Li Liping, Pastor Johanne, Zhang Jianning, Davidson Taylor, Hu Ming-Chang, Moe Orson W
Charles and Jane Pak Center for Mineral Metabolism and Clinical Research Dallas TX USA.
Division of Nephrology Department of Internal Medicine University of Texas Southwestern Medical Center Dallas TX USA.
FASEB Bioadv. 2021 May 19;3(7):531-540. doi: 10.1096/fba.2020-00066. eCollection 2021 Jul.
Alpha-Klotho is a multi-functional protein essential for maintenance of a myriad of cell functions. αKlotho is a single transmembrane protein with a large extracellular segment consisting of two domains (termed Kl1 and Kl2) which is shed into the extracellular fluid by proteolytic cleavage to furnish circulating soluble αKlotho. Based on cDNA sequence, an alternatively spliced mRNA is predicted to translate to a putative soluble αKlotho protein in mouse and human with only the Kl1 domain that represents a "spliced αKlotho Kl1" (spKl1) and is released from the cell without membrane targeting or cleavage. The existence of this protein remains for two decades. We generated a novel antibody (anti-spE15) against the 15 amino acid epitope (E15; VSPLTKPSVGLLLPH) which is not present in Kl1 or full-length αKlotho and validated its specific reactivity against spKl1 in vitro. Using anti-spE15 and two well-established anti-αKlotho monoclonal antibodies, we performed immunoblots, immunoprecipitation, and immunohistochemistry to investigate for expression of spKl1 in the mouse brain. We found anti-spE15 labeling in mouse brain but were not able to see co-labelling of Kl1 and spE15 epitopes on the same protein, which is the pre-requisite for the existence of a spKl1 polypeptide, indicating that anti-spE15 likely binds to another protein other than the putative spKl1. In isolated choroid plexus from mouse brain, we found strong staining with anti-spE15, but did not find the spliced αKlotho transcript. We conclude that using reliable reagents and inclusion of proper controls, there is no evidence of the spKl1 protein in the mouse brain.
α-klotho是一种多功能蛋白质,对维持众多细胞功能至关重要。α-klotho是一种单跨膜蛋白,具有一个由两个结构域(称为Kl1和Kl2)组成的大细胞外片段,该片段通过蛋白水解切割进入细胞外液,以提供循环中的可溶性α-klotho。根据cDNA序列,预测一种可变剪接的mRNA在小鼠和人类中可翻译为一种假定的可溶性α-klotho蛋白,其仅具有代表“剪接的α-klotho Kl1”(spKl1)的Kl1结构域,并且在没有膜靶向或切割的情况下从细胞中释放。这种蛋白质的存在已经有二十年了。我们针对15个氨基酸的表位(E15;VSPLTKPSVGLLLPH)产生了一种新型抗体(抗spE15),该表位不存在于Kl1或全长α-klotho中,并在体外验证了其对spKl1的特异性反应性。使用抗spE15和两种成熟的抗α-klotho单克隆抗体,我们进行了免疫印迹、免疫沉淀和免疫组织化学,以研究spKl1在小鼠脑中的表达。我们在小鼠脑中发现了抗spE15标记,但未能在同一蛋白质上看到Kl1和spE15表位的共标记,这是spKl1多肽存在的先决条件,表明抗spE15可能与假定的spKl1以外的另一种蛋白质结合。在从小鼠脑中分离的脉络丛中,我们发现抗spE15有强烈染色,但未发现剪接的α-klotho转录本。我们得出结论,使用可靠的试剂并纳入适当的对照,没有证据表明小鼠脑中存在spKl1蛋白。