Recombinant Mouse Complement C3 (C3), partial

1. It has been shown that key proteins in the lectin arm of this pathway, MASP1, MASP2 and C3, are expressed in the developing cortex and that neuronal migration is impaired in knockout and knockdown mice. PMID:28462915
2. Complement C3 role in the lung cancer progression. PMID:29118090
3. Data report C3 as a novel myogenic factor secreted by undifferentiated preadipocyte that enhances myogenic differentiation of fetal progenitor cells and adult cells. The results show that complement C3 molecule internalizes myogenic and adipogenic precursor cells and then promotes their differentiation. PMID:28279023
4. C3 deficiency can prolong MHC-II molecule mismatched skin allograft survival. PMID:27641978
5. C3 role in the retinal epithelium and photoreceptor degeneration PMID:28348233
6. These findings shed light on mechanisms of age-related retinal alterations by identifying C3 as a potential therapeutic target for retinal aging. PMID:28928904
7. These findings suggest that C3 protects from early glaucomatous damage, a process that may involve EGFR signaling and other immune responses in the optic nerve head. PMID:28446616
8. complement C3 or downstream complement activation fragments may play an important role in Abeta plaque pathology. PMID:28566429
9. C5 and C5aR have critical roles in the development of C3 glomerulopathy. PMID:28139294
10. Data show that months after irradiation (IR) complement component 3 (C3-/-) mice made fewer errors than WT mice in a reversal learning test indicating better learning capacity in C3-/- mice after IR. PMID:27029069
11. Study show s the regulation of C3 Activation by the Alternative Complement Pathway in the Mouse Retina PMID:27564415
12. Time-lapse video microscopy established the localization of the complement anaphylatoxin C3a and its receptor on enteric neural crest cells during their migration in the embryonic gut. C3a plays a role in regulating collective and directional cell migration, and in ganglia network organization during enteric nervous system ontogenesis. It regulates cell migration in a N-cadherin-dependent process. PMID:27041467
13. nutrient sensing in the liver is coupled to release of C3 and potentially its metabolic and inflammatory functions. PMID:27735945
14. Retinal C3 was expressed by microglia/macrophages located in the outer retina in AMD eyes. In rodent photo-oxidative damage, C3-expressing microglia/macrophages and complement activation were located in regions of lesion expansion in the outer retina over 2 months PMID:28605809
15. Wild-type C57BL/6 mice with pristane-induced lupus developed a strong IFN signature, which was absent in immunoglobulin-deficient (muMT), C3(-/-) , and CD18(-/-) mice. In vivo phagocytosis of dead cells was impaired in C3-deficient mice. PMID:27274010
16. Study found that cancer-cell-derived C3 activates the C3a receptor in the choroid plexus epithelium to disrupt the blood-cerebrospinal fluid (CSF) barrier. This effect allows plasma components, including amphiregulin, and other mitogens to enter the CSF and promote cancer cell growth. PMID:28283064
17. We induced anti-myeloperoxidase vasculitis in mice and confirmed a role for complement activation by demonstrating protection in C3-deficient mice. PMID:27235854
18. These data indicated that alpha7-nAChR caused the inhibition of ASPinduced activation of p38 kinase and NFkappa B to inhibit the production of MCP1 and keratinocytederived chemokine. PMID:27572255
19. These results suggest that GAS utilizes diverse mechanisms to degrade C3b and thus to protect bacterial cells from the complement response of the host. PMID:26945067
20. This study provideed the evidence that C3a plays a critical role in cerebral endothelial activation and leukocyte recruitment during inflammation in the brain. PMID:26822321
21. Demonstrate that cardiac Sirt1 plays an essential role in caloritc restriction-induced cardioprotection against myocardial I/R injury by suppressing cardiac C3 expression. PMID:26873964
22. The roles of C3, CfB, and C3a receptor in the severity of S. aureus induced septic arthritis are reported. PMID:26787717
23. Study shows that C3a is locally produced by -retinal pigment epithelial cells suggesting a key role in early macular degenerations pathogenesis. PMID:26199322
24. Complement C3 activation occurs following intramuscular islet transplantation, but it does not seem to affect the graft function. PMID:26900812
