High ambient temperature may induce presbyopia via TRPV1 activation.

IF 1.2 4区 医学 Q3 PATHOLOGY
Medical Molecular Morphology Pub Date : 2024-12-01 Epub Date: 2024-07-09 DOI:10.1007/s00795-024-00391-2
Yosuke Nakazawa, Yumika Kuno, Hibiki Shimada, Noriaki Nagai, Noriko Hiramatsu, Shun Takeda, Naoki Yamamoto, Megumi Funakoshi-Tago, Hiroshi Sasaki
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引用次数: 0

Abstract

The prevalence of presbyopia and nuclear cataracts (NUC) is reported to be higher in tropical areas than that in other regions, suggesting a potential influence of high temperatures on lens health. Transient receptor potential vanilloid (TRPV) channels play a crucial role in detecting ambient temperatures across various species, with TRPV1 and TRPV4 expressed in lens epithelial cells. In this study, we investigated whether ambient temperatures affect TRPV1 and TRPV4 activity in the lens, potentially contributing to the development of presbyopia and NUC. We conducted experiments using cultured human lens epithelial cell lines under different temperature conditions. Our results revealed that the mitogen-activated protein kinase (MEK)/extracellular signal-regulated kinase (ERK) and p38 pathways, downstream molecules of TRPV1, were activated, while Src family kinase, a downstream molecule of TRPV4, was inhibited at 37.5 °C culture compared to 35.0 °C. Confocal microscope images demonstrated higher expression of TRPV1 in 3D-structured cells under high-temperature culture conditions. Additionally, in organ culture lenses, higher elasticity was observed at elevated temperatures compared to that at lower temperatures. These results suggest that high ambient temperatures may induce lens sclerosis via TRPV1 activation, potentially contributing to the development of presbyopia and NUC.

Abstract Image

高环境温度可能会通过激活 TRPV1 引发老花眼。
据报道,热带地区的老花眼和核性白内障(NUC)发病率高于其他地区,这表明高温对晶状体健康有潜在影响。瞬时受体电位香草酸(TRPV)通道在不同物种检测环境温度的过程中发挥着至关重要的作用,TRPV1 和 TRPV4 在晶状体上皮细胞中表达。在本研究中,我们调查了环境温度是否会影响晶状体中 TRPV1 和 TRPV4 的活性,从而可能导致老花眼和 NUC 的发生。我们使用在不同温度条件下培养的人类晶状体上皮细胞系进行了实验。我们的结果表明,与 35.0 °C相比,37.5 °C培养条件下TRPV1的下游分子--丝裂原活化蛋白激酶(MEK)/细胞外信号调节激酶(ERK)和p38通路被激活,而TRPV4的下游分子--Src家族激酶则受到抑制。共聚焦显微镜图像显示,在高温培养条件下,三维结构细胞中 TRPV1 的表达量更高。此外,在器官培养透镜中,观察到高温下的弹性比低温下更高。这些结果表明,高温环境可能会通过激活 TRPV1 诱导晶状体硬化,从而可能导致老花眼和 NUC 的发生。
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来源期刊
Medical Molecular Morphology
Medical Molecular Morphology 医学-病理学
CiteScore
2.90
自引率
5.60%
发文量
30
审稿时长
>12 weeks
期刊介绍: Medical Molecular Morphology is an international forum for researchers in both basic and clinical medicine to present and discuss new research on the structural mechanisms and the processes of health and disease at the molecular level. The structures of molecules, organelles, cells, tissues, and organs determine their normal function. Disease is thus best understood in terms of structural changes in these different levels of biological organization, especially in molecules and molecular interactions as well as the cellular localization of chemical components. Medical Molecular Morphology welcomes articles on basic or clinical research in the fields of cell biology, molecular biology, and medical, veterinary, and dental sciences using techniques for structural research such as electron microscopy, confocal laser scanning microscopy, enzyme histochemistry, immunohistochemistry, radioautography, X-ray microanalysis, and in situ hybridization. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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