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表皮生长因子、血清和核苷酸诱导单个A431细胞胞质游离钙增加的研究。

Studies on the increase in cytosolic free calcium induced by epidermal growth factor, serum, and nucleotides in individual A431 cells.

作者信息

Gonzalez F A, Gross D J, Heppel L A, Webb W W

机构信息

Section of Biochemistry, Molecular and Cell Biology, Cornell University, Ithaca, New York 14853.

出版信息

J Cell Physiol. 1988 May;135(2):269-76. doi: 10.1002/jcp.1041350214.

Abstract

The response of cytosolic calcium [Ca2+]i to epidermal growth factor (EGF), fetal calf serum, and nucleotides was determined in individual A431 cells, using the fluorescent probe fura-2 and quantitative digital video fluorescence microscopy. In the presence of 1 mM external Ca2+, EGF caused a rapid rise in [Ca2+]i, followed by a slower and variable decrease. The cells responded after a lag that varied from 10 to 30 seconds, and there was considerable cell-to-cell variation in extent of the rise in [Ca2+]i. A second challenge with EGF gave negative results. No response was obtained in nominally Ca2+-free medium supplemented with 100 microM EGTA. Somewhat similar results were obtained with fetal calf serum except that a rise in [Ca2+]i was observed both in the presence and absence of external Ca2+. The A431 cells responded to external ATP with a rise in [Ca2+]i in less than 10 seconds, both in Ca2+-containing and Ca2+-free media. A coverslip with attached cells was mounted on a small chamber, allowing complete change of medium in 2 seconds. A nearly full response was obtained with only 10 seconds of contact of cells with ATP-containing medium. After washing out ATP, there was little or no response to a second addition given 100 seconds after the first. However, a second response was obtained when the concentration of agonist was increased 10-20-fold. These data favor the idea of receptor desensitization. Both homologous and heterologous receptor desensitization was observed. A transient rise in [Ca2+]i was also noted with UTP, while ITP and CTP were inactive.

摘要

利用荧光探针fura - 2和定量数字视频荧光显微镜,在单个A431细胞中测定了胞质钙[Ca2+]i对表皮生长因子(EGF)、胎牛血清和核苷酸的反应。在存在1 mM细胞外Ca2+的情况下,EGF导致[Ca2+]i迅速升高,随后是较慢且变化不定的下降。细胞在10至30秒不等的延迟后作出反应,并且[Ca2+]i升高的程度在细胞间存在相当大的差异。用EGF再次刺激得到阴性结果。在添加100 microM EGTA的名义上无Ca2+的培养基中未获得反应。用胎牛血清得到了 somewhat 相似的结果,只是在存在和不存在细胞外Ca2+的情况下均观察到[Ca2+]i升高。A431细胞在含Ca2+和无Ca2+的培养基中对细胞外ATP的反应均是在不到10秒内[Ca2+]i升高。将带有附着细胞的盖玻片安装在一个小室上,可在2秒内完全更换培养基。细胞与含ATP的培养基仅接触10秒就获得了几乎完全的反应。洗去ATP后,在第一次添加100秒后再次添加时几乎没有反应。然而,当激动剂浓度增加10 - 20倍时获得了第二次反应。这些数据支持受体脱敏的观点。观察到了同源和异源受体脱敏。UTP也引起[Ca2+]i短暂升高,而ITP和CTP无活性。 (注:原文中“Somewhat”翻译为“ somewhat”可能有误,推测应为“Somewhat”,意为“有点,稍微” ,这里按正确理解翻译为“有点” )

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