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Completed NON-SBIR/STTR RPGS NIH (US)

Role of membrane-associated macrophages in health and inflammation

$3.98M USD

Funder NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
Recipient Organization University of Illinois At Chicago
Country United States
Start Date Jan 01, 2021
End Date Nov 30, 2025
Duration 1,794 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10747378
Grant Description

PROJECT SUMMARY/ ABSTRACT Mesenteritis is an inflammatory disorder of mesenteric tissues. It includes mesenteric lipodystrophy (mesenteric fat necrosis), mesenteric panniculitis (chronic mesenteric fibrosis) and mesenteric lymphadentis (mesenteric lymph node inflammation). It is diagnosed by an abdominal

computed tomography (CT) scan; however, the cause of mesenteritis remains unknown. Emerging clinical evidence shows that mesenteritis is associated with gut inflammation such as IBD and Chron's Disease. As innate myeloid cells, macrophages are distributed throughout the whole organism and they play crucial roles in mediating tissue inflammation. Based on our

supporting data, we identified macrophage populations in serous membrane of gut mesentery (termed membrane-associated macrophages). Thus, this research proposal seeks to address fundamental questions regarding the tissue specific role of membrane-associated macrophages in steady state and during mesenteritis induced gut inflammation. These include how membrane-

associated macrophages are reprogrammed by local niches and gut inflammation. To better describe the role of these macrophages and its mechanism, we performed genetic studies of membrane-associated macrophages that provided insight into their roles in steady state and gut inflammation. These preliminary data results have led us to pursue to the following specific aims:

(1) Determine distinct homeostatic functions of membrane-associated macrophages and local signals that shape their tissue specification; (2) Determine the role of membrane- associated macrophages during mesenteritis induced by gut inflammation. We will perform lineage tracing, cell ablation, transcriptomic analysis of membrane-associated macrophages and

in vivo live imaging to understand the role and dynamic interactions of macrophages with local environment in steady state and during mesenteritis induced by gut inflammation. Ultimately, we hope our studies will lead to the discovery of therapeutic targets to prevent mesenteritis as well as gut inflammation.

All Grantees

University of Illinois At Chicago

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