Artigo Acesso aberto Revisado por pares

Histone H4-related osteogenic growth peptide (OGP): a novel circulating stimulator of osteoblastic activity.

1992; Springer Nature; Volume: 11; Issue: 5 Linguagem: Inglês

10.1002/j.1460-2075.1992.tb05238.x

ISSN

1460-2075

Autores

I. Bab, Dan Gazit, M. Chorev, András Mühlrád, A. Shteyer, Zvi Greenberg, Malka Namdar, A. J. Kahn,

Tópico(s)

GDF15 and Related Biomarkers

Resumo

Research Article1 May 1992free access Histone H4-related osteogenic growth peptide (OGP): a novel circulating stimulator of osteoblastic activity. I. Bab I. Bab Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author D. Gazit D. Gazit Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author M. Chorev M. Chorev Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author A. Muhlrad A. Muhlrad Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author A. Shteyer A. Shteyer Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author Z. Greenberg Z. Greenberg Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author M. Namdar M. Namdar Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author A. Kahn A. Kahn Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author I. Bab I. Bab Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author D. Gazit D. Gazit Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author M. Chorev M. Chorev Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author A. Muhlrad A. Muhlrad Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author A. Shteyer A. Shteyer Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author Z. Greenberg Z. Greenberg Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author M. Namdar M. Namdar Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author A. Kahn A. Kahn Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. Search for more papers by this author Author Information I. Bab1, D. Gazit1, M. Chorev1, A. Muhlrad1, A. Shteyer1, Z. Greenberg1, M. Namdar1 and A. Kahn1 1Bone Laboratory, Hebrew University Faculty of Dental Medicine, Jerusalem, Israel. The EMBO Journal (1992)11:1867-1873https://doi.org/10.1002/j.1460-2075.1992.tb05238.x PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info It has been established that regenerating marrow induces an osteogenic response in distant skeletal sites and that this activity is mediated by factors released into the circulation by the healing tissue. In the present study we have characterized one of these factors, a 14 amino acid peptide named osteogenic growth peptide (OGP). Synthetic OGP, identical in structure to the native molecule, stimulates the proliferation and alkaline phosphatase activity of osteoblastic cells in vitro and increases bone mass in rats when injected in vivo. Immunoreactive OGP in high abundance is present physiologically in the serum, mainly in the form of an OGP-OGP binding protein complex. A marked increase in serum bound and unbound OGP accompanies the osteogenic phase of post-ablation marrow regeneration and associated systemic osteogenic response. Authentic OGP is identical to the C-terminus of histone H4 and shares a five residue motif with a T-cell receptor beta-chain V-region and the Bacillus subtilis outB locus. Since these latter proteins have not been implicated previously in the control of cell proliferation or differentiation, OGP may belong to a novel, heretofore unrecognized family of regulatory peptides. Perhaps more importantly, OGP appears to represent a new class of molecules involved in the systemic control of osteoblast proliferation and differentiation. Previous ArticleNext Article Volume 11Issue 51 May 1992In this issue RelatedDetailsLoading ...

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