Regulation of Atherosclerosis Development by Neurotensin Derived From Lymphatic Endothelial Cells in Mice.
Regulation of Atherosclerosis Development by Neurotensin Derived From Lymphatic Endothelial Cells in Mice.
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DOI:
10.1161/atvbaha.123.319527
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发表时间:
2023-09
影响因子:
8.7
通讯作者:
Li, Jin
中科院分区:
文献类型:
--
作者:
Liu, Cenxi;Xiong, Xuelian;Li, Jin
NTS (neurotensin) is a 13-amino acid peptide that interacts with NTSR1 (neurotensin receptor), NTSR2, or SORT1 (sortilin) proteins. Studies have shown positive correlations between NTS and the development of cardiovascular diseases. 1, 2 However, constitutive depletion of Nts in the mice is not suitable for investigating this topic, given the diverse effects of NTS on body temperature and food intake by regulating the central nervous system. The data that support the findings of this study are available from the corresponding author upon reasonable request.The lymphatic system, a part of the circulation system, transports the immune cells and lipids. Lymphatic endothelial cells (LECs) also secrete various proteins, such as REELIN, which may be important for the cardiovascular system. 3 Understanding the physiological functions of these secretory proteins is a research highlight in vascular biology. Our previous studies have shown that LECs secrete NTS in various tissues, including adipose tissues, skin, and liver. 4, 5 To investigate the effects of LEC-derived NTS on atherosclerosis development, we developed an inducible Nts knockout mouse model (C57BL6/J) restricted