Podocytes use FcRn to clear IgG from the glomerular basement membrane

被引:192
作者
Akilesh, Shreeram [1 ]
Huber, Tobias B. [1 ]
Wu, Hui [1 ]
Wang, Gary [1 ]
Hartleben, Bjoern [1 ]
Kopp, Jeffrey B. [3 ]
Miner, Jeffrey H. [2 ]
Roopenian, Derry C. [4 ]
Unanue, Emil R. [1 ]
Shaw, Andrey S. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Div Renal, St Louis, MO 63110 USA
[3] NIH, Nat Inst Diabet & Digest & Kidney Dis, Bethesda, MD 20892 USA
[4] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
Fc receptor; glomerulonephritis;
D O I
10.1073/pnas.0711515105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The glomerular filtration barrier prevents large serum proteins from being lost into the urine. It is not known, however, why the filter does not routinely clog with large proteins that enter the glomerular basement membrane (GBM). Here, we provide evidence that an active transport mechanism exists to remove immunoglobulins that accumulate at the filtration barrier. We found that FcRn, an IgG and albumin transport receptor, is expressed in podocytes and functions to internalize IgG from the GBM. Mice lacking FcRn accumulated IgG in the GEM as they aged, and tracer studies showed delayed clearance of IgG from the kidneys of FcRn-deficient mice. Supporting a role for this pathway in disease, saturating the clearance mechanism potentiated the pathogenicity of nephrotoxic sera. These studies support the idea that podocytes play an active role in removing proteins from the GBM and suggest that genetic or acquired impairment of the clearance machinery is likely to be a common mechanism promoting glomerular diseases.
引用
收藏
页码:967 / 972
页数:6
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