25. Studied whether increased levels of complement in HD brains contributed to disease progression in the R6/2 mouse model of HD. Found C3 deficiency does not alter HD progression in the R6/2 mouse model. PMID:23097680
26. Identify complement 5a as the major C3 activation product that was involved in macrophage polarization and DOCA-salt-induced vascular injury. PMID:25573852
27. our findings define the mechanism of receptor crosstalk between CR3 and Dectin-1 and demonstrate the importance of their collaboration in host defense against fungal infection. PMID:26132276
28. Carboxypeptidase B2 deficiency reveals that complement C3a limits infection in a murine polymicrobial sepsis model. PMID:25851247
29. Complement component 3 is up-regulated via non-canonical TGF-beta signaling in the retinal pigment epithelium PMID:25802332
30. Data indicate that for all three pathways there was a strong correlation between the amount of Ccomplement C3 (C3) fragments and the reduction in functional complement activity. PMID:25733354
31. Therapeutic efficacy of radiotherapy depends on C3a and C5a. PMID:25888260
32. C3 secreted from mycoplasma-infected Mesenchymal stem cells (MSCs) has an important role in the immunomodulatory functions of MSCs. PMID:24763049
33. Data indicate that absence of complement C3, complement C5 and Fc receptor subunit gamma (FcRgamma) does not impact autoantibody production in K/BxN mice. PMID:23237573
34. These results suggest that osteoclast-derived C3a functions in the relay from bone resorption to formation and may be a candidate for a coupling factor. PMID:24470120
35. Coagulation cascades, by generating thrombin and plasmin, respectively, provide C5 convertase activity, explaining why mobilization of hematopoietic stem cells in C3-deficient mice. PMID:24667943
36. These results provide new insights into the role of systemic C3 in regulating contraction following intracellular bacterial infection and may help to develop vaccines that are more effective. PMID:25187659
37. a role for outside-in iC3b-CD11b signals in limiting intrinsic organ inflammation PMID:24632830
38. have identified Complement C3 as a candidate plasma biomarker for measuring disease state in neuroblastoma PMID:24200836
39. A previously unknown function of C3a promotes protection to both myeloid and lymphoid cells against Listeria monocytogenes-induced apoptosis. PMID:24981453
40. Genetic and intervention studies implicating complement C3 as a major target for the treatment of periodontitis. PMID:24808362
41. Loss of dopaminergic neurons was rescued by complement C3-deficient mice. PMID:24948809
42. Complement protein C3 exacerbates prion disease in a mouse model of chronic wasting disease. PMID:24038599
43. Complement C3 and C5 deficiency affects bone fracture healing. PMID:24260573
44. Radiation combined injury-induced alterations of corticosterone, CRP, C3, IgM, and PGE2 cause homeostatic imbalance and may contribute to reduced survival. PMID:24175013
45. Data indicate that co-deficiency of factor H (FH) and MASP-1/MASP-3 did not ameliorate either the plasma Complement C3 (C3) activation or glomerular C3 accumulation in FH-deficient mice. PMID:24279761
46. The results of this study suggested that C3 plays a role in the regulation of the number and function of glutamatergic synapses in the hippocampus and exerts negative effects on hippocampus-dependent cognitive performance. PMID:24378428
47. C3 induces epithelial-to-mesenchymal transition and may be a primary factor to activate the renal renin-angiotensin systems to induce hypertension. PMID:23926185
48. Data indicate complement C3 deposition on peanut extract (PE) was abolished in immunoglobulin- and C4-deficient sera. PMID:23182714
49. ALI in H5N1-infected mice was caused by excessive complement activation, as demonstrated by deposition of C3, C5b-9, and MBL-C in lung tissue, and by up-regulation of MBL-associated serine protease-2 and the complement receptors C3aR and C5aR. PMID:23526211
50. in vitro results suggest various metabolic hormones and inflammatory factors can affect acylation stimulating protein (ASP) production and that ASP could constitute a new link between adipocytes and macrophage PMID:23430572

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UNIGENE: Mm.19131

KEGG: mmu:12266

STRING: 10090.ENSMUSP00000024988