Mergler Stefan, Strowski Mathias Z, Kaiser Simone, Plath Thomas, Giesecke Yvonne, Neumann Marleen, Hosokawa Hiroshi, Kobayashi Shigeo, Langrehr Jan, Neuhaus Peter, Plöckinger Ursula, Wiedenmann Bertram, Grötzinger Carsten
Department of Internal Medicine, Division of Hepatology and Gastroenterology, Charité - Universitatsmedizin Berlin, Campus Virchow Klinikum, Berlin, Germany.
Neuroendocrinology. 2007;85(2):81-92. doi: 10.1159/000101693. Epub 2007 Apr 5.
TRPM8 is a member of the melastatin-type transient receptor potential ion channel family. Activation by cold or by agonists (menthol, icilin) induces a transient rise in intracellular free calcium concentration (Ca(2+)). Our previous study demonstrated that Ca(2+)-permeable cation channels play a role in IGF-1-induced secretion of chromogranin A in human neuroendocrine tumor (NET) cell line BON [Mergler et al.: Neuroendocrinology 2006;82:87-102]. Here, we extend our earlier study by investigating the expression of TRPM8 and characterizing its impact on Ca(2+) and the secretion of neurotensin (NT). We identified TRPM8 expression in NET BON cells by RT-PCR, Western blotting and immunofluorescence staining. Icilin increased Ca(2+) in TRPM8-transfected human embryonic kidney cells (HEK293) but not in mock-transfected cells. Icilin and menthol induced Ca(2+) transients in BON cells as well as in primary NET cell cultures of two different pancreatic NETs as detected by single cell fluorescence imaging. Icilin increased non-selective cation channel currents in BON cells as detected by patch-clamp recordings. This activation was associated with increased NT secretion. Taken together, this study demonstrates for the first time the expression TRPM8 in NET cells and its role in regulating Ca(2+) and NT secretion. The regulation of NT secretion in NETs by TRPM8 may have a potential clinical implication in diagnosis or therapy.
TRPM8是褪黑素型瞬时受体电位离子通道家族的成员。寒冷或激动剂(薄荷醇、异冰片)激活可诱导细胞内游离钙浓度([Ca(2+)]i)短暂升高。我们之前的研究表明,Ca(2+)可渗透阳离子通道在胰岛素样生长因子-1诱导的人神经内分泌肿瘤(NET)细胞系BON中嗜铬粒蛋白A的分泌中起作用[Mergler等人:《神经内分泌学》2006年;82:87-102]。在此,我们通过研究TRPM8的表达并表征其对[Ca(2+)]i和神经降压素(NT)分泌的影响来扩展我们早期的研究。我们通过逆转录聚合酶链反应(RT-PCR)、蛋白质免疫印迹法和免疫荧光染色在NET BON细胞中鉴定出TRPM8的表达。异冰片可增加TRPM8转染的人胚肾细胞(HEK293)中的[Ca(2+)]i,但在mock转染细胞中则不然。通过单细胞荧光成像检测发现,异冰片和薄荷醇在BON细胞以及两种不同胰腺NET的原代NET细胞培养物中诱导Ca(2+)瞬变。通过膜片钳记录检测发现,异冰片增加了BON细胞中的非选择性阳离子通道电流。这种激活与NT分泌增加有关。综上所述,本研究首次证明了TRPM8在NET细胞中的表达及其在调节[Ca(2+)]i和NT分泌中的作用。TRPM8对NET中NT分泌的调节可能在诊断或治疗方面具有潜在的临床意义。