Department of Cell Biology and Histology, Medical School, IMIB-Arrixaca, Regional Campus of International Excellence "Campus Mare Nostrum", University of Murcia, Spain.
Histol Histopathol. 2024 Oct;39(10):1295-1302. doi: 10.14670/HH-18-734. Epub 2024 Mar 13.
HSP47, a chaperone whose main function is the maturation of collagen molecules, is considered a marker of fibrotic diseases. Increased collagen synthesis in the testis has been associated with various pathologies leading to seminiferous tubule regression. Our aim was to study whether HSP47 is expressed in hamster Sertoli cells both in the adult and in two physiological situations of seminiferous tubule atrophy: irreversible testicular ageing and testicular regression due to short photoperiod (reversible). Eighteen animals were divided as follows: a group of 6 young animals aged 6 months, a group of 6 animals aged 24 months, which were exposed to a long photoperiod, and a final group of 6 young animals subjected to a short photoperiod. Testicular samples were fixed in methacarn and an immunohistochemical technique was used to detect HSP47. A semiquantitative study of of this protein expresion was performed between tubular sections of aged animals with complete spermatogenesis and arrested spermatogenesis and tubular sections with arrest spermatogenesis of photoinhibited testes. Sertoli cells were positive for HSP47, the intensity being greater in tubular sections with arrested spermatogenesis in both aged and photoinhibited animals. Semiquantitative analysis corroborated this observation in the sense that the expression of this protein differed according to the functional state of the seminiferous tubules. Thus, the radio of immunoreactivity was significantly higher in tubular sections with arrested spermatogenesis in aged animals compared with regressed animals, and in the latter compared with those whose tubular sections showed complete spermatogenesis. In conclusion, HSP47 expression in Sertoli cells was found for the first time in mammals. Moreover, increased expression seemed to be related to the degree of atrophy of the seminiferous epithelium and to the reversible or non-reversible physiological state of the seminiferous epithelium.
HSP47 是一种伴侣蛋白,主要功能是成熟胶原分子,被认为是纤维化疾病的标志物。睾丸中胶原蛋白的合成增加与导致生精小管退化的各种病变有关。我们的目的是研究 HSP47 是否在成年仓鼠支持细胞中表达,以及在两种生精小管萎缩的生理情况下表达:不可逆的睾丸老化和由于短光照周期引起的睾丸退化(可逆)。将 18 只动物分为以下三组:6 只 6 月龄的年轻动物,6 只 24 月龄的暴露于长光照周期的动物,最后一组 6 只年轻动物暴露于短光照周期。将睾丸样本固定在马卡因中,并使用免疫组织化学技术检测 HSP47。对具有完全精子发生和停止精子发生的老化动物的管状部分以及光抑制睾丸中停止精子发生的管状部分进行 HSP47 表达的半定量研究。HSP47 在支持细胞中呈阳性,在老化和光抑制动物的停止精子发生的管状部分中,其强度更大。半定量分析证实了这一观察结果,即根据生精小管的功能状态,这种蛋白质的表达不同。因此,与退化动物相比,在老化动物的停止精子发生的管状部分中,该蛋白的免疫反应率显著升高,与具有完全精子发生的管状部分相比,在后者中也显著升高。总之,在哺乳动物中首次发现 HSP47 在支持细胞中的表达。此外,表达增加似乎与生精上皮的萎缩程度以及生精上皮的可逆或不可逆生理状态有关。