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TRPM1 在人视网膜中的超微结构定位和表达。

Ultrastructural localization and expression of TRPM1 in the human retina.

机构信息

Departments of Retinal Signal Processing, Amsterdam, The Netherlands.

出版信息

Invest Ophthalmol Vis Sci. 2011 Oct 21;52(11):8356-62. doi: 10.1167/iovs.11-7575.

Abstract

PURPOSE

Transient receptor potential subfamily melastatin (TRPM)1 cation channels of retinal ON-bipolar cells are modulated via a mGluR6 (GMR6) signaling cascade. While light-microscopy shows these channels are located on the tips of ON-bipolar cells dendrites, near rod and cone synaptic ribbons, TRPM1 localization at the electron-microscope level is currently not described. The authors report here the ultrastructural localization of TRPM1 in the human retina.

METHODS

TRPM1 was localized in postmortem human retinas by immunohistochemistry at both the light and electron microscope levels. Additionally, TRPM1 expression was studied using in situ hybridization, laser dissection microscopy, and PCR techniques.

RESULTS

TRPM1-immunoreactivity was located on the dendrites and soma of ON-bipolar cells at the light microscope level. At the electron microscope level TRPM1-immunoreactivity was located on the tips of ON-bipolar cell dendrites that were invaginating cone pedicles and rod spherules. In addition, TRPM1-immunoreactivity was occasionally found on the rod spherules ribbons, suggesting that at least a proportion of rods may also express TRPM1. In situ hybridization showed TRPM1 encoding RNA in inner nuclear layer somata and in some photoreceptors. The presence of TRPM1-RNA in photoreceptors was confirmed by PCR in pure photoreceptor material obtained with a laser dissection microscope.

CONCLUSIONS

In the human retina TRPM1 is expressed on ON-bipolar cell dendrites that invaginate photoreceptor terminals. TRPM1 is also expressed on the synaptic ribbons of a subclass of rods, suggesting a dual function for TRPM1 in the ON-pathway.

摘要

目的

视网膜 ON-双极细胞瞬时受体电位亚家族 melastatin (TRPM)1 阳离子通道通过 mGluR6 (GMR6) 信号级联进行调节。虽然光镜显示这些通道位于 ON-双极细胞树突的末端,靠近杆和锥突触带附近,但 TRPM1 在电子显微镜水平的定位目前尚未描述。作者在此报告 TRPM1 在人视网膜中的超微结构定位。

方法

通过免疫组织化学在光镜和电子显微镜水平上定位死后人类视网膜中的 TRPM1。此外,还使用原位杂交、激光切割显微镜和 PCR 技术研究 TRPM1 的表达。

结果

TRPM1 免疫反应性位于 ON-双极细胞树突和体的光镜水平。在电子显微镜水平上,TRPM1 免疫反应性位于向内凹陷的锥突和杆小体的 ON-双极细胞树突的末端。此外,TRPM1 免疫反应性偶尔出现在杆小体带条上,表明至少一部分杆也可能表达 TRPM1。原位杂交显示 TRPM1 编码 RNA 在核内层体和一些光感受器中。通过激光切割显微镜获得的纯光感受器材料的 PCR 证实了光感受器中存在 TRPM1-RNA。

结论

在人视网膜中,TRPM1 表达在向内凹陷的光感受器末端的 ON-双极细胞树突上。TRPM1 也表达在杆的亚类的突触带上,表明 TRPM1 在 ON 途径中具有双重功能。

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