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首页> 外文期刊>American Journal of Physiology >Modulation of t1alpha expression with alveolar epithelial cell phenotype in vitro.
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Modulation of t1alpha expression with alveolar epithelial cell phenotype in vitro.

机译:在体外用肺泡上皮细胞表型调节t1alpha表达。

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摘要

T1alpha is a recently identified gene expressed in the adult rat lung by alveolar type I (AT1) epithelial cells but not by alveolar type II (AT2) epithelial cells. We evaluated the effects of modulating alveolar epithelial cell (AEC) phenotype in vitro on T1alpha expression using either soluble factors or changes in cell shape to influence phenotype. For studies on the effects of soluble factors on T1alpha expression, rat AT2 cells were grown on polycarbonate filters in serum-free medium (MDSF) or in MDSF supplemented with either bovine serum (BS, 10%), rat serum (RS, 5%), or keratinocyte growth factor (KGF, 10 ng/ml) from either day 0 or day 4 through day 8 in culture. For studies on the effects of cell shape on T1alpha expression, AT2 cells were plated on thick collagen gels in MDSF supplemented with BS. Gels were detached on either day 1 (DG1) or day 4 (DG4) or were left attached until day 8. RNA and protein were harvested at intervals between days 1 and 8 in culture, and T1alpha expression was quantified by Northern and Western blotting, respectively. Expression of T1alpha progressively increases in AEC grown in MDSF +/- BS between day 1 and day 8 in culture, consistent with transition toward an AT1 cell phenotype. Exposure to RS or KGF from day 0 prevents the increase in T1alpha expression on day 8, whereas addition of either factor from day 4 through day 8 reverses the increase. AEC cultured on attached gels express high levels of T1alpha on days 4 and 8. T1alpha expression is markedly inhibited in both DG1 and DG4 cultures, consistent with both inhibition and reversal of the transition toward the AT1 cell phenotype. These results demonstrate that both soluble factors and alterations in cell shape modulate T1alpha expression in parallel with AEC phenotype and provide further support for the concept that transdifferentiation between AT2 and AT1 cell phenotypes is at least partially reversible.
机译:T1alpha是最近鉴定的成年大鼠肺中由I型肺泡(AT1)上皮细胞表达的基因,而不是由II型肺泡(AT2)上皮细胞表达的基因。我们使用可溶性因子或改变细胞形状来影响表型,评估了体外调节肺泡上皮细胞(AEC)表型对T1alpha表达的影响。为了研究可溶性因子对T1alpha表达的影响,将大鼠AT2细胞在无血清培养基(MDSF)或补充牛血清(BS,10%),大鼠血清(RS,5%)的MDSF中的聚碳酸酯滤膜上生长)或培养中第0天或第4天到第8天的角质形成细胞生长因子(KGF,10 ng / ml)。为了研究细胞形状对T1alpha表达的影响,将AT2细胞铺板在补充BS的MDSF中厚胶原蛋白凝胶上。在第1天(DG1)或第4天(DG4)分离凝胶,或将其附着直到第8天。在培养的第1天和第8天之间的间隔中收获RNA和蛋白质,并通过Northern和Western印迹法定量T1alpha表达,分别。在培养的第1天至第8天之间,在MDSF +/- BS中生长的AEC中T1alpha的表达逐渐增加,这与向AT1细胞表型的过渡一致。从第0天开始接触RS或KGF可以防止第8天T1alpha表达的增加,而从第4天到第8天添加任一因子都可以逆转这种增加。在附着的凝胶上培养的AEC在第4天和第8天表达高水平的T1alpha。在DG1和DG4培养物中,T1alpha的表达均被显着抑制,这与抑制和向AT1细胞表型转变的逆转一致。这些结果表明可溶性因子和细胞形状的改变均与AEC表型平行调节T1alpha表达,并为AT2和AT1细胞表型之间的转分化至少部分可逆的概念提供了进一步的支持。

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