Baudry Michel, Su Wenyue, Seinfeld Jeffrey, Sun Jiandong, Bi Xiaoning
Graduate College of Biomedical Sciences, Western University of Health Sciences, Pomona, CA, United States.
College of Osteopathic Medicine of the Pacific, Western University of Health Sciences, Pomona, CA, United States.
Front Mol Biosci. 2021 Jun 15;8:685938. doi: 10.3389/fmolb.2021.685938. eCollection 2021.
While calpains have been implicated in neurogenesis for a long time, there is still little information regarding the specific contributions of various isoforms in this process. We took advantage of the availability of mutant mice with complete deletion of calpain-1 to analyze its contribution to neurogenesis. We first used the incorporation of BrdU in newly-generated cells in the subgranular zone of the dentate gyrus to determine the role of calpain-1 deletion in neuronal proliferation. Our results showed that the lack of calpain-1 decreased the rate of cell proliferation in adult hippocampus. As previously shown, it also decreased the long-term survival of newly-generated neurons. We also used data from previously reported RNA and miRNA sequencing analyses to identify differentially expressed genes in brain of calpain-1 knock-out mice related to cell division, cell migration, cell proliferation and cell survival. A number of differentially expressed genes were identified, which could play a significant role in the changes in neurogenesis in calpain-1 knock out mice. The results provide new information regarding the role of calpain-1 in neurogenesis and have implications for better understanding the pathologies associated with calpain-1 mutations in humans.
虽然钙蛋白酶长期以来一直被认为与神经发生有关,但关于各种同工型在这一过程中的具体作用,目前仍知之甚少。我们利用完全缺失钙蛋白酶-1的突变小鼠来分析其对神经发生的作用。我们首先通过在齿状回颗粒下区新生成细胞中掺入5-溴脱氧尿嘧啶核苷(BrdU)来确定钙蛋白酶-1缺失在神经元增殖中的作用。我们的结果表明,钙蛋白酶-1的缺失降低了成年海马体中的细胞增殖率。如先前所示,它还降低了新生成神经元的长期存活率。我们还利用先前报道的RNA和miRNA测序分析数据,来鉴定钙蛋白酶-1基因敲除小鼠大脑中与细胞分裂、细胞迁移、细胞增殖和细胞存活相关的差异表达基因。我们鉴定出了一些差异表达基因,它们可能在钙蛋白酶-1基因敲除小鼠神经发生的变化中发挥重要作用。这些结果提供了关于钙蛋白酶-1在神经发生中作用的新信息,并有助于更好地理解与人类钙蛋白酶-1突变相关的病理学。