LCK Antibody

1. The ionic CD3-epsilon -Lck interaction controls the phosphorylation level of the T-cell receptor. PMID:28659468
2. a previously unappreciated role for PLC-gamma1 in the positive regulation of Zap-70 and T-cell receptor tyrosine phosphorylation. Conversely, PLC-gamma1 negatively regulated the phosphorylation of SLP-76-associated proteins, including previously established Lck substrate phosphorylation sites within this complex. PMID:28644030
3. autophosphorylation of the LCK active-site loop is indispensable for its catalytic activity and LCK can stimulate its own activation by adopting a more open conformation, which can be modulated by point mutations, and CD4 and CD8, T-cell coreceptors, can enhance LCK activity PMID:29083415
4. the central biological role of the novel IL-2-R/Lck/PLCgamma/PKCtheta;/alphaPIX/Rac1/PYGM signalling pathway is directly related to the control of fundamental cellular processes such as T cell migration and proliferation. PMID:27519475
5. Possible models of regulation of Lck by Aurora-A during T cell activation are described in the review. PMID:27910998
6. Mutation of the basic clusters in the CD28 cytoplasmic domain reduced the recruitment to the CD28-Lck complex of protein kinase Ctheta; (PKCtheta;), which serves as a key effector kinase in the CD28 signaling pathway. PMID:27460989
7. Data suggest that T cell activation through the TCR complex is accompanied by the de novo activation of T-lymphocyte specific protein tyrosine kinase p56lck (Lck) and that phosphorylation of Tyr(394) plays a role in Lck function that goes beyond inducing an open conformation of the kinase. PMID:28096507
8. WASH has a pivotal role for regulation of NK cell cytotoxicity through Lck-mediated Y141 tyrosine phosphorylation. PMID:27441653
9. A phosphosite within the SH2 Domain of Lck regulates its activation by CD45. A negative feedback loop that responds to signaling events tunes active Lck amounts and TCR sensitivity. PMID:28735895
10. The results have revealed a novel splicing homozygous mutation of LCK that may be responsible for the clinical phenotype of HPV infection from latency to invasive carcinoma. PMID:27087313
11. this study show that Lck as a major signaling hub of CD147 in T cells PMID:28148733
12. data indicate that HSP65 suppresses cholesterol efflux and increases cellular cholesterol content through an Lck-mediated pathway in T cells PMID:27742830
13. LSKlow cells, which are derived from LSK cells in p18(-/-) mice, possess lymphoid differentiation ability and short-term repopulation capability. PMID:27287689
14. These results suggest that PM lipids, including phosphatidylinositol 4,5-bisphosphate and phosphatidylinositol 3,4,5-trisphosphate, modulate interaction of Lck with its binding partners in the TCR signaling complex and its TCR signaling activities in a spatiotemporally specific manner via its SH2 domain. PMID:27334919
15. this study shows that p56(lck), which is essential for activation of T cells through the T-cell receptor, is also critical for signal transduction through Toll-like receptors in T cells PMID:26888964
16. Aurora A inhibition causes delocalized clustering of Lck at the immunological synapses and decreases its phosphorylation levels thus indicating Aurora A is required for maintaining Lck active during T-cell activation. PMID:27091106
17. Results demonstrate that Lck represses oxidative phosphorylation through competitive binding with mitochondrial CRIF1 in a kinase-independent manner. PMID:26210498
18. introducing bulky side-chains into this patch (GGxxG to GVxxL) impairs the Lck-independent role of CD4 in T cell activation upon TCR engagement of agonist and weak agonist stimulation. PMID:26147390
19. our results support a novel function of nuclear Lck in promoting human leukemic T cell survival through interaction with a tumor suppressor, CRIF1 PMID:25997448
20. TSAD binds to and co-localizes with Nck. Expression of TSAD increases both Nck-Lck and Nck-SLP-76 interaction in T cells. PMID:26163016
21. These findings demonstrate highly dynamic Lck palmitoylation kinetics that are essential for signaling downstream of the Fas receptor. PMID:26351666
22. Cells from PAX5 translocated patients show LCK up-regulation and over-activation, as well as STAT5 hyper-phosphorylation, compared to PAX5 wt and PAX5 deleted cases. PMID:25595912
23. T cell receptor (TCR)-CD3 complex and the Lck kinase were required for Ca(2+) mobilization but not for apoptosis induction in Jurkat cells. PMID:25947381
24. In T-cells, cholesterol-dependent domains function in the regulation of the Src family kinase Lck (p56lck) by sequestering Lck from its activator CD45. (Review) PMID:25658353
