生物
血红素
原卟啉
原卟啉IX
体内
生物合成
基因剔除小鼠
血红蛋白
生物化学
细胞生物学
基因
遗传学
酶
化学
卟啉
有机化学
光动力疗法
作者
Masatatsu Yamamoto,Hiroshi Arimura,Tomoko Fukushige,Kentarou Minami,Yukihiko Nishizawa,Akihide Tanimoto,Takuro Kanekura,Masayuki Nakagawa,Shin‐ichi Akiyama,Tatsuhiko Furukawa
摘要
Abcb10, member 10 of the ABC transporter family, is reportedly a part of a complex in the mitochondrial inner membrane with mitoferrin-1 (Slc25a37) and ferrochelatase (Fech) and is responsible for heme biosynthesis in utero. However, it is unclear whether loss of Abcb10 causes pathological changes in adult mice. Here, we show that Abcb10(-/-) mice lack heme biosynthesis and erythropoiesis abilities and die in midgestation. Moreover, we generated Abcb10(F/-); Mx1-Cre mice, with Abcb10 in hematopoietic cells deleted, which showed accumulation of protoporphyrin IX and maturation arrest in reticulocytes. Electron microscopy images of Abcb10(-/-) hematopoietic cells showed a marked increase of iron deposits at the mitochondria. These results suggest a critical role for Abcb10 in heme biosynthesis and provide new insights into the pathogenesis of erythropoietic protoporphyria and sideroblastic anemia.
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