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Cyclophilin A is an endogenous ligand for the triggering receptor expressed on myeloid cells‐2 (TREM2)

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Abstract Triggering receptor expressed on myeloid cells 2 (TREM2) is a cell surface receptor expressed on macrophages, microglial cells, and pre‐osteoclasts, and that participates in diverse cellular function, including inflammation, bone homeostasis, neurological development, and coagulation. In spite of the indispensable role of the TREM2 protein in the maintenance of immune homeostasis and osteoclast differentiation, the exact ligand for TREM2 has not yet been identified. Here, we report a putative TREM2 ligand which is secreted from MC38 cells and identified as a cyclophilin A (CypA). A specific interaction between CypA and TREM2 was shown at both protein and cellular levels. Exogenous CypA specifically interacted and co‐localized with TREM2 in RAW264.7 cells, and the physical interactions were shown to regulate TREM2 signaling transduction. The Pro 144 residue in the extracellular domain of TREM2 was found to be the specific binding site of CypA. When considered together, this provides evidence that CypA interacts specifically with TREM2 as a potent ligand.
Title: Cyclophilin A is an endogenous ligand for the triggering receptor expressed on myeloid cells‐2 (TREM2)
Description:
Abstract Triggering receptor expressed on myeloid cells 2 (TREM2) is a cell surface receptor expressed on macrophages, microglial cells, and pre‐osteoclasts, and that participates in diverse cellular function, including inflammation, bone homeostasis, neurological development, and coagulation.
In spite of the indispensable role of the TREM2 protein in the maintenance of immune homeostasis and osteoclast differentiation, the exact ligand for TREM2 has not yet been identified.
Here, we report a putative TREM2 ligand which is secreted from MC38 cells and identified as a cyclophilin A (CypA).
A specific interaction between CypA and TREM2 was shown at both protein and cellular levels.
Exogenous CypA specifically interacted and co‐localized with TREM2 in RAW264.
7 cells, and the physical interactions were shown to regulate TREM2 signaling transduction.
The Pro 144 residue in the extracellular domain of TREM2 was found to be the specific binding site of CypA.
When considered together, this provides evidence that CypA interacts specifically with TREM2 as a potent ligand.

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