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活体视网膜细胞死亡的可视化:使用钙蛋白酶活性检测作为视网膜变性的生物标志物。

Visualizing Cell Death in Live Retina: Using Calpain Activity Detection as a Biomarker for Retinal Degeneration.

机构信息

Cell Death Mechanisms Group, Institute for Ophthalmic Research, Eberhard-Karls-Universität Tübingen, 72076 Tübingen, Germany.

Graduate Training Center of Neuroscience, Eberhard-Karls-Universität Tübingen, 72076 Tübingen, Germany.

出版信息

Int J Mol Sci. 2022 Mar 31;23(7):3892. doi: 10.3390/ijms23073892.

Abstract

Calpains are a family of calcium-activated proteases involved in numerous disorders. Notably, previous studies have shown that calpain activity was substantially increased in various models for inherited retinal degeneration (RD). In the present study, we tested the capacity of the calpain-specific substrate -BOC-Leu-Met-CMAC to detect calpain activity in living retina, in organotypic retinal explant cultures derived from wild-type mice, as well as from and RD-mutant mice. Test conditions were refined until the calpain substrate readily detected large numbers of cells in the photoreceptor layer of RD retina but not in wild-type retina. At the same time, the calpain substrate was not obviously toxic to photoreceptor cells. Comparison of calpain activity with immunostaining for activated calpain-2 furthermore suggested that individual calpain isoforms may be active in distinct temporal stages of photoreceptor cell death. Notably, calpain-2 activity may be a relatively short-lived event, occurring only towards the end of the cell-death process. Finally, our results support the development of calpain activity detection as a novel in vivo biomarker for RD suitable for combination with non-invasive imaging techniques.

摘要

钙蛋白酶是一类钙激活的蛋白酶,参与多种疾病。值得注意的是,先前的研究表明,钙蛋白酶活性在各种遗传性视网膜变性 (RD) 的模型中显著增加。在本研究中,我们测试了钙蛋白酶特异性底物 -BOC-Leu-Met-CMAC 在活体视网膜、源自野生型小鼠的器官型视网膜外植体培养物以及 和 RD 突变型小鼠中检测钙蛋白酶活性的能力。我们对测试条件进行了优化,直到钙蛋白酶底物能够轻易地检测到 RD 视网膜感光细胞层中的大量细胞,但在野生型视网膜中则不能。同时,钙蛋白酶底物对感光细胞没有明显的毒性。钙蛋白酶活性与激活型钙蛋白酶-2 的免疫染色比较进一步表明,不同的钙蛋白酶同工酶可能在感光细胞死亡的不同时间阶段发挥作用。值得注意的是,钙蛋白酶-2 活性可能是一个相对短暂的事件,仅发生在细胞死亡过程的末期。最后,我们的结果支持将钙蛋白酶活性检测作为一种新的适合与非侵入性成像技术相结合的 RD 体内生物标志物的发展。

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