Regulation of Adipose-Lymphatic Cross-talk

NIH RePORTER · NIH · R01 · $462,001 · view on reporter.nih.gov ↗

Abstract

ABSTRACT Adipose tissue is complex and heterogenous, containing numerous structures and cell types besides adipocytes. This includes lymphatic vessels, which return interstitial fluid, solutes, and immune cells back to circulation. There is a well-documented but unexplained bidirectional relationship between adipocytes and lymphatic vessels, such that poor lymphatic function leads to increased adiposity. Conversely, obesity results in impaired lymphatic flow. The molecular basis for these interactions is unknown. Our single cell RNA sequencing data from mouse and human adipose tissue revealed that lymphatic endothelial cells express the neuropeptide neurotensin (NTS). We show that NTS is a potent anti-thermogenic agent, and its expression is suppressed by cold temperatures. Here we will characterize the mechanisms regulating NTS expression and processing, and we will utilize state of the art techniques to document the effects of losing NTS in lymphatic vessels or its receptor on adipocytes. These studies will help explain the puzzling relationship between fat and the lymphatic system, and will also lead to new insights into control of adipose physiology and metabolism by neuropeptides.

Key facts

NIH application ID
10834889
Project number
5R01DK126789-04
Recipient
BETH ISRAEL DEACONESS MEDICAL CENTER
Principal Investigator
Evan D Rosen
Activity code
R01
Funding institute
NIH
Fiscal year
2024
Award amount
$462,001
Award type
5
Project period
2021-07-15 → 2026-04-30