Recombinant Mouse Bone morphogenetic protein 6 (Bmp6)

1. These data suggest that, in Hjv(-/-) females, Bmp6 can provide a signal adequate to maintain hepcidin to a level sufficient to avoid extrahepatic iron loading. PMID: 29021231
2. The data demonstrate that endothelial cells are the predominant source of BMP6 in the liver and support a model in which endothelial cells BMP6 has paracrine actions on hepatocyte hemojuvelin to regulate hepcidin transcription and maintain systemic iron homeostasis. PMID: 27864295
3. In summary, our data suggest that in obstructive nephropathy atrophy increases and fibrosis decreases with age and that this relates to increased BMP signaling, most likely due to higher BMP6 and lower CTGF expression. PMID: 27558559
4. In Bmp6-/- mice, iron activated endogenous compensatory mechanisms of other BMPs that were not sufficient for preventing hemochromatosis and bone loss. PMID: 25300398
5. BMP6 expression levels may have potential as predictive markers for the progression of non-alcoholic liver disease. PMID: 25011936
6. The expression of BMP6 in periodontal ligaments may contribute to interaction between the tooth and bone during the eruption and anchoring process. PMID: 25084210
7. BMP-6 secreted by prostate cancer cells induces IL-6 expression in macrophages; IL-6, in turn, stimulates the neuroendocrine differentiation of prostate cancer cells. PMID: 21374653
8. these data highlight a therapeutically innovative role for BMP6 by providing a means to enhance the amount of myogenic lineage derived brown fat. PMID: 24658703
9. These results are consistent with novel mechanisms for regulating Bmp6 and Hamp1 expression. PMID: 24454764
10. Prostate cancer-derived BMP-6 stimulates tumor-associated macrophages to produce IL-1a through a crosstalk between Smad1 and NF-kB1; IL-1a, in turn, promotes angiogenesis and prostate cancer growth. PMID: 24185914
11. In addition to identifying BMP-6 expression in association with xerostomia and xerophthalmia in primary SS, results suggest that BMP-6-induced exocrine dysfunction in SS is independent of autoantibodies and immune activation associated with the disease. PMID: 23982860
12. BMP-6 maintains epithelial polarity via intracellular signaling from basolaterally localized BMP receptors. PMID: 23675417
13. During ovulation induction BMP-6 plays an important role in improvement of oocyte quality and ovarian response of the aged female, possibly by regulation of ovarian inhibitor of DNA-binding proteins (Ids) and VEGF expression. PMID: 23273273
14. Data indicate that BMP-6 in renal cell carcinoma (RCC) cell lines is protumorigenic and involves IL-10-mediated M2 polarization of tumor-associated macrophages (TAM). PMID: 23633487
15. the difference between bone morphogenetic protein-6 (BMP-6) and BMP-7 in enhancing gonadotropin-releasing hormone (GnRH) induced follicle stimulating hormone-beta transcription may be due to differential effects on GnRH-induced signaling PMID: 21846488
16. Loss of Bmp6 regulates retinal iron homeostasis and is associated with age-related macular degeneration. PMID: 21703414
17. results demonstrate that BMP-6-induced IL-1beta expression in macrophages is mediated via a cross-talk between the Smad and the non-Smad pathways through Smad1 and PU.1 PMID: 21571370
18. Loss of endogenous BMP-6 would aggravate renal injury and fibrosis. PMID: 21356359
19. BMP6 promotes normal fertility in female mice, at least in part, by enabling appropriate responses to luteinizing hormone and normal oocyte quality. PMID: 20702851
20. Bmp6 decreased hepcidin levels; increased hepatic iron; and, importantly, corrected hematologic abnormalities in Tmprss6(-/-) mice PMID: 20940420
21. interleukin-6 expression by bone morphogenetic protein-6 in macrophages requires both SMAD and p38 signaling pathways PMID: 20889504
22. in a diabetic mouse model, smooth muscle progenitor cell levels are increased and SPC TGF-beta/BMP-6 expression is modulated PMID: 20858224
23. the regulation of hepatic BMP6 expression by iron is independent of HJV, and expression of HJV in hepatocytes plays an essential role in hepcidin expression by potentiating the BMP6-mediated signaling PMID: 20363739
24. Epithelial cells of the small intestine are the predominant cellular source of BMP6 upon iron sensing PMID: 19786029
25. BMP-6 restores the bone inductive capacity, microarchitecture, and quality of the skeleton in osteoporotic rats PMID: 16798745
26. These results indicate that the BMP6 are differentially expressed in adult spinal cord and are up-regulated during EAE. PMID: 17722066
27. BMP-6 also plays a physiological role in maintaining growth plate function PMID: 17980691
28. Our data indicate that Myo10 is required to guide endothelial migration toward BMP6 gradients via the regulation of filopodial function and amplification of BMP signals. PMID: 18158328
29. Bmp6, Smad7, Id1, and Atoh8 transcripts are significantly modulated by the dietary iron content PMID: 18539898
30. S1P induces osteoblast precursor recruitment and promotes mature cell survival. Wnt10b and BMP6 also were significantly increased in mature osteoclasts, whereas sclerostin levels decreased during differentiation. PMID: 19075223
31. Mice deficient in Bmp6 develop classical hemochromatosis. PMID: 19252488
32. Bone morphogenetic protein signaling is impaired in an HFE knockout mouse model of hemochromatosis. PMID: 19591830

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KEGG: mmu:12161

STRING: 10090.ENSMUSP00000126999

UniGene: Mm.385759