25. Phosphatase CD45 both positively and negatively regulates T cell receptor phosphorylation in reconstituted membrane protein clusters, depending on LCK activity. PMID:25128530
26. Lck is retained in the cytosol of CD222-deficient cells, which obstructs the recruitment of Lck to CD45 at the cell surface, resulting in an abundant inhibitory phosphorylation signature on Lck at the steady state. PMID:25127865
27. Lck mediates signal transmission from CD59 to the TCR/CD3 pathway in Jurkat T cells. PMID:24454946
28. NUP214-ABL1-mediated cell proliferation in T-cell acute lymphoblastic leukemia is dependent on the LCK kinase and various interacting proteins. PMID:23872305
29. LCK phosphorylated Tyr-342 of FOXP3 by immunoprecipitation and in vitro kinase assay, and the replacement of Tyr-342 with phenylalanine (Y342F) abolished the ability to suppress MMP9 expression. PMID:24155921
30. our data reveal how SAP nucleates a previously unknown signaling complex involving NTB-A and LCK to potentiate restimulation-induced cell death of activated human T cells. PMID:24688028
31. Data show a major role for LCK in proximal and distal BCR-mediated signaling in CLL cells and suggest that LCK expression is important in the pathogenesis of CLL. PMID:23505068
32. Nef thus interferes with a specialized membrane microdomain-associated pathway for plasma membrane delivery of newly synthesized Lck whose specificity is determined by the affinity of cargo for these sorting platforms. PMID:23601552
33. In the absence of FAK, the inhibitory phosphorylation of Lck is impaired. PMID:24227778
34. spatial regulation of Lck by CD45 and GM1 ganglioside determines the outcome of apoptotic response to Gal-1 and this local regulation may occur only upon intimate effector (Gal-1 expressing) cell-T-cell attachment. PMID:24231767
35. VP11/12 SFK-binding motifs recruit Lck and the activated Src family kinase then leads (directly or indirectly) to phosphorylation of additional motifs involved in recruiting p85, Grb2, and Shc. PMID:23946459
36. LCK (lymphocyte-specific protein tyrosine kinase) plays a crucial role in T-cell response by transducing early activation signals triggered by TCR (T-cell receptor) engagement. [REVIEW] PMID:23931554
37. conformational states regulate clustering in early T cell signaling PMID:23202272
38. T-cell receptor-induced stimulation of T cells led to simultaneous phosphorylation of p56(lck) residues. PMID:22674786
39. LCK-positive tumour infiltrate is associated with a significantly longer overall survival and time to relapse in patients with radically resected stage I NSCLC. PMID:22457183
40. Data show that cytoskeletal modulation of lipid interactions regulates Lck kinase activity. PMID:22613726
41. increases in Ca(2+) lead to CaMKII activation and subsequent Lck-dependent p66Shc phosphorylation on Serine 36. This event causes both mitochondrial dysfunction and impaired Ca(2+) homeostasis, which synergize in promoting Jurkat T-cell apoptosis. PMID:21983898
42. The Kv1.3/Dlg1/Lck complex is part of the membrane pathway utilized by cyclic AMP to regulate T-cell function. PMID:22378744
43. DHHC2 localizes primarily to the endoplasmic reticulum and Golgi apparatus suggesting that it is involved in S-acylation of newly-synthesized or recycling Lck involved in T cell signalling. PMID:22034844
44. the segment comprising residues 112-126 of human LAT is required for its interaction with Lck. PMID:22034845
45. Feedback circuits monitor and adjust basal Lck-dependent events in T cell receptor signaling. PMID:21917715
46. These results showed that MG132-induced apoptosis was caused by ER stress and subsequent activation of mitochondria-dependent caspase cascade; the presence of p56(lck) enhances MG132-induced apoptosis by augmenting ER stress-mediated apoptotic events. PMID:21819973
47. Data show that MAL regulates membrane order and the distribution of microtubule and transport vesicle docking machinery at the IS and, by doing so, ensures correct protein sorting of Lck and LAT to the cSMAC. PMID:21508261
48. Deregulations of Lck-ZAP-70-Cbl-b cross-talk and miR181a in T cells were found to be associated with cholesterol-dependent-dismantling of HLA-DR rafts in macrophages in leprosy progression. PMID:21453975
49. Preactivated Lck is both necessary and sufficient for T cell activation but remains uncoupled from the T cell receptor in the absence of antigen. PMID:21266711
50. Suppressor of cytokine signaling 1 interacts with oncogenic lymphocyte-specific protein tyrosine kinase. PMID:21234523

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HGNC: 6524

UNIGENE: Hs.470627

KEGG: hsa:3932

STRING: 9606.ENSP00000337825

OMIM: 153390