Department of Anesthesiology, Duke University Medical Center, Durham, NC 27710, USA.
Cell Rep. 2012 Jan 26;1(1):43-55. doi: 10.1016/j.celrep.2011.11.002.
Specialized somatosensory neurons detect temperatures ranging from pleasantly cool or warm to burning hot and painful (nociceptive). The precise temperature ranges sensed by thermally sensitive neurons is determined by tissue-specific expression of ion channels of the transient receptor potential(TRP) family.We show here that in Drosophila, TRPA1 is required for the sensing of nociceptive heat. We identify two previously unidentified protein isoforms of dTRPA1, named dTRPA1-C and dTRPA1-D, that explain this requirement. A dTRPA1-C/D reporter was exclusively expressed in nociceptors, and dTRPA1-C rescued thermal nociception phenotypes when restored to mutant nociceptors. However,surprisingly, we find that dTRPA1-C is not a direct heat sensor. Alternative splicing generates at least four isoforms of dTRPA1. Our analysis of these isoforms reveals a 37-amino-acid-long intracellular region (encoded by a single exon) that is critical for dTRPA1 temperature responses. The identification of these amino acids opens the door to a biophysical understanding of a molecular thermosensor.
专门的躯体感觉神经元可以检测到从宜人的凉爽或温暖到灼热和疼痛(伤害性)的温度范围。热敏神经元感知的精确温度范围由瞬时受体电位(TRP)家族的离子通道的组织特异性表达决定。在这里,我们表明在果蝇中,TRPA1 是伤害性热感觉所必需的。我们鉴定了两种以前未识别的 dTRPA1 蛋白异构体,分别命名为 dTRPA1-C 和 dTRPA1-D,它们解释了这种需求。dTRPA1-C/D 报告基因仅在伤害感受器中表达,并且当恢复到突变型伤害感受器时,dTRPA1-C 挽救了热伤害感受表型。然而,令人惊讶的是,我们发现 dTRPA1-C 不是直接的热传感器。选择性剪接产生至少四种 dTRPA1 异构体。我们对这些异构体的分析揭示了一个 37 个氨基酸长的细胞内区域(由单个外显子编码),对于 dTRPA1 的温度反应至关重要。这些氨基酸的鉴定为理解分子热敏传感器的生物物理学特性打开了大门。