PUBLICATION
Leptin regulates glucose homeostasis via the canonical Wnt pathway in the zebrafish
- Authors
- Kamstra, K., Rizwan, M.Z., Grattan, D.R., Horsfield, J.A., Tups, A.
- ID
- ZDB-PUB-220222-11
- Date
- 2022
- Source
- FASEB journal : official publication of the Federation of American Societies for Experimental Biology 36: e22207 (Journal)
- Registered Authors
- Horsfield, Jules
- Keywords
- CRISPR Cas9, glucose tolerance test, leptin receptor, leptin-a, leptin-b, lithium chloride
- MeSH Terms
-
- Wnt Signaling Pathway*
- Zebrafish
- Homeostasis
- Receptors, Leptin/genetics
- Receptors, Leptin/metabolism
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism
- Glucose/metabolism*
- Hyperglycemia/metabolism*
- Animals
- Leptin/genetics
- Leptin/metabolism*
- PubMed
- 35188286 Full text @ FASEB J.
Citation
Kamstra, K., Rizwan, M.Z., Grattan, D.R., Horsfield, J.A., Tups, A. (2022) Leptin regulates glucose homeostasis via the canonical Wnt pathway in the zebrafish. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 36:e22207.
Abstract
Leptin is best known for its role in adipostasis, but it also regulates blood glucose levels. The molecular mechanism by which leptin controls glucose homeostasis remains largely unknown. Here, we use a zebrafish model to show that Wnt signaling mediates the glucoregulatory effects of leptin. Under normal feeding conditions, leptin regulates glucose homeostasis but not adipostasis in zebrafish. In times of nutrient excess, however, we found that leptin also regulates body weight and size. Using a Wnt signaling reporter fish, we show that leptin activates the canonical Wnt pathway in vivo. Utilizing two paradigms for hyperglycemia, it is revealed that leptin regulates glucose homeostasis via the Wnt pathway, as pharmacological inhibition of this pathway impairs the glucoregulatory actions of leptin. Our results may shed new light on the evolution of the physiological function of leptin.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping