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上皮细胞收缩中的钙

Calcium in epithelial cell contraction.

作者信息

Lee H C, Auersperg N

出版信息

J Cell Biol. 1980 May;85(2):325-36. doi: 10.1083/jcb.85.2.325.

Abstract

Epithelial morphogenesis in many organs involves asymmetric microfilament-mediated cellular contractions. Similar contractions, in terms of ultrastructure and cytochalasin B sensitivity, can be induced in the carcinoma cell line C-4II in culture. This line was used to compare total intracellular calcium levels ([Ca]i) in contracted monolayer fragments and in control cultures, and to determine whether epithelial cell contraction depends on influx of extracellular Ca. [Ca]i, defined as Ca not displaceable by lanthanum, was measured by atomic absorption spectrophotometry. Degrees of contraction were determined from shape changes of monolayer fragments. Detachment from the growth surface initiated cellular contractions and caused an immediate increase in [Ca]i, from 1.0 to 4.0-5.0 micrograms Ca/mg protein in early confluent cultures, and from 0.3 to 1.0-2.0 micrograms Ca/mg protein in crowded cultures. This increase was followed by a gradual decline in [Ca]i, though Ca levels remained higher than in controls and contraction progressed for 30 min. Contraction was inhibited completely by cold (7 degrees C) and by Ca-free medium, and in a dose-dependent manner by papaverine (2.5 x 10(-6) M-2.5 x 10(-4) M), lanthanum (1.0 x 10(-6) M-1.0 x 10(-4) M); and D-600 (1.0-2.0 x 10(-4) M). The Ca ionophore A23187 had no effect at 5.0 x 10(-6) M and was inhibitory at higher concentrations. The results provided direct evidence for increased [Ca]i in contracting epithelial cells, and suggest that Ca influx is required for such contraction to take place.

摘要

许多器官中的上皮形态发生涉及不对称微丝介导的细胞收缩。在超微结构和细胞松弛素B敏感性方面,类似的收缩可在培养的癌细胞系C - 4II中诱导产生。该细胞系用于比较收缩的单层片段和对照培养物中的细胞内总钙水平([Ca]i),并确定上皮细胞收缩是否依赖于细胞外钙的流入。[Ca]i定义为不能被镧取代的钙,通过原子吸收分光光度法测量。收缩程度由单层片段的形状变化确定。从生长表面脱离引发细胞收缩,并导致[Ca]i立即增加,在早期汇合培养物中从1.0微克钙/毫克蛋白质增加到4.0 - 5.0微克钙/毫克蛋白质,在拥挤培养物中从0.3微克钙/毫克蛋白质增加到1.0 - 2.0微克钙/毫克蛋白质。这种增加之后是[Ca]i逐渐下降,尽管钙水平仍高于对照,并且收缩持续30分钟。收缩完全被低温(7℃)和无钙培养基抑制,并被罂粟碱(2.5×10^(-6)M - 2.5×10^(-4)M)、镧(1.0×10^(-6)M - 1.0×10^(-4)M)和D - 600(1.0 - 2.0×10^(-4)M)以剂量依赖方式抑制。钙离子载体A23187在5.0×10^(-6)M时无作用,在更高浓度时具有抑制作用。结果为收缩的上皮细胞中[Ca]i增加提供了直接证据,并表明这种收缩需要钙流入。

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