Separation of subcellular compartments containing distinct functional forms of MHC class II
about
A role for MHC class II antigen processing in B cell development.B lymphocytes secrete antigen-presenting vesiclesDendritic cells use macropinocytosis and the mannose receptor to concentrate macromolecules in the major histocompatibility complex class II compartment: downregulation by cytokines and bacterial productsA conserved signal and GTPase complex are required for the ciliary transport of polycystin-1.The enhanced immune response to the HIV gp160/LAMP chimeric gene product targeted to the lysosome membrane protein trafficking pathwayA role for acidic residues in di-leucine motif-based targeting to the endocytic pathwayDirect vesicular transport of MHC class II molecules from lysosomal structures to the cell surfaceNegative regulation by HLA-DO of MHC class II-restricted antigen processingEndocytic sequestration of the B cell antigen receptor and toll-like receptor 9 in anergic cells.Phagocytic antigen processing and effects of microbial products on antigen processing and T-cell responses.Production, specificity, and functionality of monoclonal antibodies to specific peptide-major histocompatibility complex class II complexes formed by processing of exogenous protein.Mtv-1 superantigen trafficks independently of major histocompatibility complex class II directly to the B-cell surface by the exocytic pathway.Intracellular traffic to compartments for MHC class II peptide loading: signals for endosomal and polarized sorting.Intracellular transport and peptide loading of MHC class II molecules: regulation by chaperones and motors.Extending the CD4(+) T-cell epitope specificity of the Th1 immune response to an antigen using a Salmonella enterica serovar typhimurium delivery vehicle.Pulse-chase analysis for studies of MHC class II biosynthesis, maturation, and peptide loading.Phagocytic processing of antigens for presentation by class II major histocompatibility complex molecules.PBP74, a new member of the mammalian 70-kDa heat shock protein family, is a mitochondrial protein.Role of phagosomes and major histocompatibility complex class II (MHC-II) compartment in MHC-II antigen processing of Mycobacterium tuberculosis in human macrophages."Troy-bodies": recombinant antibodies that target T cell epitopes to antigen presenting cells.Efficient endosomal localization of major histocompatibility complex class II-invariant chain complexes requires multimerization of the invariant chain targeting sequence.Rab 7: an important regulator of late endocytic membrane trafficIsoforms of the invariant chain regulate transport of MHC class II molecules to antigen processing compartmentsSequential actions of Rab5 and Rab7 regulate endocytosis in the Xenopus oocyte.Mutant Rab7 causes the accumulation of cathepsin D and cation-independent mannose 6-phosphate receptor in an early endocytic compartmentRight place, right time, right peptide: DO keeps DM focused.Ii chain controls the transport of major histocompatibility complex class II molecules to and from lysosomes.Live Salmonella recruits N-ethylmaleimide-sensitive fusion protein on phagosomal membrane and promotes fusion with early endosome.The requirement for DM in class II-restricted antigen presentation and SDS-stable dimer formation is allele and species dependent.Invariant chain cleavage and peptide loading in major histocompatibility complex class II vesicles.Detection of functional class II-associated antigen: role of a low density endosomal compartment in antigen processingIntracellular targeting of antigens internalized by membrane immunoglobulin in B lymphocytes.Inhibition of invariant chain (Ii)-calnexin interaction results in enhanced degradation of Ii but does not prevent the assembly of alpha beta Ii complexesA structural transition in class II major histocompatibility complex proteins at mildly acidic pH.Processing of Mycobacterium tuberculosis antigen 85B involves intraphagosomal formation of peptide-major histocompatibility complex II complexes and is inhibited by live bacilli that decrease phagosome maturation.Related leucine-based cytoplasmic targeting signals in invariant chain and major histocompatibility complex class II molecules control endocytic presentation of distinct determinants in a single protein.HLA-DM interactions with intermediates in HLA-DR maturation and a role for HLA-DM in stabilizing empty HLA-DR moleculesDegradation of mouse invariant chain: roles of cathepsins S and D and the influence of major histocompatibility complex polymorphismNovel mutants define genes required for the expression of human histocompatibility leukocyte antigen DM: evidence for loci on human chromosome 6pA lysosomal targeting signal in the cytoplasmic tail of the beta chain directs HLA-DM to MHC class II compartments.
