Cytoophidia coupling adipose architecture and metabolism

Cell Mol Life Sci. 2022 Oct 1;79(10):534. doi: 10.1007/s00018-022-04567-w.

Abstract

Tissue architecture determines its unique physiology and function. How these properties are intertwined has remained unclear. Here we show that the metabolic enzyme CTP synthase (CTPS) form filamentous structures termed cytoophidia along the adipocyte cortex in Drosophila adipose tissue. Loss of cytoophidia, whether due to reduced CTPS expression or a point mutation that specifically abrogates its polymerization ability, causes impaired adipocyte adhesion and defective adipose tissue architecture. Moreover, CTPS influences integrin distribution and dot-like deposition of type IV collagen (Col IV). Col IV-integrin signaling reciprocally regulates the assembly of cytoophidia in adipocytes. Our results demonstrate that a positive feedback signaling loop containing both cytoophidia and integrin adhesion complex couple tissue architecture and metabolism in Drosophila adipose tissue.

Keywords: CTP synthase; Cell adhesion; Drosophila; Fat body; Integrin.

MeSH terms

  • Adipose Tissue / metabolism
  • Animals
  • Carbon-Nitrogen Ligases* / chemistry
  • Carbon-Nitrogen Ligases* / genetics
  • Carbon-Nitrogen Ligases* / metabolism
  • Collagen Type IV*
  • Drosophila / metabolism
  • Integrins

Substances

  • Carbon-Nitrogen Ligases
  • Collagen Type IV
  • Integrins