Kirstein Emilie, Schaudien Dirk, Wagner Mathias, Diebolt Coline M, Bozzato Alessandro, Tschernig Thomas, Englisch Colya N
Institute for Anatomy and Cell Biology, Saarland University, 66421 Homburg, Germany.
Fraunhofer Institute for Toxicology and Experimental Medicine, 30625 Hanover, Germany.
Int J Mol Sci. 2024 Apr 16;25(8):4392. doi: 10.3390/ijms25084392.
Transient receptor potential canonical sub-family channel 3 (TRPC3) is considered to play a critical role in calcium homeostasis. However, there are no established findings in this respect with regard to TRPC6. Although the parathyroid gland is a crucial organ in calcium household regulation, little is known about the protein distribution of TRPC channels-especially TRPC3 and TRPC6-in this organ. Our aim was therefore to investigate the protein expression profile of TRPC3 and TRPC6 in healthy and diseased human parathyroid glands. Surgery samples from patients with healthy parathyroid glands and from patients suffering from primary hyperparathyroidism (pHPT) were investigated by immunohistochemistry using knockout-validated antibodies against TRPC3 and TRPC6. A software-based analysis similar to an H-score was performed. For the first time, to our knowledge, TRPC3 and TRPC6 protein expression is described here in the parathyroid glands. It is found in both chief and oxyphilic cells. Furthermore, the TRPC3 staining score in diseased tissue (pHPT) was statistically significantly lower than that in healthy tissue. In conclusion, TRPC3 and TRPC6 proteins are expressed in the human parathyroid gland. Furthermore, there is strong evidence indicating that TRPC3 plays a role in pHPT and subsequently in parathyroid hormone secretion regulation. These findings ultimately require further research in order to not only confirm our results but also to further investigate the relevance of these channels and, in particular, that of TRPC3 in the aforementioned physiological functions and pathophysiological conditions.
瞬时受体电位香草酸亚家族通道3(TRPC3)被认为在钙稳态中起关键作用。然而,关于TRPC6在这方面尚无既定的研究结果。尽管甲状旁腺是钙稳态调节中的关键器官,但对于TRPC通道(尤其是TRPC3和TRPC6)在该器官中的蛋白质分布知之甚少。因此,我们的目的是研究健康和患病人类甲状旁腺中TRPC3和TRPC6的蛋白质表达谱。使用针对TRPC3和TRPC6的经敲除验证的抗体,通过免疫组织化学对来自健康甲状旁腺患者和原发性甲状旁腺功能亢进症(pHPT)患者的手术样本进行了研究。进行了类似于H评分的基于软件的分析。据我们所知,首次在此描述了甲状旁腺中TRPC3和TRPC6的蛋白质表达。在主细胞和嗜酸性细胞中均发现了该表达。此外,患病组织(pHPT)中的TRPC3染色评分在统计学上显著低于健康组织中的评分。总之,TRPC3和TRPC6蛋白在人类甲状旁腺中表达。此外,有强有力的证据表明TRPC3在pHPT中起作用,并随后在甲状旁腺激素分泌调节中起作用。这些发现最终需要进一步研究,以便不仅证实我们的结果,而且进一步研究这些通道的相关性,特别是TRPC3在上述生理功能和病理生理状况中的相关性。