Granulomas form as a conserved host response to a variety of inflammatory and infectious stimuli. As granulomas assemble, macrophages interdigitate and undergo a striking morphological transition, taking on an epithelioid appearance. The basis for this transformation and the consequences for disease are not fully understood. We have identified a conserved reprogramming of macrophages that underlies the assembly and stability of mycobacterial granulomas. Using a zebrafish model, we find that epithelial modules and structures are induced during granuloma formation and are critical for granuloma integrity. In this project we will 1) use long-term intravital imaging to assess key epithelial modules engaged by macrophages during granuloma formation and how disruption of the mycobacterial granuloma can lead to improved host outcome; 2) test the role of the IL-4/IL-13/Stat6 axis during macrophage reprogramming events; 3) based on RNA-seq analysis of macrophages isolated from infected animals, assess the role of the sonic hedgehog (Shh) pathway in granuloma formation, maintenance, and infection trajectory. Findings from this project will be translated into human disease. Overall, this proposal will test the hypothesis that, in a striking parallel to mesenchymal-to- epithelial transitions in cancer, macrophages draw on classical developmental signaling pathways to undergo an epithelial-like transition and construct the central structure of tuberculosis. A new perspective on this critical structure may have important implications for our understanding of disease progression and the design of new therapeutic approaches.

Public Health Relevance

This project will investigate the granuloma, an organized aggregate of immune cells that forms in response to certain inflammatory stimuli, including infections with the bacteria that cause tuberculosis. The project aims to understand how granulomas form and how they contribute to the growth and spread of mycobacterial diseases like tuberculosis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI130236-01
Application #
9288245
Study Section
Innate Immunity and Inflammation Study Section (III)
Program Officer
Singleton, Kentner L
Project Start
2017-03-03
Project End
2022-02-28
Budget Start
2017-03-03
Budget End
2018-02-28
Support Year
1
Fiscal Year
2017
Total Cost
$427,101
Indirect Cost
$150,572
Name
Duke University
Department
Genetics
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
Cronan, Mark R; Matty, Molly A; Rosenberg, Allison F et al. (2018) An explant technique for high-resolution imaging and manipulation of mycobacterial granulomas. Nat Methods 15:1098-1107
Walton, Eric M; Cronan, Mark R; Cambier, C J et al. (2018) Cyclopropane Modification of Trehalose Dimycolate Drives Granuloma Angiogenesis and Mycobacterial Growth through Vegf Signaling. Cell Host Microbe 24:514-525.e6
Jain, Sanjay K; Tobin, David M; Tucker, Elizabeth W et al. (2018) Tuberculous meningitis: a roadmap for advancing basic and translational research. Nat Immunol 19:521-525