Format

Send to

Choose Destination
J Gerontol A Biol Sci Med Sci. 2018 Dec 26. doi: 10.1093/gerona/gly291. [Epub ahead of print]

Prominin-like regulates longevity and glucose metabolism via insulin signaling in Drosophila.

Author information

1
Metabolism and Neurophysiology Research Group, KRIBB, Daejeon, Korea.
2
Department of Functional Genomics, UST, Daejeon, Korea.
3
Convergence Research Center for Dementia, KIST, Seoul, Korea.

Abstract

CD133, also called Prominin-1, is a biomarker for mammalian stem cells. It is involved in cell growth, development, and tumor biology. However, the function of CD133 at the organismal level has not been investigated. In this study, we found that prominin-like (promL) loss-of-function mutant flies show an extended lifespan and metabolic defects such as increased circulating carbohydrates, lipid storage, and starvation resistance. The mRNA expression levels of Drosophila insulin-like peptides (Dilps) were reduced in loss-of-function promL mutants. Furthermore, the level of phosphorylated AKT, a downstream component of insulin signaling, was lower in promL loss-of-function mutants than in the w- control flies. Importantly, the PromL protein is predominantly expressed in the pars intercerebralis region with insulin producing cells (IPCs) of the adult brain. When we inhibited promL in IPCs, these flies showed an extended lifespan, metabolic defects, and reduced insulin signaling. These results indicate that the promL gene regulates longevity and glucose metabolism by controlling insulin signaling in Drosophila.

PMID:
30590420
DOI:
10.1093/gerona/gly291

Supplemental Content

Full text links

Icon for Silverchair Information Systems
Loading ...
Support Center