表面活性物质形式在其周边被标记为SP-A。在管状髓磷脂结构上发现了最强的SP-A标记。在与表面膜和单层小泡紧密相关的部位也发现了SP-A标记。我们的结果支持这样一种假说,即在人肺中,SP-A主要通过一条很大程度上绕过板层小体的替代途径分泌到肺泡腔内。分泌后,当开始形成管状髓磷脂时,展开的板层小体的外膜富含SP-A。SP-A也可能参与管状髓磷脂向表面膜的转变。

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