2006年12月
The luminal domain participates in the endosomal trafficking of the cation-independent mannose 6-phosphate receptor
EXPERIMENTAL CELL RESEARCH
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- 巻
- 312
- 号
- 20
- 開始ページ
- 4090
- 終了ページ
- 4107
- 記述言語
- 英語
- 掲載種別
- DOI
- 10.1016/j.yexcr.2006.09.024
- 出版者・発行元
- ELSEVIER INC
Although the role of the cytoplasmic tail of the cation-independent mannose 6-phosphate receptor (CIMPR) has been well established in the receptor trafficking, that of the luminal domain is still controversial. We noticed that the peripheral distribution of GFP, fused to the transmembrane and cytoplasmic domains of CIMPR (G-CIMPR-tail), was distinct from that of endogenous CIMPR or of GFP fused to the full-length CIMPR (G-CIMPR-full). By live-cell imaging, trans-Golgi-network (TGN)-derived transport carriers containing G-CIMPR-full more frequently stopped and overlapped with transferrin-containing endosomes in the peripheral region than those containing G-CIMPR-tail. G-CIMPR-full was recycled back to the perinuclear TGN more slowly than that for G-CIMPR-tail, evidenced by fluorescence recovery after photobleaching analysis. Moreover, endogenous CIMPR and G-CIMPR-full, but not GFP-CIMPR-tail, drastically altered the characteristic distribution after treatment with chloroquine. A mutant receptor, G-CIMPR-full R/A, that cannot recognize the mannose 6-phosphate (M6P)-signal, behaved similarly to G-CIMPR-full, indicating that these differences are not attributable to the M6P-ligands binding situation. Interestingly, we also found that U18666A treatment was able to discriminate the M6P-ligand binding-dependent trafficking of CIMPR. Based on these findings, we propose that the CIMPR luminal domain is required for tight interaction with endocytic compartments, and retention by them, and that there are additional transport steps, in which the binding to M6P-ligands is involved. (c) 2006 Elsevier Inc. All rights reserved.
- リンク情報
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- DOI
- https://doi.org/10.1016/j.yexcr.2006.09.024
- CiNii Articles
- http://ci.nii.ac.jp/naid/80018762557
- PubMed
- https://www.ncbi.nlm.nih.gov/pubmed/17069798
- Web of Science
- https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000242838100012&DestApp=WOS_CPL
- ID情報
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- DOI : 10.1016/j.yexcr.2006.09.024
- ISSN : 0014-4827
- CiNii Articles ID : 80018762557
- PubMed ID : 17069798
- Web of Science ID : WOS:000242838100012