Browse

염증성 암세포에서의 caspase-8에 의존적인 lysyl-tRNA synthetase의 exosome을 통한 분비 기전 연구
Caspase-8-dependent exosomic secretion of lysyl-tRNA synthetase from inflammatory cancer

Cited 0 time in Web of Science Cited 0 time in Scopus
Authors
김상범
Advisor
김성훈
Major
융합과학기술대학원 분자의학 및 바이오제약학과
Issue Date
2017-08
Publisher
서울대학교 융합과학기술대학원
Keywords
exosomelysyl-trna synthetasesyntenincaspase-8inflammation
Description
학위논문 (박사)-- 서울대학교 융합과학기술대학원 분자의학 및 바이오제약학과, 2017. 8. 김성훈.
Abstract
Although lysyl-tRNA synthetase (KRS), an enzyme for protein synthesis, is secreted from cancer cells to trigger inflammatory responses, its secretion mechanism is not understood. Here we show that KRS is secreted via exosomes from cancer cells. KRS is located within the lumen of exosomes and released from the exosomes that are ruptured near the target cells. The N-terminal 12 amino acid of KRS was cleaved by caspase-8 upon starvation. The N-terminal cleavage exposed the PDZ-binding motif located in its C-terminal end. Syntenin bound to the exposed PDZ-binding motif of KRS and facilitated the dissociation of KRS from multi-tRNA synthetase complex for exosomic secretion. The isolated KRS-containing exosomes induced migration and TNF-α secretion of macrophages and KRS showed significant contribution to these activities. These results suggest exosomes as a secretion vehicle for KRS and its functional connection with caspase-8-mediated inflammation provoked by cancer cells.
Language
English
URI
http://hdl.handle.net/10371/137038
Files in This Item:
Appears in Collections:
Graduate School of Convergence Science and Technology (융합과학기술대학원)Molecular Medicine & Biopharmaceutical Sciences(분자의학 및 바이오제약학과)Theses (Ph.D. / Sc.D._분자의학 및 바이오제약학과)
  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse