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表皮生长因子刺激人类红细胞摄取钙离子。

Epidermal growth factor stimulates Ca2+ uptake of human erythrocytes.

作者信息

Engelmann B, Gross V, Schumacher U, Duhm J

机构信息

Physiologisches Institut der Universität München, Federal Republic of Germany.

出版信息

Pflugers Arch. 1992 Aug;421(5):497-502. doi: 10.1007/BF00370262.

Abstract

To examine the functional significance of epidermal growth factor (EGF) binding sites present on the human erythrocyte membrane [Engelmann et al. (1992) Am J Hematol 39:239-241], the effect of EGF on 45Ca2+ uptake and on 22Na+ efflux from these cells has been studied. In all cases media contained 1.25 mM Ca2+, whereas Na+ and K+ were varied. In 140 mM Na+/5 mM K+ medium EGF (250 ng/ml) stimulated 45Ca2+ uptake by 50%-90% in quin-2-loaded cells, and by up to threefold in untreated cells. Increasing extracellular K+ up to 75 mM at the expense of extracellular Na2+ stimulated the EGF-induced 45Ca2+ uptake by about twofold compared to 145 mM Na+ medium both in quin-2-loaded and in untreated cells. In 145 mM K+ medium, however, no EGF-induced 45Ca2+ uptake was detectable in quin-2-loaded cells, while in untreated cells Ca2+ entry was stimulated twofold by EGF. After increasing intracellular Na+ from 6 mmol/l cells to 18 mmol/l cells in untreated cells suspended in 145 mM K+ medium, 45Ca2+ uptake induced by EGF gradually increased. In contrast, in 140 mM Na+/5 mM K+ as well as in 70 mM Na+/75 mM K+ medium, 45Ca2+ uptake accelerated by EGF was largely unaffected by a modified red cell Na+ content. When 22Na-loaded untreated red cells were suspended in 145 mM K+ medium EGF stimulated red cell 22Na+ efflux by more than threefold. In 140 mM Na+/5 mM K+ as well as in 70 mM Na+/75 mM K+ medium, no 22Na+ efflux induced by the growth factor was evident.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为研究人红细胞膜上表皮生长因子(EGF)结合位点的功能意义[恩格尔曼等人(1992年),《美国血液学杂志》39:239 - 241],研究了EGF对这些细胞45Ca2+摄取和22Na+外流的影响。在所有情况下,培养基中含有1.25 mM Ca2+,而Na+和K+的浓度有所变化。在140 mM Na+/5 mM K+培养基中,EGF(250 ng/ml)使喹-2负载细胞的45Ca2+摄取增加50% - 90%,使未处理细胞的摄取增加多达三倍。以细胞外Na2+为代价将细胞外K+增加至75 mM,在喹-2负载细胞和未处理细胞中,与145 mM Na+培养基相比,EGF诱导的45Ca2+摄取增加约两倍。然而,在145 mM K+培养基中,喹-2负载细胞中未检测到EGF诱导的45Ca2+摄取,而在未处理细胞中,EGF使Ca2+内流增加两倍。在悬浮于145 mM K+培养基中的未处理细胞中,将细胞内Na+从6 mmol/l增加到18 mmol/l后,EGF诱导的45Ca2+摄取逐渐增加。相反,在140 mM Na+/5 mM K+以及70 mM Na+/75 mM K+培养基中,EGF加速的45Ca2+摄取在很大程度上不受红细胞Na+含量改变的影响。当将负载22Na的未处理红细胞悬浮于145 mM K+培养基中时,EGF使红细胞22Na+外流增加超过三倍。在140 mM Na+/5 mM K+以及70 mM Na+/75 mM K+培养基中,生长因子诱导的22Na+外流不明显。(摘要截短于250字)

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