Mucolipin‐2 Localizes to the Arf6‐Associated Pathway and Regulates Recycling of GPI‐APs

Traffic - Tập 8 Số 10 - Trang 1404-1414 - 2007
Claudia Karacsonyi1, Anitza San Miguel, Rosa Puertollano
1Laboratory of Cell Biology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA

Tóm tắt

In mammals, the mucolipin family includes three members mucolipin‐1, mucolipin‐2, and mucolipin‐3 (MCOLN1–3). While mutations in MCOLN1 and MCOLN3 have been associated with mucolipidosis type IV and the varitint‐waddlermouse phenotype, respectively, little is known about the function and cellular distribution of MCOLN2. Here we show that MCOLN2 traffics via the Arf6‐associated pathway and colocalizes with major histocompatibility protein class I (MHCI) and glycosylphosphatidylinositol‐anchored proteins (GPI‐APs), such as CD59 in both vesicles and long tubular structures. Expression of a constitutive active Arf6 mutant, or activation of endogenous Arf6 by transfection with EFA6 or treatment with aluminum fluoride, caused accumulation of MCOLN2 in enlarged vacuoles that also contain MHCI and CD59. In addition, overexpression of MCOLN2 promoted efficient activation of Arf6 in vivo,thus suggesting that MCOLN2 may have a role in the traffic of cargo through the Arf6‐associated pathway. In support of this we found that overexpression of a MCOLN2 inactive mutant decreases recycling of CD59 to the plasma membrane. Therefore, our results indicate that MCOLN2 localizes to the Arf6‐regulated pathway and regulates sorting of GPI‐APs.

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Tài liệu tham khảo

10.1016/j.ceca.2005.06.028

10.1016/0006-291X(75)90526-4

10.1001/archneur.1976.00500120032005

Bach G, 1977, Mucopolysaccharides accumulation in cultured skin fibroblasts derived from patients with Mucolipidosis IV, Am J Hum Genet, 29, 610

10.1002/ajmg.1320120308

10.1038/ng0501-64

10.1073/pnas.062065399

10.1073/pnas.0400709101

10.1073/pnas.222425399

10.1016/j.cellimm.2005.07.001

10.1111/j.1600-0854.2006.00387.x

10.1074/jbc.M511104200

10.1146/annurev.biochem.72.121801.161800

10.1083/jcb.139.1.49

10.1083/jcb.200103107

10.1091/mbc.e04-02-0151

10.1091/mbc.E04-04-0342

10.1093/emboj/21.11.2557

10.1091/mbc.E05-06-0523

10.1128/MCB.24.22.9752-9762.2004

10.1091/mbc.02-04-0053

10.1093/emboj/18.6.1480

10.1083/jcb.200104019

10.1083/jcb.200210069

10.1242/jcs.01090

10.1111/j.1600-0854.2006.00475.x

10.1074/jbc.C400046200

10.1074/jbc.M600807200

10.1091/mbc.E05-10-0980

10.1093/emboj/cdf398

10.1074/jbc.R300026200

10.1038/nrmicro1068

10.1007/s00018-005-5428-1

10.1074/jbc.M508211200

10.1016/j.jmb.2003.09.048

10.1083/jcb.200407094

10.1038/ncb1348

10.1016/j.tcb.2004.07.010

10.1016/j.ymgme.2006.05.016

10.1038/nrm1910