Regulation of Type 1 Diabetes via Brown Adipocyte–Secreted Proteins and the Novel Glucagon Regulator Nidogen-2
Large embryonic brown adipose tissue-secreted proteins (CB-100) suppress glucagon and normalize glycemia in mice with type 1 diabetes (T1D) without changing insulin. CB-100 prevented T1D-induced whitening, promoted browning of adipose tissue, and enhanced glucose uptake via an insulin receptor-dependent pathway. Within CB-100, nidogen-2 regulated glucagon secretion and restored euglycemia in T1D. Nidogen-2 and CB-100 unveil a therapeutic strategy for diabetes management beyond insulin-centric paradigms by modulating glucagon secretion and enhancing glucose metabolism.
Authors
- David W. Piston (ORCID: https://orcid.org/0000-0002-1200-3116)
- Dennis Goldfarb (ORCID: https://orcid.org/0000-0002-1584-5423)
- Emily Wilkerson (ORCID: https://orcid.org/0000-0002-9360-7340)
- Debbie C. Thurmond (ORCID: https://orcid.org/0000-0002-6303-4596)
- Alessandro Ustione
- Rekha Balakrishnan (ORCID: https://orcid.org/0000-0002-9724-5578)
- Jeongmin Lee (ORCID: https://orcid.org/0000-0003-2554-4285)
Institutions
- Washington University in St. Louis (US)
- City of Hope (US)
Publication Details
- Journal
- Diabetes
- Published
- 2025-02-28
- DOI
- https://doi.org/10.2337/db24-1003
- Citations
- 1
- Primary Topic
- Adipose Tissue and Metabolism
- Type
- article
- Field-Weighted Citation Impact
- 1.16