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Citation

  • Authors: Liu J. et al.
  • Year: 2023
  • Journal: Cell Rep 42 111991
  • Applications: in vitro / siRNA / INTERFERin
  • Cell type: mature Dendritic cells

Method

siRNA for mouse Extl1, Sema6d, Akap2, Apol7c, Eno3, Fndc5, Ext1, Arrb1 (β-arrestin-1) were designed and synthesized by the GenePharma (China). mDCs were transfected with siRNA using INTERFERin reagent (Polyplus) following manufacturer’s instructions. Cells were analyzed for mRNA expression to confirm interference efficiency.

Abstract

CCR7-triggered DC migration toward draining lymph nodes is critical for the initiation of protective immunity and maintenance of immune tolerance. How to promote CCR7-mediated DC migration to determine T cell responses under inflammatory and homeostatic conditions remains poorly understood. Here we demonstrate that the Extl1 (Exostosin like glycosyltransferase 1) promotes CCR7-triggered DC migration in a heparan sulfate proteoglycans (HSPG)-dependent manner. Mechanistically, Extl1 mediates HSPG production via its glycosyltransferase domain to inhibit C1q expression. Extl1/HSPG axis relieves C1q-mediated restriction of CCR7 surface expression and internalization, and thus enhances CCR7-dependent migratory signaling activation. Consequently, Extl1 is required for DC-mediated Th1 and Th17 responses in immune defense against bacterial infection and for Treg cell development in the prevention of autoimmunity. Our study adds mechanistic insights to the regulation of CCR7-triggered DC migration in immunity and tolerance and provides a potential target for the treatment of infectious and autoimmune diseases.

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