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dNP2 is a blood-brain barrier-permeable peptide enabling ctCTLA-4 protein delivery to ameliorate experimental autoimmune encephalomyelitis

Authors
 Sangho Lim  ;  Won-Ju Kim  ;  Yeon-Ho Kim  ;  Sohee Lee  ;  Ja-Hyun Koo  ;  Jung-Ah Lee  ;  Heeseok Yoon  ;  Do-Hyun Kim  ;  Hong-Jai Park  ;  Hye-Mi Kim  ;  Hong-Gyun Lee  ;  Ji Yun Kim  ;  Jae-Ung Lee  ;  Jae Hun Shin  ;  Lark Kyun Kim  ;  Junsang Doh  ;  Hongtae Kim  ;  Sang-Kyou Lee  ;  Alfred L.M. Bothwell  ;  Minah Suh  ;  Je-Min Choi 
Citation
 NATURE COMMUNICATIONS, Vol.6 : 8244, 2015 
Journal Title
NATURE COMMUNICATIONS
Issue Date
2015
MeSH
Animals ; Blood-Brain Barrier/metabolism* ; CTLA-4 Antigen/immunology* ; Carrier Proteins/metabolism* ; Cell-Penetrating Peptides/metabolism* ; Disease Models, Animal ; Encephalomyelitis, Autoimmune, Experimental/immunology* ; HeLa Cells ; Humans ; In Vitro Techniques ; Jurkat Cells ; Mice ; Mice, Inbred C57BL ; Peptide Fragments/metabolism ; T-Lymphocytes/immunology* ; Th17 Cells/immunology ; Ubiquitin-Protein Ligases/metabolism
Abstract
Central nervous system (CNS)-infiltrating effector T cells play critical roles in the development and progression of multiple sclerosis (MS). However, current drugs for MS are very limited due to the difficulty of delivering drugs into the CNS. Here we identify a cell-permeable peptide, dNP2, which efficiently delivers proteins into mouse and human T cells, as well as various tissues. Moreover, it enters the brain tissue and resident cells through blood vessels by penetrating the tightly organized blood-brain barrier. The dNP2-conjugated cytoplasmic domain of cytotoxic T-lymphocyte antigen 4 (dNP2-ctCTLA-4) negatively regulates activated T cells and shows inhibitory effects on experimental autoimmune encephalomyelitis in both preventive and therapeutic mouse models, resulting in the reduction of demyelination and CNS-infiltrating T helper 1 and T helper 17 cells. Thus, this study demonstrates that dNP2 is a blood-brain barrier-permeable peptide and dNP2-ctCTLA-4 could be an effective agent for treating CNS inflammatory diseases such as MS.
Files in This Item:
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DOI
10.1038/ncomms9244
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
Yonsei Authors
Kim, Lark Kyun(김락균) ORCID logo https://orcid.org/0000-0001-5983-4470
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/157314
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