Neuroglobin and cytoglobin - Fresh blood for the vertebrate globin family

被引:233
作者
Pesce, A
Bolognesi, M
Bocedi, A
Ascenzi, P
Dewilde, S
Moens, L
Hankeln, T
Burmester, T
机构
[1] Univ Genoa, Dept Phys, INFM, I-16146 Genoa, Italy
[2] Univ Genoa, Ctr Excellence Biomed Res, I-16146 Genoa, Italy
[3] Univ Roma Tre, Dept Biol, I-00146 Rome, Italy
[4] Univ Antwerp, Dept Biochem, B-2610 Antwerp, Belgium
[5] Johannes Gutenberg Univ Mainz, Inst Genet Mol, D-55099 Mainz, Germany
[6] Johannes Gutenberg Univ Mainz, Inst Zool, D-55099 Mainz, Germany
关键词
D O I
10.1093/embo-reports/kvf248
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neuroglobin and cytoglobin are two recently discovered members of the vertebrate globin family. Both are intracellular proteins endowed with hexacoordinated heme-Fe atoms, in their ferrous and ferric forms, and display O-2 affinities comparable with that of myoglobin. Neuroglobin, which is predominantly expressed in nerve cells, is thought to protect neurons from hypoxic-ischemic injury. It is of ancient evolutionary origin, and is homologous to nerve globins of invertebrates. Cytoglobin is expressed in many different tissues, although at varying levels. It shares common ancestry with myoglobin, and can be traced to early vertebrate evolution. The physiological roles of neuroglobin and cytoglobin are not completely understood. Although supplying cells with O-2 is the likely function, it is also possible that both globins act as O-2-consuming enzymes or as 0, sensors. Here, we review what is currently known about neuroglobin and cytoglobin in terms of their function, tissue distribution and relatedness to the well-known hemoglobin and myoglobin. Strikingly, the data reveal that O-2 metabolism in cells is more complicated than was thought before, requiring unexpected O-2-binding proteins with potentially novel functional features.
引用
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页码:1146 / 1151
页数:6
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