Deering-Rice Cassandra E, Stockmann Chris, Romero Erin G, Lu Zhenyu, Shapiro Darien, Stone Bryan L, Fassl Bernhard, Nkoy Flory, Uchida Derek A, Ward Robert M, Veranth John M, Reilly Christopher A
From the Department of Pharmacology and Toxicology, University of Utah, Salt Lake City, Utah 84112 and.
Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah 84108.
J Biol Chem. 2016 Nov 25;291(48):24866-24879. doi: 10.1074/jbc.M116.746156. Epub 2016 Oct 7.
Transient receptor potential (TRP) channels are activated by environmental particulate materials. We hypothesized that polymorphic variants of transient receptor potential vanilloid-1 (TRPV1) would be uniquely responsive to insoluble coal fly ash compared with the prototypical soluble agonist capsaicin. Furthermore, these changes would manifest as differences in lung cell responses to these agonists and perhaps correlate with changes in asthma symptom control. The TRPV1-I315M and -T469I variants were more responsive to capsaicin and coal fly ash. The I585V variant was less responsive to coal fly ash particles due to reduced translation of protein and an apparent role for Ile-585 in activation by particles. In HEK-293 cells, I585V had an inhibitory effect on wild-type TRPV1 expression, activation, and internalization/agonist-induced desensitization. In normal human bronchial epithelial cells, IL-8 secretion in response to coal fly ash treatment was reduced for cells heterozygous for TRPV1-I585V. Finally, both the I315M and I585V variants were associated with worse asthma symptom control with the effects of I315M manifesting in mild asthma and those of the I585V variant manifesting in severe, steroid-insensitive individuals. This effect may be due in part to increased transient receptor potential ankyrin-1 (TRPA1) expression by lung epithelial cells expressing the TRPV1-I585V variant. These findings suggest that specific molecular interactions control TRPV1 activation by particles, differential activation, and desensitization of TRPV1 by particles and/or other agonists, and cellular changes in the expression of TRPA1 as a result of I585V expression could contribute to variations in asthma symptom control.
瞬时受体电位(TRP)通道可被环境颗粒物激活。我们推测,与典型的可溶性激动剂辣椒素相比,瞬时受体电位香草酸受体1(TRPV1)的多态性变体对不溶性煤飞灰具有独特的反应性。此外,这些变化将表现为肺细胞对这些激动剂反应的差异,并且可能与哮喘症状控制的变化相关。TRPV1 - I315M和 - T469I变体对辣椒素和煤飞灰更敏感。I585V变体对煤飞灰颗粒的反应性较低,这是由于蛋白质翻译减少以及异亮氨酸 - 585在颗粒激活中具有明显作用。在人胚肾293(HEK - 293)细胞中,I585V对野生型TRPV1的表达、激活以及内化/激动剂诱导的脱敏具有抑制作用。在正常人支气管上皮细胞中,TRPV1 - I585V杂合细胞对煤飞灰处理的白细胞介素 - 8分泌减少。最后,I315M和I585V变体均与较差的哮喘症状控制相关,I315M的影响在轻度哮喘中表现,而I585V变体的影响在重度、激素不敏感个体中表现。这种效应可能部分归因于表达TRPV1 - I585V变体的肺上皮细胞中瞬时受体电位锚蛋白1(TRPA1)表达增加。这些发现表明,特定的分子相互作用控制颗粒对TRPV1的激活、颗粒和/或其他激动剂对TRPV1的差异激活和脱敏,以及由于I585V表达导致的TRPA1表达的细胞变化可能导致哮喘症状控制方面的差异。