Recombinant Mouse Junctional adhesion molecule A (F11r)

1. Deletion JAM-A from platelets increases early-stage neointima formation after carotid artery wire injury in hyperlipidemic mice. PMID:28211187
2. JAM-A is present in the prostate and seminal vesicles and in all three regions of the epididymis where it is secreted in epididymosomes in the luminal fluid and can be delivered to sperm. PMID:28062807
3. Soluble JAM-A secreted from cardiac progenitor cells reduces infiltration of neutrophils after myocardial infarction and ameliorates tissue damage through prevention of excess inflammation. PMID:25468657
4. JAM-A up-regulation can increase the proliferation, cytokine secretion and wound-homing ability of MSCs, thus accelerating the repair rate of full-thickness skin defects PMID:25994236
5. Endothelial JAM-A but not hematopoietic JAM-A facilitates reovirus T1L bloodstream entry and egress. PMID:25149763
6. Deletion of JAM-A causes a gain-of-function in platelets, with lower activation thresholds and increased inflammatory activities. This leads to an increase of plaque formation, particularly in early stages of the disease. PMID:25472975
7. The F11r gene is directly regulated by retinoic acid in the embryonic mesoderm. PMID:25251699
8. Redistribution of JAM-A in endothelial cells after stimulation with pro-atherogenic oxidized lipoproteins results in increased transmigration of mononuclear cells. PMID:24704627
9. JAM-A has a prominent role in regulating leukocyte infiltration after brain I/R injury and could be a new target in limiting post-ischemic inflammation. PMID:24657919
10. JAM-A regulates epithelial permeability via association with ZO-2, afadin, and PDZ-GEF1 to activate Rap2c and control contraction of the apical cytoskeleton. PMID:23885123
11. Cancer stem cells selectively express JAM-A, which regulates self-renewal. PMID:24373972
12. These studies establish F11R as a novel monocyte prognostic marker for GBM critical for defining a subpopulation of stromal cells for future potential therapeutic intervention. PMID:24147027
13. Our data identify endothelial JAM-A as an important effector molecule integrating atherogenic conditions to direct inflammatory cell entry at predilection sites of atherosclerosis. PMID:24065611
14. The JAM-A and ZO-1 genes were highly expressed in all the tested tissues. PMID:23568966
15. Junctional adhesion molecule-A regulates vascular endothelial growth factor receptor-2 signaling-dependent mouse corneal wound healing. PMID:23667656
16. The crucial role of JAM-A in the transmigration of neutrophils from the vasculature into inflamed tissues. PMID:22904169
17. The chemokine (C-C motif) ligand 2 (CCL2) induced JAM-A redistribution from the interendothelial cell area to the apical surface of brain endothelial cells. PMID:22733993
18. CASK negatively regulates PMCA4b by directly binding to it and JAM-A positively regulates it indirectly through CASK PMID:22020416
19. JAM-A normally limits platelet accumulation by inhibiting integrin outside-in signaling thus preventing premature platelet activation. PMID:22271446
20. Data suggest that aPKC phosphorylates JAM-A at S285 to regulate cell-cell contact maturation, TJ formation, and single lumen specification. PMID:22371556
21. downregulation of JAM-A reduces tumor aggressive behavior by increasing cell susceptibility to apoptosis PMID:21695058
22. Data demenstrate that JAM-A restricts intestinal epithelial cell (IEC) proliferation in a dimerization-dependent manner, by inhibiting Akt-dependent beta-catenin activation. PMID:21372850
23. Our data show that JAM-A is a novel surface marker for NG2-glia cells of the adult brain. PMID:20184779
24. In the Rip1Tag2 tumor model, abrogation of JAM-A reduces cancer development by increasing antitumor immune response. PMID:20160037
25. JAM-1 did not contribute to global embryo compaction and adhesion but rather regulated the timing of blastocoel cavity formation dependent upon establishment of the trophectoderm tight junction paracellular seal. PMID:15494378
26. By regulating cytoskeletal and adhesive structures, JAM-A expression prevents cell motility, probably in a PSD95-Dlg-ZO1-dependent manner. PMID:15657074
27. JAM-A is up-regulated in hepatic venules and serves as an endothelial receptor of neutrophil transmigration, but it does not mediate leukocyte rolling, adhesion, or platelet-endothelial cell interactions. PMID:15827135
28. JAM-A is required for the correct infiltration of polymorphonuclear leukocytes into an inflamed peritoneum or in the heart upon ischemia-reperfusion injury. PMID:16027360
29. crucial role of JAM-A in accelerated lesion formation and monocyte infiltration in atherosclerosis-prone mice PMID:16306427
30. Taken together, these data indicate that JAM-A regulates cell motility by cooperating with microtubule-stabilizing pathways. PMID:16783819
31. Essential role for JAM-A in FGF-2-induced angiogenesis. PMID:16809549
32. JAM-A is expressed in the corneal epithelium where it appears to regulate cell shape. PMID:17118692
33. Junctional adhesion molecule-A is critical for the formation of pseudocanaliculi and modulates E-cadherin expression in hepatic cells PMID:17623668
34. JAM-A is expressed on hematopoietic precursors in various hematopoietic tissues PMID:17986666
35. The findings show that JAM-A is involved in sperm tail formation and is essential for normal motility, which may occur via its signal transduction and protein phosphorylation properties. PMID:18022613
36. JAM-A plays a role in intestinal homeostasis by regulating epithelial permeability, inflammation, and proliferation PMID:18039951
37. A short bond lifetime imparts a highly dynamic nature to homophilic JAM-A interactions for regulating tight junction permeability while stable interactions between sigma1 and JAM-A likely anchor the virus to the cell surface and facilitate viral entry. PMID:18446885
38. nonredundant and novel role of JAM-A in controlling mucosal homeostasis by regulating the integrity and permeability of epithelial barrier function PMID:18514073
39. Nectin plays a novel role in the co-localization of JAM and claudin at the same cell-cell adhesion membrane domains. PMID:18547333
40. These data indicate that JAM-A is required for the correct internalization and recycling of integrins during cell migration. PMID:19118219
41. The authors inoculated wild-type (WT) and isogenic JAM-A(-/-) mice perorally with reovirus and found that JAM-A is dispensable for viral replication in the intestine but required for systemic dissemination. PMID:19154988

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UNIGENE: Mm.294882

KEGG: mmu:16456

STRING: 10090.ENSMUSP00000041907