Preptin, another peptide product of the pancreatic beta-cell, is osteogenic in vitro and in vivo
1 Department of Medicine and 2 School of Biological Sciences, University of Auckland, Auckland, New Zealand Submitted 20 December 2005 ; accepted in final form 7 August 2006 Several hormones that regulate nutritional status also impact on bone metabolism. Preptin is a recently isolated 34-amino acid...
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creator | Cornish, J Callon, K. E Bava, U Watson, M Xu, X Lin, J. M Chan, V. A Grey, A. B Naot, D Buchanan, C. M Cooper, G. J. S Reid, I. R |
description | 1 Department of Medicine and 2 School of Biological Sciences, University of Auckland, Auckland, New Zealand
Submitted 20 December 2005
; accepted in final form 7 August 2006
Several hormones that regulate nutritional status also impact on bone metabolism. Preptin is a recently isolated 34-amino acid peptide hormone that is cosecreted with insulin and amylin from the pancreatic -cells. Preptin corresponds to Asp 69 -Leu 102 of pro-IGF-II. Increased circulating levels of a pro-IGF-II peptide complexed with IGF-binding protein-2 have been implicated in the high bone mass phenotype observed in patients with chronic hepatitis C infection. We have assessed preptin's activities on bone. Preptin dose-dependently stimulated the proliferation (cell number and DNA synthesis) of primary fetal rat osteoblasts and osteoblast-like cell lines at periphysiological concentrations (>10 11 M). In addition, thymidine incorporation was stimulated in murine neonatal calvarial organ culture, likely reflecting the proliferation of cells from the osteoblast lineage. Preptin did not affect bone resorption in this model. Preptin induced phosphorylation of p42/p44 MAP kinases in osteoblastic cells in a dose-dependent manner (10 8 -10 10 M), and its proliferative effects on primary osteoblasts were blocked by MAP kinase kinase inhibitors. Preptin also reduced osteoblast apoptosis induced by serum deprivation, reducing the number of apoptotic cells by >20%. In vivo administration of preptin increased bone area and mineralizing surface in adult mice. These data demonstrate that preptin, which is cosecreted from the pancreatic -cell with amylin and insulin, is anabolic to bone and may contribute to the preservation of bone mass observed in hyperinsulinemic states such as obesity.
osteoblast; bone-active hormone; bone anabolic
Address for reprint requests and other correspondence: J. Cornish, Dept. of Medicine, Univ. of Auckland, Private Bag 92019, Auckland, NZ (e-mail: j.cornish{at}auckland.ac.nz ) |
doi_str_mv | 10.1152/ajpendo.00642.2005 |
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Submitted 20 December 2005
; accepted in final form 7 August 2006
Several hormones that regulate nutritional status also impact on bone metabolism. Preptin is a recently isolated 34-amino acid peptide hormone that is cosecreted with insulin and amylin from the pancreatic -cells. Preptin corresponds to Asp 69 -Leu 102 of pro-IGF-II. Increased circulating levels of a pro-IGF-II peptide complexed with IGF-binding protein-2 have been implicated in the high bone mass phenotype observed in patients with chronic hepatitis C infection. We have assessed preptin's activities on bone. Preptin dose-dependently stimulated the proliferation (cell number and DNA synthesis) of primary fetal rat osteoblasts and osteoblast-like cell lines at periphysiological concentrations (>10 11 M). In addition, thymidine incorporation was stimulated in murine neonatal calvarial organ culture, likely reflecting the proliferation of cells from the osteoblast lineage. Preptin did not affect bone resorption in this model. Preptin induced phosphorylation of p42/p44 MAP kinases in osteoblastic cells in a dose-dependent manner (10 8 -10 10 M), and its proliferative effects on primary osteoblasts were blocked by MAP kinase kinase inhibitors. Preptin also reduced osteoblast apoptosis induced by serum deprivation, reducing the number of apoptotic cells by >20%. In vivo administration of preptin increased bone area and mineralizing surface in adult mice. These data demonstrate that preptin, which is cosecreted from the pancreatic -cell with amylin and insulin, is anabolic to bone and may contribute to the preservation of bone mass observed in hyperinsulinemic states such as obesity.
