Amsler K
Department of Physiology and Biophysics, UMDNJ-Robert Wood Johnson Medical School, Piscataway 08854.
J Cell Physiol. 1994 May;159(2):331-9. doi: 10.1002/jcp.1041590216.
Populations of the renal epithelial cell line, LLC-PK1, acquire many properties characteristic of the proximal tubular cell at confluence. At confluence cells both enter a nonproliferative state and develop extensive cell-cell contacts. To determine if one or both factors is responsible for acquisition of the differentiated phenotype, growth arrest was initiated in populations of varying densities by two procedures (serum deprivation and thymidine block) and expression of several differentiated properties (Na-hexose symport activity, gamma-glutamyl transpeptidase activity, alkaline phosphatase activity, and villin protein) was examined. Induction of growth arrest resulted in expression of all differentiated properties even in subconfluent populations. The level of expression in a population was proportional to cell density at the initiation of growth arrest; higher density was associated with increased expression. Evidence indicated the existence of some minimal density below which cells could not express detectable levels of differentiated properties in response to induction of growth arrest. The procedure used to initiate growth arrest did not affect this behavior, indicating that initiation of cell growth arrest rather than hormone deprivation was the inducing factor. These results indicate that both cell growth state and cell density independently modulate expression of differentiated properties by the LLC-PK1 cell. These results are incorporated into a model in which cells in the absence of "appropriate" cell-cell contact arrest at a differentiation-incompetent cell cycle point. In the presence of appropriate cell-cell contact (as yet undefined) cells arrest at a distinct differentiation-competent cell cycle point and initiate expression of the differentiated phenotype.
肾上皮细胞系LLC-PK1在汇合时会获得许多近端肾小管细胞的特征性特性。汇合时,细胞既进入非增殖状态,又形成广泛的细胞间接触。为了确定是其中一个还是两个因素导致了分化表型的获得,通过两种方法(血清剥夺和胸腺嘧啶核苷阻断)在不同密度的细胞群体中引发生长停滞,并检测几种分化特性(钠-己糖共转运活性、γ-谷氨酰转肽酶活性、碱性磷酸酶活性和绒毛蛋白)的表达。生长停滞的诱导导致即使在亚汇合群体中所有分化特性也得以表达。一个群体中的表达水平与生长停滞开始时的细胞密度成正比;较高的密度与增加的表达相关。有证据表明存在某种最低密度,低于该密度时细胞在生长停滞诱导下无法表达可检测水平的分化特性。用于引发生长停滞的方法不影响这种行为,表明细胞生长停滞的引发而非激素剥夺是诱导因素。这些结果表明细胞生长状态和细胞密度均可独立调节LLC-PK1细胞分化特性的表达。这些结果被纳入一个模型,其中在没有“适当”细胞间接触的情况下,细胞在一个无分化能力的细胞周期点停滞。在存在适当细胞间接触(尚未明确)的情况下,细胞在一个不同的有分化能力的细胞周期点停滞,并开始表达分化表型。