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甲状腺胺可诱导人结膜上皮细胞中的瞬时受体电位阳离子通道亚家族M成员8(TRPM8)通道激活。

Thyronamine induces TRPM8 channel activation in human conjunctival epithelial cells.

作者信息

Khajavi Noushafarin, Reinach Peter S, Slavi Nefeli, Skrzypski Marek, Lucius Alexander, Strauß Olaf, Köhrle Josef, Mergler Stefan

机构信息

Charité-Universitätsmedizin Berlin, Campus Virchow-Klinikum, Klinik für Augenheilkunde, Augustenburger Platz 1, D-13353 Berlin, Germany.

Biological Sciences, SUNY College of Optometry, New York, NY 10036, USA; School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou 325027, PR China.

出版信息

Cell Signal. 2015 Feb;27(2):315-25. doi: 10.1016/j.cellsig.2014.11.015. Epub 2014 Nov 21.

Abstract

3-Iodothyronamine (T1AM), an endogenous thyroid hormone (TH) metabolite, induces numerous responses including a spontaneously reversible body temperature decline. As such an effect is associated in the eye with increases in basal tear flow and thermosensitive transient receptor potential melastatin 8 (TRPM8) channel activation, we determined in human conjunctival epithelial cells (IOBA-NHC) if T1AM also acts as a cooling agent to directly affect TRPM8 activation at a constant temperature. RT-PCR and quantitative real-time PCR (qPCR) along with immunocytochemistry probed for TRPM8 gene and protein expression whereas functional activity was evaluated by comparing the effects of T1AM with those of TRPM8 mediators on intracellular Ca(2+) ([Ca(2+)]i) and whole-cell currents. TRPM8 gene and protein expression was evident and icilin (20μM), a TRPM8 agonist, increased Ca(2+) influx as well as whole-cell currents whereas BCTC (10μM), a TRPM8 antagonist, suppressed these effects. Similarly, either temperature lowering below 23°C or T1AM (1μM) induced Ca(2+) transients that were blocked by this antagonist. TRPM8 activation by both 1µM T1AM and 20μM icilin prevented capsaicin (CAP) (20μM) from inducing increases in Ca(2+) influx through TRP vanilloid 1 (TRPV1) activation, whereas BCTC did not block this response. CAP (20μM) induced a 2.5-fold increase in IL-6 release whereas during exposure to 20μM capsazepine this rise was completely blocked. Similarly, T1AM (1μM) prevented this response. Taken together, T1AM like icilin is a cooling agent since they both directly elicit TRPM8 activation at a constant temperature. Moreover, there is an inverse association between changes in TRPM8 and TRPV1 activity since these cooling agents blocked both CAP-induced TRPV1 activation and downstream rises in IL-6 release.

摘要

3-碘甲腺原氨酸(T1AM)是一种内源性甲状腺激素(TH)代谢产物,可引发多种反应,包括体温自发且可逆地下降。鉴于这种效应在眼部与基础泪液分泌增加以及热敏性瞬时受体电位香草酸亚型8(TRPM8)通道激活有关,我们在人结膜上皮细胞(IOBA-NHC)中研究了T1AM是否也作为一种冷却剂,在恒定温度下直接影响TRPM8的激活。采用逆转录聚合酶链反应(RT-PCR)和定量实时聚合酶链反应(qPCR)以及免疫细胞化学方法检测TRPM8基因和蛋白表达,而通过比较T1AM与TRPM8介质对细胞内钙离子([Ca(2+)]i)和全细胞电流的影响来评估功能活性。TRPM8基因和蛋白表达明显,TRPM8激动剂艾西利定(20μM)可增加Ca(2+)内流以及全细胞电流,而TRPM8拮抗剂2-[[2-[[3-氯-5-(三氟甲基)苯基]甲基]硫代]乙基]异吲哚-1,3-二酮(BCTC,10μM)可抑制这些效应。同样,温度降至23°C以下或T1AM(1μM)均可诱导Ca(2+)瞬变,且这种瞬变可被该拮抗剂阻断。1µM T1AM和20μM艾西利定激活TRPM8均可阻止辣椒素(CAP,20μM)通过瞬时受体电位香草酸亚型1(TRPV1)激活诱导Ca(2+)内流增加,而BCTC并未阻断此反应。CAP(20μM)可使白细胞介素-6(IL-6)释放增加2.5倍,而在暴露于20μM辣椒平期间,这种升高被完全阻断。同样,T1AM(1μM)也可阻止此反应。综上所述,T1AM与艾西利定一样是一种冷却剂,因为它们都能在恒定温度下直接引发TRPM8激活。此外,TRPM8和TRPV1活性变化之间存在负相关,因为这些冷却剂可阻断CAP诱导的TRPV1激活以及下游IL-6释放增加。

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