Borok Z, Hami A, Danto S I, Zabski S M, Crandall E D
Will Rogers Institute Pulmonary Research Center, Division of Pulmonary and Critical Care Medicine, University of Southern California, Los Angeles 90033.
Am J Respir Cell Mol Biol. 1995 Jan;12(1):50-5. doi: 10.1165/ajrcmb.12.1.7811470.
Serum contains a number of polypeptide growth factors, hormones, and soluble matrix components and may influence the state of differentiation of epithelial cells in general and of alveolar epithelial cells (AEC) in particular. To evaluate the influence of sera on the transition from the type II toward the type I cell phenotype, we compared the effects of newborn bovine serum (NBS) and rat serum (RS) on morphologic changes and expression of a type I cell-specific epitope in AEC monolayers with time in primary culture. Rat type II AEC were harvested and cultured in defined serum-free medium (MDSF), MDSF + RS (5%), or MDSF + NBS (10%). Monolayer integrity was monitored by measuring transepithelial resistance (approximately 2,000 omega.cm2) and short-circuit current (approximately 4 microA/cm2). Binding of the type I cell-specific monoclonal antibody VIIIB2 was assessed between day 1 and day 11 by cell-based enzyme-linked immunosorbent assay (ELISA) and by immunoelectron microscopy (IEM). By ELISA, in MDSF and MDSF + NBS, VIIIB2 binding increased markedly after day 2, rising approximately 4-fold by day 8 (compared with day 1). In dramatic contrast, there was essentially no increase in VIIIB2 binding through day 11 in MDSF + RS. Results from IEM for apical surface binding of VIIIB2 were similar to those obtained by ELISA. Some morphologic differences were also noted, with cells in MDSF + RS being somewhat less spread at later times than those in MDSF or MDSF + NBS. These data indicate that the rate of rat type II AEC differentiation toward the type I cell phenotype is significantly modulated by soluble factor(s) present in rat serum.
血清含有多种多肽生长因子、激素和可溶性基质成分,可能会影响上皮细胞的分化状态,尤其是肺泡上皮细胞(AEC)的分化状态。为了评估血清对II型向I型细胞表型转变的影响,我们比较了新生牛血清(NBS)和大鼠血清(RS)对原代培养的AEC单层细胞形态变化和I型细胞特异性表位表达随时间的影响。收获大鼠II型AEC并在限定的无血清培养基(MDSF)、MDSF + RS(5%)或MDSF + NBS(10%)中培养。通过测量跨上皮电阻(约2,000Ω·cm2)和短路电流(约4μA/cm2)监测单层细胞的完整性。在第1天至第11天期间,通过基于细胞的酶联免疫吸附测定(ELISA)和免疫电子显微镜(IEM)评估I型细胞特异性单克隆抗体VIIIB2的结合情况。通过ELISA检测,在MDSF和MDSF + NBS中,第2天后VIIIB2结合显著增加,到第8天增加约4倍(与第1天相比)。形成鲜明对比的是,在MDSF + RS中,直到第11天VIIIB2结合基本没有增加。VIIIB2顶端表面结合的IEM结果与ELISA结果相似。还注意到一些形态学差异,MDSF + RS中的细胞在后期比MDSF或MDSF + NBS中的细胞铺展程度稍低。这些数据表明,大鼠血清中存在的可溶性因子显著调节大鼠II型AEC向I型细胞表型的分化速率。