Miyata Yugo, Nishimura Megumi, Nagata Aya, Jing Xu, Sultan Cheryl S, Kuribayashi Risa, Takahashi Katsuya, Lee Yongchan, Nishizawa Tomohiro, Segawa Katsumori
Department of Medical Chemistry, Medical Research Laboratory, Institute of Integrated Research, Institute of Science Tokyo, Japan.
Graduate School of Medical Life Science, Yokohama City University, Japan.
FEBS Lett. 2025 Mar;599(5):656-666. doi: 10.1002/1873-3468.15084. Epub 2024 Dec 23.
Phospholipids are asymmetrically distributed in the plasma membrane (PM), and scramblases disrupt this asymmetry by shuffling phospholipids. We recently identified mouse Tmem63b as a membrane structure-responsive scramblase. Tmem63b belongs to the TMEM63/OSCA family of ion channels; however, the conservation of the scramblase activity within this family remains unclear. We expressed human TMEM63 paralogs, TMEM63B orthologs, and plant OSCA1.1 in Tmem63b-deficient mouse pro-B cells and found that vertebrate TMEM63B orthologs exhibit scramblase activity at the PM. Previously, ten pathogenic human TMEM63B variants were identified, some of which exhibited constitutive scramblase activity. Upon expressing all variants, we found that nine variants displayed constitutive scramblase activity. These results suggest that membrane structure-responsive scramblase activity at the PM is conserved among vertebrate TMEM63B orthologs.
磷脂在质膜(PM)中呈不对称分布,而翻转酶通过打乱磷脂来破坏这种不对称性。我们最近鉴定出小鼠Tmem63b是一种对膜结构有反应的翻转酶。Tmem63b属于离子通道的TMEM63/OSCA家族;然而,该家族内翻转酶活性的保守性仍不清楚。我们在缺乏Tmem63b的小鼠前B细胞中表达了人类TMEM63旁系同源物、TMEM63B直系同源物和植物OSCA1.1,发现脊椎动物TMEM63B直系同源物在质膜处表现出翻转酶活性。此前,已鉴定出十种致病性人类TMEM63B变体,其中一些表现出组成型翻转酶活性。在表达所有变体后,我们发现有九种变体显示出组成型翻转酶活性。这些结果表明,质膜处对膜结构有反应的翻转酶活性在脊椎动物TMEM63B直系同源物中是保守的。