LRRK2 and Rab10 coordinate macropinocytosis to mediate immunological responses in phagocytes

EMBO J. 2020 Oct 15;39(20):e104862. doi: 10.15252/embj.2020104862. Epub 2020 Aug 27.

Abstract

Genetic variation in LRRK2 associates with the susceptibility to Parkinson's disease, Crohn's disease, and mycobacteria infection. High expression of LRRK2 and its substrate Rab10 occurs in phagocytic cells in the immune system. In mouse and human primary macrophages, dendritic cells, and microglia-like cells, we find that Rab10 specifically regulates a specialized form of endocytosis known as macropinocytosis, without affecting phagocytosis or clathrin-mediated endocytosis. LRRK2 phosphorylates cytoplasmic PI(3,4,5)P3-positive GTP-Rab10, before EEA1 and Rab5 recruitment to early macropinosomes occurs. Macropinosome cargo in macrophages includes CCR5, CD11b, and MHCII, and LRRK2-phosphorylation of Rab10 potently blocks EHBP1L1-mediated recycling tubules and cargo turnover. EHBP1L1 overexpression competitively inhibits LRRK2-phosphorylation of Rab10, mimicking the effects of LRRK2 kinase inhibition in promoting cargo recycling. Both Rab10 knockdown and LRRK2 kinase inhibition potently suppress the maturation of macropinosome-derived CCR5-loaded signaling endosomes that are critical for CCL5-induced immunological responses that include Akt activation and chemotaxis. These data support a novel signaling axis in the endolysosomal system whereby LRRK2-mediated Rab10 phosphorylation stalls vesicle fast recycling to promote PI3K-Akt immunological responses.

Keywords: LRRK2; Rab10; macropinocytosis; phagocytosis; phosphorylation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Carrier Proteins / metabolism*
  • Cell Membrane / metabolism
  • Chemokine CCL5 / pharmacology
  • Chemotaxis / genetics
  • Dendritic Cells / metabolism
  • Endosomes / drug effects
  • Endosomes / metabolism
  • Female
  • Gene Knockdown Techniques
  • Humans
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 / genetics
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 / metabolism*
  • Macrophages / drug effects
  • Macrophages / metabolism*
  • Male
  • Mass Spectrometry
  • Mice
  • Mice, Transgenic
  • Microglia / metabolism
  • Monocytes / drug effects
  • Monocytes / metabolism
  • Mutation
  • Phagocytes / drug effects
  • Phagocytes / immunology*
  • Phagocytes / metabolism
  • Phosphorylation
  • Pinocytosis / drug effects
  • Pinocytosis / genetics*
  • Protein Binding
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction / genetics
  • rab GTP-Binding Proteins / genetics
  • rab GTP-Binding Proteins / metabolism*

Substances

  • Carrier Proteins
  • Chemokine CCL5
  • EHBP1L1 protein, mouse
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Lrrk2 protein, mouse
  • Proto-Oncogene Proteins c-akt
  • Rab10 protein, mouse
  • rab GTP-Binding Proteins