P2860
Q22305702-F463140E-C424-4EC4-8FC7-6F8C03C2F316Q24678522-3E6D6E9D-C4EC-4056-AEC2-BE4A029B2DF6Q24678867-28AFCBB8-3A4B-4DC4-9EBF-DA52F1DE016CQ28000060-813BECBD-A634-4735-B728-CBAAD66A38CAQ28306549-E050FA0C-1E4D-4078-B6C8-12ED31437F8BQ28612864-C8B39E59-8685-423C-91CD-3B60281E5CF0Q28613123-76C43488-D5C5-40D3-9B34-91A2875A64A1Q28613199-9FD623F0-4D62-4780-854B-EB45764AF865Q30486747-1043FD1E-75AC-439F-9B16-AEC41E719A86Q33683408-EF0B1F67-C7F1-473B-8F35-AE58567EE8FCQ33731623-51A42C13-4DE0-445D-9F50-336B8B3FAB3CQ33782938-346F3206-86CD-4999-8B02-EC7C45B40BFBQ33815419-487F6B61-24B1-405A-9088-2BD9AF303F7AQ33815425-2672FF9B-5F7A-4F90-A83F-60DCD43A30BAQ34004518-AF2C0B5E-7362-41CA-9401-C51883B81804Q34155809-26EEEBC3-67EB-4DA3-85BC-37CF5EFD49C2Q34156238-907CB825-B9FA-4875-BA87-757011E6B874Q34446048-DA6BDB1E-0771-4061-8AFE-1A5ECA2C48C9Q34491781-408EC56B-2E35-4805-9561-A583D1A91D95Q34560537-008F83DA-DB93-4EC0-B68F-A6C32EB88ED4Q36235619-2291B21C-7F6D-4681-B4E6-F0237AA558FAQ36236377-81766B5A-2126-4DE0-9B2D-240CD8632E49Q36236708-AE5A431C-ACAA-4728-B5B8-0C5C8316EFE4Q36254673-B18F46E4-C780-4595-95DA-A795C8CF9DEFQ36255234-122743E0-61C5-46EF-85FC-6B247B542324Q36266508-C00BB801-AC37-4124-941F-13E1B5F2EB6FQ36274077-9BB2517F-339E-43EB-A67E-6FB6129B5269Q36316409-FE259562-EDEE-4336-BFF6-862F516FEC66Q36364225-9819E7FC-8614-41B8-8708-19CD95139CD9Q36364770-91B2A451-2E7F-4867-9D15-0DCC1DE9A326Q36364817-96C6C04E-2E98-4B90-8599-84E6A8D36E2CQ36364863-E20C24A4-63B3-4143-B48E-E486928F9AEEQ36365643-C95DE5E4-ACDB-43D5-800A-642BACB45E4CQ36366080-682BDF08-8340-43FD-8577-54B0FD019C31Q36370092-ECC0C48E-5595-4680-AFD8-49441D51BE2CQ36376527-C4942EFA-087C-42D1-8897-00CCF14D3576Q36377428-B9DD38F6-6FE4-43FC-8832-4C6FC4E6E23DQ36380525-78BA5D64-AAC9-42E6-94DB-3F75FDB5670FQ36380786-A581C50E-D7AD-4E9B-9990-CB704D31CDA1Q36382769-C1E10BA4-8CF3-4564-916D-456599BD6BC8
P2860
Separation of subcellular compartments containing distinct functional forms of MHC class II
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Separation of subcellular comp ...... nctional forms of MHC class II
@ast
Separation of subcellular comp ...... nctional forms of MHC class II
@en
type
label
Separation of subcellular comp ...... nctional forms of MHC class II
@ast
Separation of subcellular comp ...... nctional forms of MHC class II
@en
prefLabel
Separation of subcellular comp ...... nctional forms of MHC class II
@ast
Separation of subcellular comp ...... nctional forms of MHC class II
@en
P2093
P2860
P356
P1476
Separation of subcellular comp ...... nctional forms of MHC class II
@en
P2093
P2860
P304
P356
10.1083/JCB.125.3.595
P407
P577
1994-05-01T00:00:00Z