Microglial-derived C1q integrates into neuronal ribonucleoprotein complexes and impacts protein homeostasis in the aging brain

Cell. 2024 Aug 8;187(16):4193-4212.e24. doi: 10.1016/j.cell.2024.05.058. Epub 2024 Jun 27.

Abstract

Neuroimmune interactions mediate intercellular communication and underlie critical brain functions. Microglia, CNS-resident macrophages, modulate the brain through direct physical interactions and the secretion of molecules. One such secreted factor, the complement protein C1q, contributes to complement-mediated synapse elimination in both developmental and disease models, yet brain C1q protein levels increase significantly throughout aging. Here, we report that C1q interacts with neuronal ribonucleoprotein (RNP) complexes in an age-dependent manner. Purified C1q protein undergoes RNA-dependent liquid-liquid phase separation (LLPS) in vitro, and the interaction of C1q with neuronal RNP complexes in vivo is dependent on RNA and endocytosis. Mice lacking C1q have age-specific alterations in neuronal protein synthesis in vivo and impaired fear memory extinction. Together, our findings reveal a biophysical property of C1q that underlies RNA- and age-dependent neuronal interactions and demonstrate a role of C1q in critical intracellular neuronal processes.

Keywords: C1q; RNA granule; RNA-binding protein; complement; liquid-liquid phase separation; microglia; neuroimmune; neuronal translation; polysome; ribonucleoprotein complex.

MeSH terms

  • Aging* / metabolism
  • Animals
  • Brain* / metabolism
  • Complement C1q* / metabolism
  • Homeostasis*
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Microglia* / metabolism
  • Neurons* / metabolism
  • Ribonucleoproteins* / metabolism

Substances

  • Complement C1q
  • Ribonucleoproteins