期刊
MOLECULAR BIOLOGY OF THE CELL
卷 20, 期 1, 页码 481-497出版社
AMER SOC CELL BIOLOGY
DOI: 10.1091/mbc.E08-08-0805
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资金
- FIRCA [TW006456]
- National Institutes of Health [R01 AG027924]
- American Health Assistance Foundation [1020746]
- Fondo Nacional de Investigacion Cient fica y Tecnologica ( FONDECYT)
- Fondo de Investigacio ' n Avanzada en Areas Prioritarias (FONDAP) [13980001]
- MIFAB
- Comision Nasional de Investigacion Cientifico y Technologico ( CONICET)
- Agencia Nacional de Promocion Cient fica y Tecnologica (ANPCyT
- Argentina)
- FOGARTY INTERNATIONAL CENTER [R03TW006456] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE ON AGING [P01AG030128, R01AG035355, R01AG027924] Funding Source: NIH RePORTER
Low-density lipoprotein receptor-related protein 1 (LRP1) is an endocytic recycling receptor with two cytoplasmic tyrosine-based basolateral sorting signals. Here we show that during biosynthetic trafficking LRP1 uses AP1B adaptor complex to move from a post-TGN recycling endosome (RE) to the basolateral membrane. Then it recycles basolaterally from the basolateral sorting endosome (BSE) involving recognition by sorting nexin 17 (SNX17). In the biosynthetic pathway, Y-29 but not N-26 from a proximal NPXY directs LRP1 basolateral sorting from the TGN. A N(26)A mutant revealed that this NPXY motif recognized by SNX17 is required for the receptor's exit from BSE. An endocytic Y(63)ATL(66) motif also functions in basolateral recycling, in concert with an additional endocytic motif (LL86,87), by preventing LRP1 entry into the transcytotic apical pathway. All this sorting information operates similarly in hippocampal neurons to mediate LRP1 somatodendritic distribution regardless of the absence of AP1B in neurons. LRP1 basolateral distribution results then from spatially and temporally segregation steps mediated by recognition of distinct tyrosine-based motifs. We also demonstrate a novel function of SNX17 in basolateral/somatodendritic recycling from a different compartment than AP1B endosomes.
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