The major histocompatibility complex-related Fc receptor for IgG (FcRn) binds albumin and prolongs its lifespan

被引:521
作者
Chaudhury, C
Mehnaz, S
Robinson, JM
Hayton, WL
Pearl, DK
Roopenian, DC
Anderson, CL
机构
[1] Ohio State Univ, Dept Internal Med, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Stat, Columbus, OH 43210 USA
[3] Ohio State Univ, Dept Pharm, Columbus, OH 43210 USA
[4] Ohio State Univ, Dept Physiol & Cell Biol, Columbus, OH 43210 USA
[5] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
antibody; transport; half-life; pharmacokinetics; metabolism;
D O I
10.1084/jem.20021829
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
The inverse relationship between serum albumin concentration and its half-life suggested to early workers that albumin would be protected from a. catabolic fate by a receptor-mediated mechanism much like that proposed for IgG. We show here that albumin binds FcRn in a pH dependent fashion, that the lifespan of albumin is shortened in FcRn-deficient mice, and that the plasma albumin concentration of FcRn-deficient mice is less than half that of wild-type mice. These results affirm the hypothesis that the major histo compatibility complex-related Fc receptor protects albumin from degradation just as it does IgG, prolonging the half-lives of both.
引用
收藏
页码:315 / 322
页数:8
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