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

Title
dNP2 is a blood-brain barrier-permeable peptide enabling ctCTLA-4 protein delivery to ameliorate experimental autoimmune encephalomyelitis
Authors
Sangho LimWon-Ju KimYeon-Ho KimSohee LeeJa-Hyun KooJung-Ah LeeHeeseok YoonDo-Hyun KimHong-Jai ParkKim, HMHong-Gyun LeeJi Yun KimJae-Ung LeeJae Hun ShinLark Kyun KimDoh, JHye-Mi KimLee, SKBothwell, ALMSuh, MChoi, JM
Date Issued
2015-09
Publisher
Macmillan Publishers Limited. All rights reserved
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.
Keywords
cytoplasmic domain of cytotoxic T lymphocyte antigen 4; cytotoxic T lymphocyte antigen 4; neuroprotective agent; peptide derivative; recombinant dNP2; recombinant protein; unclassified drug; blood; cytology; cytoplasm; drug; experimental study; immune response; peptide; permeability; protein; rodent; animal cell; animal experiment; animal model; Article; blood brain barrier; CD4+ T lymphocyte; cell permeabilization; central nervous system; confocal microscopy; controlled study; demyelination; drug conjugation; drug penetration; experimental autoimmune encephalomyelitis; female; fluorescence microscopy; HeLa cell line; human; human cell; inflammatory disease; mouse; mouse model; multiple sclerosis; neuroprotection; nonhuman; T lymphocyte; tandem repeat; Th1 cell; Th17 cell
URI
https://oasis.postech.ac.kr/handle/2014.oak/13458
DOI
10.1038/NCOMMS9244
ISSN
2041-1723
Article Type
Article
Citation
NATURE COMMUNICATIONS, vol. 6, page. 8244, 2015-09
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도준상DOH, JUN SANG
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