| 2018 |
VSIG-3/IGSF11 binds specifically to the B7 family member VISTA (PD-1H) as determined by functional ELISA binding screening; this interaction inhibits human T-cell proliferation and reduces cytokine/chemokine production (IFN-γ, IL-2, IL-17, CCL5, CCL3, CXCL11). Anti-VISTA neutralizing antibodies attenuate both VSIG-3/VISTA binding and VSIG-3-induced T-cell inhibition. |
Functional ELISA binding assay, T-cell proliferation assay, cytokine production assay, neutralizing antibody blocking experiment |
Immunology |
High |
30220083
|
| 2021 |
Crystal structure of the extracellular domain (ECD) of human VSIG3/IGSF11 was solved at 2.64 Å resolution; interaction of VSIG3 with VISTA was validated by co-immunoprecipitation. A small molecule inhibitor (K284-3046) of VSIG3 was identified based on protein-protein docking. |
X-ray crystallography (2.64 Å), co-immunoprecipitation, protein-protein docking, in vitro inhibitor evaluation |
Frontiers in immunology |
High |
33841409
|
| 2015 |
IgSF11 is a dual-binding partner of PSD-95 (postsynaptic scaffolding protein) and AMPA glutamate receptors (AMPARs) at excitatory synapses. IgSF11 requires PSD-95 binding for its excitatory synaptic localization. IgSF11 stabilizes synaptic AMPARs: knockdown suppresses AMPAR-mediated synaptic transmission and increases surface mobility of AMPARs (single-molecule tracking). IgSF11 deletion in mice suppresses AMPAR-mediated synaptic transmission in dentate gyrus and LTP in CA1 hippocampus. |
Co-immunoprecipitation, single-molecule tracking (high-throughput), IgSF11 KD (knockdown), IgSF11 KO mouse electrophysiology (AMPAR-mediated currents, LTP recording) |
Nature neuroscience |
High |
26595655
|
| 2005 |
BT-IgSF/IGSF11 functions as a cell adhesion molecule mediating homophilic, Ca2+/Mg2+-independent cell aggregation. The cytoplasmic tail is not required for adhesion function, and β1 integrin is not involved. |
Overexpression in TF-1-fms and NIH/3T3 cells, cell aggregation assay, neutralizing antibody (anti-β1 integrin), flow cytometric analysis, inducible expression system |
Journal of cellular physiology |
High |
15795899
|
| 2012 |
Igsf11 (zebrafish ortholog) mediates adhesive interactions and is required cell-autonomously in the melanophore lineage for adult stripe development; igsf11 mutants show defects in melanophore migration and survival, as demonstrated by cell transplantation and genetic rescue experiments. |
Forward genetic screen (seurat mutant), cell transplantation, genetic rescue, in vitro/in vivo/ex vivo cell behavior analyses |
PLoS genetics |
High |
22916035
|
| 2020 |
IgSF11 regulates osteoclast differentiation and bone resorption through interaction with PSD-95 scaffold protein. IgSF11 functions through homophilic interactions during osteoclast differentiation. The IgSF11–PSD-95 interaction requires the 75 C-terminal amino acids of IgSF11. IgSF11-deficient mice show impaired osteoclast differentiation and bone resorption but no bone formation defect, resulting in increased bone mass. |
IgSF11 KO mouse model, in vitro osteoclast culture, domain deletion rescue experiments, bone histomorphometry |
Bone research |
High |
32047704
|
| 2023 |
IgSF11 controls osteoclast differentiation by regulating pyruvate kinase M2 (PKM2) activity. IgSF11 activates Src family kinases (c-Src, Fyn, HcK), which phosphorylate PKM2 on tyrosine residues, inhibiting PKM2 activity. IgSF11-deficient cells show higher PKM2 activity and defective osteoclast differentiation. Pharmacological inhibition of PKM2 (Shikonin) rescues differentiation in IgSF11-KO cells; PKM2 activation (TEPP46) suppresses wild-type osteoclast differentiation. |
Controlled IgSF11 activation system, phosphoproteomics (PKM2 identification), kinase activity assays, pharmacological rescue (Shikonin, TEPP46), IgSF11-KO cells, in vivo bone resorption assay |
Bone research |
High |
36928396
|
| 2017 |
BT-IgSF/IgSF11 is localized in Sertoli cells at the blood-testis barrier (BTB) and apical ectoplasmic specialization. Conditional KO (AMHCre, Rosa26CreERT2) in Sertoli cells causes male infertility, azoospermia, and spermatogenesis arrest. BTB functional integrity is impaired (BTB-impermeable tracer assay) despite normal BTB ultrastructure. Absence of BT-IgSF leads to mislocalization of connexin43 throughout the seminiferous epithelium rather than being restricted to the BTB, suggesting impaired cell-cell communication. |
Global and conditional KO mouse models, BTB tracer injection (in vivo permeability assay), immunofluorescence localization, electron microscopy, RT-qPCR |
The Journal of biological chemistry |
High |
29123028
|
| 2021 |
