Signaling Lymphocytic Activation Molecule Family Member 1 Proteine (SLAMF1)

Mouse (Murine) Signaling Lymphocytic Activation Molecule Family Member 1 (SLAMF1) Interaktionspartner

1. the Slam locus has an overall inhibitory role during NK cell activation that is solely dependent on 2B4. This effect is influenced by cytokines and leads to suppression of LFA-1 activity.

2. CRISPR-Mediated Slamf1Delta/Delta Slamf5Delta/Delta Slamf6Delta/Delta Triple Gene Disruption Reveals NKT Cell Defects but Not T Follicular Helper Cell Defects.

3. We demonstrated that Bacille Calmette-Guerin infection significantly upregulated SLAMF1, which enhanced inflammatory response by activating the NF-kappaB signaling pathway and facilitated bacterial clearance in BCG-infected RAW264.7 cells and mice.

4. Slamf1 and Slamf8 govern ROS-dependent innate immune responses of myeloid cells.

5. The combined effects of RIIB deletion and pathogenic SLAM can lead to severe lupus nephritis in the B6 genetic background.

6. SLAM-SAP signaling promotes differentiation of IL-17-producing T cells and progression of experimental autoimmune encephalomyelitis.

7. The goal of the current study was to determine whether Slam haplotype affected NKT and Vgamma4+ T-cell responses subsequent to coxsackievirus b3 infection.

8. Signaling lymphocyte activation molecule regulates development of colitis in mice.

9. Slamf1, which controls phagosomal/lysosomal fusion and phagosomal NADPH-oxidase activity, is required for T.cruzi replication in macrophages and dendritic cells, but not in other cells, which do not express the receptor.

10. conclude that Slamf1 recruits a subset of Vps34-associated proteins, which is involved in membrane fusion and NOX2 regulation

11. Slamf1 is a bacterial sensor that regulates intracellular enzyme activities involved in the removal of Gram-negative bacteria.

12. SLAM signaling drives most of (interleukin) IL-4 production by germinal center T follicular helper CD4 cells.

13. Polymorphisms that distinguish two Slam haplotypes significantly modulate the innate immune response in vivo through their effect on natural killer T (NKT) cells.

14. role of SAP in murine antigen-mediated T-cell proliferation and interferon gamma production

15. Coreceptor SLAM plays a central role at the interface of acquired and innate immune responses.

16. Cell surface receptors of the SLAM family, including CD150, CD244, and CD48, were differentially expressed among functionally distinct hematopoietic progenitor cells.

17. SLAM/SLAM interactions inhibit CD40-induced signal transduction in monocyte-derived dendritic cells.

18. Data show that the interaction of the FynT SH3 domain with SLAM-SAP is strictly inducible, and is dependent on engagement of SLAM by extracellular ligands.

19. control of NKT cell numbers attributed to the Nkt1 gene is mediated by differential expression of Slamf1 and an additional contribution by Slamf6.

20. Both CD150(+) and CD150(-) cells can be found within the stem cell population population and both populations can contribute to long-term multilineage reconstitution.

Human Signaling Lymphocytic Activation Molecule Family Member 1 (SLAMF1) Interaktionspartner

1. CD150 and CD180 receptors may modulate transcriptional program in lymphocytic leukemia cells by regulating the transcription factor expression levels

2. this paper shows that the X-linked lymphoproliferative disease gene product SAP regulates signals induced through the co-receptor SLAM

3. combination of signals via CD150 and CD180 leads to blocking of pro-survival pathways that may be a restraining factor for neoplastic CLL B cells propagation in more than 50% of CLL cases where these receptors are coexpressed

4. EBF1 is critical for transcriptional control of SLAMF1 gene in human B cells.

5. MeV can hijack SLAMF1 to drive endocytosis using a complex pathway that shares features with canonical viral macropinocytosis, phagocytosis, and mechanotransduction. This uptake pathway is specific to SLAMF1-positive cells and occurs within 60 min of viral attachment.

6. Malignant B-cell lines at the different stages of maturation only partially resemble their normal counterparts by CD150 expression. In malignant B-cell lines, CD150 expression on mRNA level is much broader than on protein level. CD150 isoforms are differentially expressed in normal and malignant B cells with predominant expression of mCD150 isoform.

7. Data suggest that SLAMF1 is another significant piece in the intricate defective immune-regulatory function of patients with SLE.

8. results indicate that loss of SLAMF1 expression in chronic lymphocytic leukemia modulates genetic pathways

9. Upstream open reading frames regulate translation of the long isoform of SLAMF1 mRNA that encodes costimulatory receptor CD150

10. Molecular dynamics analysis revealed that mutant R32Q and T53I structures of SAP exhibited structural variation with respect to their backbone atoms before and after binding with the unphosphorylated SLAM peptide.

11. Signaling lymphocytic activation molecule (SLAM)/SLAM-associated protein pathway regulates human B-cell tolerance.

12. Latent membrane protein 1 was responsible for the CD150 upregulation.

13. Experimental adaptation of wild-type canine distemper virus (CDV) to the human entry receptor CD150

14. Two genes were consistently retained in the models with clinical variables: SKI (v-SKI avian sarcoma viral oncogene homolog) and SLAMF1 (signaling lymphocytic activation molecule family member 1; CD150).

15. conclude that Slamf1 recruits a subset of Vps34-associated proteins, which is involved in membrane fusion and NOX2 regulation

16. HIV-1 infection induces a high level of SLAM expression on CD4(+) T cells, which may enhance their susceptibility to measles virus and exacerbate measles in coinfected individuals.

17. the study demonstrates that variants of SLAMF1 and ITLN1, both implicated in inflammation, are associated with type 2 diabetes in Indians.

18. Subjects previously immunized with measles-mumps-rubella vaccine were genotyped for 66 candidate single nucleotide polymorphisms in the CD46, SLAM and CD209 genes.

19. The simultaneous interaction of Measles virus glycoprotein-pseudotyped Lentivirus with both CD46 and SLAM is required to achieve efficient and stable transduction of B and T cells.

20. CD150 receptor could trigger PI3K-mediated Akt signaling pathway in normal, EBV-transformed and malignant B cells.