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. Author manuscript; available in PMC: 2018 Jun 2.
Published in final edited form as: J Mol Biol. 2017 Apr 19;429(11):1607–1629. doi: 10.1016/j.jmb.2017.04.004

Table 2.

Reported TREM2 ligands

Ligand Techniques Variants Ref
Bacteria/bacterial components
Whole Bacteria CS, P, FC, RC, CB, E [75, 121, 122]
C. jejuni lysate E, RC [123]
N. gonococcus lipooligosaccharides E, SPR, RC [124]
Anionic Bacterial Carbohydrates CB [121]
Cholera toxin B E, RC [156]
Mammalian Cells
THP-1 monocytes FC [26]
BMDMs FC [98]
BMDCs FC [100]
Astrocytes RC, CS [121, 125, 126]
Neuronal Cells CS, RC, FC [26, 37, 39, 125]
Apoptotic cells FC, RC, P [30, 37]
Anionic molecules
Phospholipids & Sulfolipids E, DB, RC, LB R47H, R62H ↓ D87N, T96K ↑ [26, 30, 65, 127, 128, 132, 157]
DNA IP, RC [39]
Sulfated proteoglycans FC [26]
Mammalian proteins
HSP60 E, CS. [125]
Plexin-A1 FRET, IP [113]
TREML1 (short transcript) IP [96]
Apolipoproteins (A,B,E,J) DB, P, IP, E, BLI, PM R47H ↓[128, 134] R47H, R62H, D87N↓[135] [128, 134, 135]
Lipoparticles BLI, RC, PM R47H, R62H ↓ D87N↑↓, T96K ↑ [132, 135]
Negative results
Certain Mammalian Cells CS [121]
Apoptotic Jurkat cells FC [128]

Key: E = ELISA, RC = reporter cell, FC = flow cytometry P = phagocytosis/cellular uptake, IP = Co-immunoprecipitation, CB = competitive binding, CS = cell staining, DB = dot blot, LB = liposome binding, BLI = biolayer interferometry, PM = protein microarray, SPR = surface plasmon resonance.