Kato Y, Arakawa E, Kinoshita S, Shirai A, Furuya A, Yamano K, Nakamura K, Iida A, Anazawa H, Koh N, Iwano A, Imura A, Fujimori T, Kuro-o M, Hanai N, Takeshige K, Nabeshima Y
Tokyo Research Laboratories, Kyowa Hakko Kogyo Co. Ltd., 3-6-6, Asahi-machi, Machida-shi, Tokyo, 194-8533, Japan.
Biochem Biophys Res Commun. 2000 Jan 19;267(2):597-602. doi: 10.1006/bbrc.1999.2009.
A novel gene, klotho (kl), which is involved in the development of a syndrome resembling human aging in mice, was recently identified. The kl gene encodes a single-pass membrane protein whose extracellular domain carries homology to beta-glucosidases. There also exists a splice variant of kl mRNA which encodes a putative secreted protein in both human and mouse. In this study, to characterize the physiological roles of Klotho protein, we established three monoclonal antibodies (mAbs) against the recombinant human Klotho protein. The mAbs are named KM2076 (rat IgG(2)a), KM2119 (rat IgG(2)b), and KM2365 (mouse IgG(1)). In Western blots, KM2076 and KM2119 specifically recognized a 130 kDa Klotho protein in the mouse and human kidney membrane fractions. To detect the human Klotho protein, the sandwich-type ELISA system with KM2076 and KM2365 was established. Using the ELISA system, we detected the human Klotho protein as low as 20 ng/ml in the supernatant of Chinese hamster ovary cells (CHO cells), introduced the human klotho gene. KM2076 and KM2119 specifically gave a positive staining by immunohistochemical staining in paraffin or frozen sections of the kidneys from wild-type mice but not in those from kl mice. Strong staining was observed especially in cortical renal tubules of the mouse kidney, where expression of klotho transcripts overlaps. KM2076 also showed a similar reaction pattern in the paraffin sections of rat and human kidneys. The mAbs established in this paper will serve as useful analytical, pathological, and diagnostic tools to disclose the role of Klotho protein in the suppression of a syndrome resembling human aging.
最近发现了一种新基因——klotho(kl),它与小鼠中类似人类衰老的综合征的发生有关。kl基因编码一种单次跨膜蛋白,其胞外结构域与β-葡萄糖苷酶具有同源性。在人和小鼠中还存在kl mRNA的剪接变体,其编码一种假定的分泌蛋白。在本研究中,为了表征Klotho蛋白的生理作用,我们制备了三种针对重组人Klotho蛋白的单克隆抗体(mAb)。这些单克隆抗体分别命名为KM2076(大鼠IgG(2)a)、KM2119(大鼠IgG(2)b)和KM2365(小鼠IgG(1))。在蛋白质免疫印迹分析中,KM2076和KM2119在小鼠和人肾膜组分中特异性识别出130 kDa的Klotho蛋白。为了检测人Klotho蛋白,建立了使用KM2076和KM2365的夹心型酶联免疫吸附测定(ELISA)系统。利用该ELISA系统,我们在导入人klotho基因的中国仓鼠卵巢细胞(CHO细胞)的上清液中检测到低至20 ng/ml的人Klotho蛋白。KM2076和KM2119在野生型小鼠肾脏的石蜡或冰冻切片中通过免疫组织化学染色特异性地呈现阳性染色,而在kl基因敲除小鼠的肾脏切片中则没有。在小鼠肾脏的皮质肾小管中观察到强染色,而klotho转录本的表达与之重叠。KM2076在大鼠和人肾脏的石蜡切片中也显示出类似的反应模式。本文制备的单克隆抗体将作为有用的分析、病理和诊断工具,以揭示Klotho蛋白在抑制类似人类衰老综合征中的作用。