4.6 Article

Mapping and targeted viral activation of pancreatic nerves in mice reveal their roles in the regulation of glucose metabolism

Journal

NATURE BIOMEDICAL ENGINEERING
Volume 6, Issue 11, Pages 1298-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41551-022-00909-y

Keywords

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Funding

  1. Charles H. Revson Foundation [18-25]
  2. Swedish Society for Medical Research (SSMF)
  3. NIH [T32GM007280, F31DK129016]
  4. Naomi Berries Diabetes Center Russell Berrie Foundation Award
  5. American Diabetes Association Pathway to Stop Diabetes Grant ADA [1-17-ACE-31]
  6. National Institutes of Health [R01NS097184, OT2OD024912, R01DK124461]
  7. Department of Defense [W81XWH-20-1-0345, W81XWH-20-1-0156]
  8. JPB Foundation
  9. NIDDK-supported Einstein-Sinai Diabetes Research Center (DRC) [P-30 DK020541]

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The mapping and activation of pancreatic nerves through tissue clearing, retrograde tracing, and viral gene delivery facilitates the study of glucose metabolism regulation. Targeting parasympathetic pancreatic neurons increases plasma-insulin levels and improves glucose tolerance in male mice, while stimulating sympathetic neurons impairs tolerance.
A lack of comprehensive mapping of ganglionic inputs into the pancreas and of technology for the modulation of the activity of specific pancreatic nerves has hindered the study of how they regulate metabolic processes. Here we show that the pancreas-innervating neurons in sympathetic, parasympathetic and sensory ganglia can be mapped in detail by using tissue clearing and retrograde tracing (the tracing of neural connections from the synapse to the cell body), and that genetic payloads can be delivered via intrapancreatic injection to target sites in efferent pancreatic nerves in live mice through optimized adeno-associated viruses and neural-tissue-specific promoters. We also show that, in male mice, the targeted activation of parasympathetic cholinergic intrapancreatic ganglia and neurons doubled plasma-insulin levels and improved glucose tolerance, and that tolerance was impaired by stimulating pancreas-projecting sympathetic neurons. The ability to map the peripheral ganglia innervating the pancreas and to deliver transgenes to specific pancreas-projecting neurons will facilitate the examination of ganglionic inputs and the study of the roles of pancreatic efferent innervation in glucose metabolism. Tissue clearing, retrograde tracing and viral gene delivery to target sites in pancreas-innervating ganglia in mice facilitate the mapping and activation of pancreatic nerves and the study of how they regulate glucose metabolism.

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