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Transient Receptor potential Vanilloid (TRPV) channels are a group of cation channels that are expressed in a wide variety of tissues and are involved in regulating several cellular processes. An alteration in their expression and cellular localization is associated with various pathologies. In this study, we investigated the expression and localization of TRPV1-4 channels in human and rat corneas. TRPV 1-4 channels were found to be expressed in the epithelium, keratocytes, and endothelium of both species, which was confirmed at the gene and protein levels through PCR analysis and immunostaining. The channels were seen to be largely distributed at the cell membrane and cytoplasm, but the intensity of staining, quantified using Image J software, varied within and between cell layers. In addition, we found nuclear expression of these channels in corneal cells, and the same was quantified using ImageJ software. In both species, robust expression of TRPV1-4 channels, including in the cell nuclei, was noted in the epithelium and endothelium, compared to the stromal cells. This study provides evidence for the expression of TRPV2 and 3 channels, for which there is limited information in the corneal cells. In conclusion, this study confirms the expression of TRPV1-4 channels in the corneal cells of both species.
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http://dx.doi.org/10.1016/j.exer.2025.110616 | DOI Listing |
Exp Eye Res
August 2025
Prof. Brien Holden Eye Research Centre, LV Prasad Eye Institute, Hyderabad, Telangana, 500034, India. Electronic address:
Transient Receptor potential Vanilloid (TRPV) channels are a group of cation channels that are expressed in a wide variety of tissues and are involved in regulating several cellular processes. An alteration in their expression and cellular localization is associated with various pathologies. In this study, we investigated the expression and localization of TRPV1-4 channels in human and rat corneas.
View Article and Find Full Text PDFBiomed Pharmacother
August 2025
Channelopathy Research Center (CRC), Dongguk University College of Medicine, 32 Dongguk-ro, Ilsan Dong-gu, Goyang, Gyeonggi-do 10326, South Korea; Department of Internal Medicine, Graduate School of Medicine, Dongguk University, 27 Dongguk-ro, Ilsan Dong-gu, Goyang, Gyeonggi-do 10326, South Korea. E
Background: Allergic rhinitis (AR) affects approximately 400 million people globally and causes rhinorrhea, nasal congestion, and sneezing. Nonetheless, current treatments often provide incomplete relief and have side effects. Recent studies have indicated that various ion channels contribute to AR symptoms, suggesting that multichannel targeting may offer a more effective treatment.
View Article and Find Full Text PDFAutoimmun Rev
July 2025
Department of Dermatology, The Second Xiangya Hospital of Central South University; Hunan Key Laboratory of Medical Epigenomics, 139 Middle Renmin Road, Changsha, Hunan 410011, China; Furong Laboratory, 88 Xiangya Road, Kaifu District, Changsha, Hunan, China. Electronic address:
The transient receptor potential vanilloid (TRPV) is a family of tetrameric cation channels, expressed in various tissues and cell types. It includes thermosensitive isoforms (TRPV1-4) and calcium-permeable members (TRPV5-6). In the context of autoimmune diseases, TRPV channels have been firmly established as pivotal regulators that bridge changes in the cellular environment to the immune system.
View Article and Find Full Text PDFNeuropharmacology
November 2025
School of Biological Sciences, National Institute of Science Education and Research (NISER), Bhubaneswar, India; Homi Bhabha National Institute (HBNI), Mumbai, India. Electronic address:
Thermosensitive TRPV1-4-channels have emerged as novel regulators of neuronal function and behaviour. In midbrain, while TRPV1/TRPV3 regulates ventral tegmental area dopamine (DA) (VTA) neurons, TRPV1/TRPV3/TRPV4 play a role in the modulation of substantia nigra DA (SN) neurons. Although TRPV2 is widely expressed in the brain, its significance in the regulation of VTA/SN neurons is unclear.
View Article and Find Full Text PDFCommun Biol
May 2025
Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, USA.
ThermoTRPV1-4 channels are involved in the regulation of multiple physiological processes, including thermo- and pain perception, thermoregulation, itch, and nociception and therefore tight control of their activity is a critical requirement for correct perception of noxious stimuli and pain. We previously reported a voltage-dependent inhibition of TRPV1-4 channels by intracellular polyamines that could be explained by high affinity spermine binding in, and passage through, the permeation path. Here, using electrophysiology and cryo-electron microscopy, we elucidate molecular details of TRPV3 blockade by endogenous spermine and its analog NASPM.
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