Suppr超能文献

大鼠肺泡上皮细胞IV型胶原蛋白的产生

Type IV collagen production by rat pulmonary alveolar epithelial cells.

作者信息

Simon R H, Scott M J, Reza M M, Killen P D

机构信息

Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109.

出版信息

Am J Respir Cell Mol Biol. 1993 Jun;8(6):640-6. doi: 10.1165/ajrcmb/8.6.640.

Abstract

Maintenance and repair of the pulmonary alveolar basement membrane are critical processes for preserving normal alveolar structure and function. To elucidate the mechanisms that control type IV collagen production by pulmonary alveolar epithelial cells, type II pneumocytes from rat lungs were isolated and maintained in tissue culture as monolayers. Using Northern blot analysis and metabolic labeling, we found that the cultured epithelial cells express type IV collagen mRNA and incorporate [3H]proline into type IV collagen. To determine the effects of phenotype on control of type IV collagen synthesis, we took advantage of the well-described observation that isolated type II cells lose their distinctive type II features when cultured on plastic in serum-containing medium for 7 days and assume an appearance more like that of type I epithelial cells. We found that [3H]proline incorporation into type IV collagen increased from day 1 to day 2 and thereafter decreased gradually up to day 7. Despite this decrease in [3H]proline incorporation, type IV collagen mRNA increased over the same period. If the loss of type II cell characteristics was prevented by culturing the cells in EHS matrix, a basement membrane-like extracellular matrix, there was little increase in relative abundance of type IV collagen mRNA as compared with cells cultured on plastic. We therefore conclude that type IV collagen production by isolated pulmonary alveolar epithelial cells is controlled, at least in part, by translational or post-translational mechanisms. Furthermore, the full type II cell phenotype is not required for expression of type IV collagen genes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

肺泡基底膜的维持和修复是保持正常肺泡结构和功能的关键过程。为了阐明控制肺泡上皮细胞IV型胶原产生的机制,从大鼠肺中分离出II型肺细胞,并在组织培养中以单层形式维持。通过Northern印迹分析和代谢标记,我们发现培养的上皮细胞表达IV型胶原mRNA,并将[3H]脯氨酸掺入IV型胶原中。为了确定表型对IV型胶原合成控制的影响,我们利用了一个广为人知的观察结果,即分离的II型细胞在含血清培养基中于塑料上培养7天时会失去其独特的II型特征,并呈现出更类似于I型上皮细胞的外观。我们发现,从第1天到第2天,[3H]脯氨酸掺入IV型胶原的量增加,此后逐渐减少直至第7天。尽管[3H]脯氨酸掺入量有所下降,但IV型胶原mRNA在同一时期却增加了。如果通过在EHS基质(一种基底膜样细胞外基质)中培养细胞来防止II型细胞特征的丧失,与在塑料上培养的细胞相比,IV型胶原mRNA的相对丰度几乎没有增加。因此,我们得出结论,分离的肺泡上皮细胞产生IV型胶原至少部分受翻译或翻译后机制控制。此外,IV型胶原基因的表达不需要完整的II型细胞表型。(摘要截短至250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验