IGSF11 deficiency in mice leads to failure of pericentric heterochromatin dissociation during meiotic diplotene; spermatocytes accumulate interchromosomal interactions (detected by Hi-C) mostly at chromosome ends. IGSF11 is required in both Sertoli (somatic) cells and spermatogenic cells for primary spermatocyte development, demonstrated by testicular cell transplantation. |
IGSF11 KO mouse, meiotic fluorescent reporter system, testicular cell transplantation, Hi-C chromosome conformation capture |
PLoS genetics |
High |
34491997
|
| 2021 |
IgSF11 homophilic adhesion proteins are preferentially expressed in chandelier cells (ChCs) and their postsynaptic target layer in the neocortex. Loss-of-function in either ChCs or postsynaptic pyramidal neurons impairs layer-specific ChC synaptic development. Overexpression of IgSF11 in ChCs enlarges presynaptic boutons; expressing IgSF11 in non-target layers induces ectopic ChC synapses, demonstrating that IgSF11 homophilic interactions determine layer-specific synaptic connectivity. |
IgSF11 KO, conditional loss-of-function in ChCs or postsynaptic cells, overexpression in ChCs and non-target layers, synaptic morphology analysis (imaging) |
Science advances |
High |
34261648
|
| 2024 |
BT-IgSF/IgSF11 KO in mice causes increased clustering and reduced protein levels of connexin43 (Gja1) in astrocytes and ependymal cells, and decreased astrocyte-astrocyte gap junction coupling (biocytin spread assay in hippocampal/cortical slices). The lysosomal pathway mediates increased connexin43 degradation in the absence of BT-IgSF. Connexin30 (Gjb6) and neuronal connexin36 (Gjd2) are not affected. |
BT-IgSF global KO mouse, biocytin coupling assay in acute brain slices, protein biosynthesis/proteolysis inhibition experiments, immunofluorescence for connexin localization |
eNeuro |
High |
38388443
|
| 2020 |
CD44 can compensate for IgSF11 deficiency in osteoclast differentiation by associating with PSD-95. Antibody-mediated CD44 stimulation or low-molecular-weight hyaluronan (LMW-HA) treatment rescues impaired osteoclast differentiation in IgSF11-KO cultures. PSD-95 knockdown abrogates these rescue effects, demonstrating that both IgSF11 and CD44 act through PSD-95. |
IgSF11 KO osteoclast cultures, antibody-mediated CD44 stimulation, LMW-HA treatment, RNAi knockdown of PSD-95, biochemical Co-IP analysis |
International journal of molecular sciences |
Medium |
32290171
|
| 2018 |
BT-IgSF/IgSF11 suppresses proliferation and promotes differentiation of cerebellar granule cell precursors (CGCPs). BT-IgSF is expressed in the molecular layer where CGCPs are in the differentiation stage. Knockdown reduces differentiation; overexpression promotes differentiation into cerebellar granule cells. |
BT-IgSF KD and overexpression in primary cultured CGCPs, proliferation and differentiation assays, expression analysis in developing cerebellum |
Neuroscience letters |
Medium |
30176341
|
| 2005 |
IGSF11 siRNA knockdown retards the growth of gastric cancer cells. |
siRNA knockdown, cell growth assay |
Cancer science |
Low |
16108831
|
| 2025 |
IgSF11 forms a complex with RAS-associated protein 1 (RAP1), identified by immunoprecipitation-mass spectrometry. The L372-R378 region of IgSF11 is required for recruiting RAP1 and driving melanoma cell migration and invasion. IgSF11-expressing melanoma cells show enrichment of EMT gene signatures. |
Immunoprecipitation-mass spectrometry, IgSF11 KO and re-expression cell lines, domain deletion mutants, migration/invasion assays in vitro and in vivo |
Cell communication and signaling |
Medium |
40635001
|
| 2023 |
miR-125a-5p represses IGSF11/VSIG3 expression, and adenosine methylation (m6A) of miR-125a-5p by METTL3 (read by KHDRBS3 and HuR) relieves this repression, leading to IGSF11 overexpression and immune escape in lung cancer. Anti-PD-1 therapy saturation of PD-1 induces this cascade. VSIG3/IGSF11 protein-protein interaction (with VISTA) was confirmed by Co-IP in this context. |
CLIP, oligonucleotide pulldown, Co-IP, qPCR, MemiRIP (m6A-RIP), cell-based assays |
Cancers |
Medium |
37370798
|
| 2025 |
IGSF11/VISTA immune checkpoint axis is functionally operative in diffuse midline glioma (DMG); IGSF11 is primarily expressed by AOO-associated cancer cells while VISTA is detected in homeostatic microglia. Targeting IGSF11-VISTA results in tumor reduction and survival benefit mediated by brain-resident microglia and independent of T cell infiltration. |
Single-nuclei RNA sequencing, spatial transcriptomics, high-dimensional imaging, murine DMG model with IGSF11-VISTA targeting |
Cancer cell |
Medium |
41576930
|