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Lymphatic endothelial cells promote T lymphocyte migration into lymph nodes under hyperlipidemic conditions

Title
Lymphatic endothelial cells promote T lymphocyte migration into lymph nodes under hyperlipidemic conditions
Authors
Park, MinhwaCho, Kyung-AhKim, Yu-HeeLee, Kyung HoWoo, So-Youn
Ewha Authors
우소연김유희조경아
SCOPUS Author ID
우소연scopus; 김유희scopus; 조경아scopus
Issue Date
2020
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
ISSN
0006-291XJCR Link

1090-2104JCR Link
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS vol. 525, no. 3, pp. 786 - 792
Keywords
HyperlipidemiaLymphatic endothelial cellsChemokineT cell migration
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Indexed
SCIE; SCOPUS WOS scopus
Document Type
Article
Abstract
Lymphatic vessels serve as conduits through which immune cells traffic. Because lymphatic vessels are also involved in lipid transport, their function is vulnerable to abnormal metabolic conditions such as obesity and hyperlipidemia. Exactly how these conditions impact immune cell trafficking, however, is not well understood. Here, we found higher numbers of LYVE-1-positive lymphatic endothelial cells and CD3-positive T cells in the lymph nodes of mice fed high-cholesterol or high-fat diets compared with those of mice fed a normal chow diet. To confirm the effect of fat content on immune cell trafficking, the lymphatic endothelial SVEC4-10 cell line was treated with palmitic acid at a 100 mu M concentration. After 24 h, palmitic acid-treated cells exhibited increased expression of podoplanin and vascular growth-associated molecules (VEGFC, VEGFD, VEGFR3, and NRP2) and enhanced tube formation. Microarray analysis showed an increase in pro-inflammatory cytokine and chemokine transcription after palmitic acid treatment. Finally, transwell migration assay confirmed that T cell line moved toward medium previously cultured with palmitic acid-treated SVEC4-10 cells. Together, our results suggest that hyperlipidemia drives lymphatic vessel remodeling and T cell migration toward lymphatic endothelial cells. (C) 2020 Elsevier Inc. All rights reserved.
DOI
10.1016/j.bbrc.2020.02.154
Appears in Collections:
의과대학 > 의학과 > Journal papers
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