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神经激肽-1受体再敏化先于受体再循环。

Neurokinin-1 receptor resensitization precedes receptor recycling.

作者信息

Bennett V J, Perrine S A, Simmons M A

机构信息

Department of Physiology and Pharnacy, Northwesterm Ohio Universities College of Medicine, Rootstown, 44272, USA.

出版信息

J Pharmacol Exp Ther. 2005 Jun;313(3):1347-54. doi: 10.1124/jpet.104.079954. Epub 2005 Mar 11.

Abstract

Following agonist binding, neurokinin-1 receptors undergo rapid desensitization followed by internalization and recycling. Desensitization requires receptor phosphorylation but does not require internalization, whereas resensitization is thought to require internalization and recycling. Our previous data, however, have suggested that, following activation and desensitization, the return of responsiveness to the neurokinin-1 agonist substance P (termed "resensitization") occurs hours before internalized receptors are recycled back to the plasma membrane. To further investigate this novel mechanism of neurokinin-1 receptor resensitization, we have studied the time courses of neurokinin-1 receptor responsiveness, recycling, and dephosphorylation by measuring cellular Ca(2+) responses, ligand-receptor binding, and receptor phosphorylation, respectively. Concentration-response curves and competition binding curves were obtained at various times following desensitization. The effects of the nonhydrolyzable GTP analog Gpp(NH)p on substance P binding were also studied to assess receptor-G protein coupling. After receptor activation and desensitization, Ca(2+) signaling in response to substance P occurred within 90 min, whereas the return of receptor binding required 240 min. Receptor dephosphorylation was greater than 90% complete 20 min after agonist washout. In addition, the return of substance P responsiveness coincided with a return in sensitivity of substance P binding to Gpp(NH)p, indicating a return in receptor-G protein coupling. These data show that the resensitization of responsiveness to substance P precedes receptor recycling. This may result from a conversion of nonfunctional neurokinin-1 receptors to functional receptors at the plasma membrane.

摘要

激动剂结合后,神经激肽-1受体迅速脱敏,随后发生内化和再循环。脱敏需要受体磷酸化,但不需要内化,而重新敏化被认为需要内化和再循环。然而,我们之前的数据表明,在激活和脱敏后,对神经激肽-1激动剂P物质的反应性恢复(称为“重新敏化”)在内化受体再循环回到质膜前数小时就已发生。为了进一步研究神经激肽-1受体重新敏化的这一新机制,我们分别通过测量细胞Ca(2+)反应、配体-受体结合和受体磷酸化,研究了神经激肽-1受体反应性、再循环和去磷酸化的时间进程。在脱敏后的不同时间获得浓度-反应曲线和竞争结合曲线。还研究了不可水解的GTP类似物Gpp(NH)p对P物质结合的影响,以评估受体-G蛋白偶联。受体激活和脱敏后,对P物质的Ca(2+)信号在90分钟内出现,而受体结合的恢复需要240分钟。激动剂洗脱20分钟后,受体去磷酸化完成超过90%。此外,P物质反应性的恢复与P物质与Gpp(NH)p结合敏感性的恢复一致,表明受体-G蛋白偶联恢复。这些数据表明,对P物质反应性的重新敏化先于受体再循环。这可能是由于质膜上无功能的神经激肽-1受体转变为有功能的受体所致。

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