osteoblast; bone-active hormone; bone anabolic
Address for reprint requests and other correspondence: J. Cornish, Dept. of Medicine, Univ. of Auckland, Private Bag 92019, Auckland, NZ (e-mail: j.cornish{at}auckland.ac.nz )</description><identifier>ISSN: 0193-1849</identifier><identifier>EISSN: 1522-1555</identifier><identifier>DOI: 10.1152/ajpendo.00642.2005</identifier><identifier>PMID: 16912056</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Bone Development - drug effects ; Cell Differentiation - drug effects ; Cell Proliferation - drug effects ; Cell Survival - drug effects ; Cells, Cultured ; Humans ; Insulin-Like Growth Factor II - metabolism ; Insulin-Like Growth Factor II - pharmacology ; Insulin-Secreting Cells - metabolism ; Male ; Mice ; Mitogen-Activated Protein Kinase 1 - metabolism ; Mitogen-Activated Protein Kinase 3 - metabolism ; Osteoblasts - cytology ; Osteoblasts - drug effects ; Osteoclasts - metabolism ; Osteogenesis - drug effects ; Peptide Fragments - metabolism ; Peptide Fragments - pharmacology ; Peptides - metabolism ; Peptides - pharmacology ; Pertussis Toxin - pharmacology ; Rats ; Receptors, Islet Amyloid Polypeptide ; Receptors, Peptide - antagonists & inhibitors ; Swiss 3T3 Cells</subject><ispartof>American journal of physiology: endocrinology and metabolism, 2007-01, Vol.292 (1), p.E117-E122</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-1e4deb0fafc139efe0732ab672a89379db1dcb10ff181a091eb7c11b0febdf913</citedby><cites>FETCH-LOGICAL-c420t-1e4deb0fafc139efe0732ab672a89379db1dcb10ff181a091eb7c11b0febdf913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,3026,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16912056$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cornish, J</creatorcontrib><creatorcontrib>Callon, K. E</creatorcontrib><creatorcontrib>Bava, U</creatorcontrib><creatorcontrib>Watson, M</creatorcontrib><creatorcontrib>Xu, X</creatorcontrib><creatorcontrib>Lin, J. M</creatorcontrib><creatorcontrib>Chan, V. A</creatorcontrib><creatorcontrib>Grey, A. B</creatorcontrib><creatorcontrib>Naot, D</creatorcontrib><creatorcontrib>Buchanan, C. M</creatorcontrib><creatorcontrib>Cooper, G. J. S</creatorcontrib><creatorcontrib>Reid, I. R</creatorcontrib><title>Preptin, another peptide product of the pancreatic beta-cell, is osteogenic in vitro and in vivo</title><title>American journal of physiology: endocrinology and metabolism</title><addtitle>Am J Physiol Endocrinol Metab</addtitle><description>1 Department of Medicine and 2 School of Biological Sciences, University of Auckland, Auckland, New Zealand
Submitted 20 December 2005
; accepted in final form 7 August 2006
Several hormones that regulate nutritional status also impact on bone metabolism. Preptin is a recently isolated 34-amino acid peptide hormone that is cosecreted with insulin and amylin from the pancreatic -cells. Preptin corresponds to Asp 69 -Leu 102 of pro-IGF-II. Increased circulating levels of a pro-IGF-II peptide complexed with IGF-binding protein-2 have been implicated in the high bone mass phenotype observed in patients with chronic hepatitis C infection. We have assessed preptin's activities on bone. Preptin dose-dependently stimulated the proliferation (cell number and DNA synthesis) of primary fetal rat osteoblasts and osteoblast-like cell lines at periphysiological concentrations (>10 11 M). In addition, thymidine incorporation was stimulated in murine neonatal calvarial organ culture, likely reflecting the proliferation of cells from the osteoblast lineage. Preptin did not affect bone resorption in this model. Preptin induced phosphorylation of p42/p44 MAP kinases in osteoblastic cells in a dose-dependent manner (10 8 -10 10 M), and its proliferative effects on primary osteoblasts were blocked by MAP kinase kinase inhibitors. Preptin also reduced osteoblast apoptosis induced by serum deprivation, reducing the number of apoptotic cells by >20%. In vivo administration of preptin increased bone area and mineralizing surface in adult mice. These data demonstrate that preptin, which is cosecreted from the pancreatic -cell with amylin and insulin, is anabolic to bone and may contribute to the preservation of bone mass observed in hyperinsulinemic states such as obesity.
osteoblast; bone-active hormone; bone anabolic
Address for reprint requests and other correspondence: J. Cornish, Dept. of Medicine, Univ. of Auckland, Private Bag 92019, Auckland, NZ (e-mail: j.cornish{at}auckland.ac.nz )</description><subject>Animals</subject><subject>Bone Development - drug effects</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>Cells, Cultured</subject><subject>Humans</subject><subject>Insulin-Like Growth Factor II - metabolism</subject><subject>Insulin-Like Growth Factor II - pharmacology</subject><subject>Insulin-Secreting Cells - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mitogen-Activated Protein Kinase 1 - metabolism</subject><subject>Mitogen-Activated Protein Kinase 3 - metabolism</subject><subject>Osteoblasts - cytology</subject><subject>Osteoblasts - drug effects</subject><subject>Osteoclasts - metabolism</subject><subject>Osteogenesis - drug effects</subject><subject>Peptide Fragments - metabolism</subject><subject>Peptide Fragments - pharmacology</subject><subject>Peptides - metabolism</subject><subject>Peptides - pharmacology</subject><subject>Pertussis Toxin - pharmacology</subject><subject>Rats</subject><subject>Receptors, Islet Amyloid Polypeptide</subject><subject>Receptors, Peptide - antagonists & inhibitors</subject><subject>Swiss 3T3 Cells</subject><issn>0193-1849</issn><issn>1522-1555</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9PGzEQxa2KqqS0X6CHyidObOrx_vURISiVkNoDPbtee5wYbdaL7QXy7euQIE6IkzWe93t6mkfIN2BLgJr_UHcTjsYvGWsqvuSM1R_IIi94AXVdH5EFA1EW0FXimHyO8Y4x1tYV_0SOoRHAWd0syL8_AafkxjOqRp_WGOi0mw3SKXgz60S9pfmfTmrUAVVymvaYVKFxGM6oi9THhH6FY164kT64FHz2MvvhwX8hH60aIn49vCfk79Xl7cV1cfP756-L85tCV5ylArAy2DOrrIZSoEXWllz1TctVJ8pWmB6M7oFZCx0oJgD7VgNkAntjBZQn5HTvm3PfzxiT3Li4C6lG9HOUTVd2oirZu0IQbce7hmch3wt18DEGtHIKbqPCVgKTuwLkoQD5XIDcFZCh7wf3ud-geUUOF88CsRes3Wr96ALKab2Nzg9-tZVX8zDc4lN6ceaCS5CXAK2cjM1s8Tb7EuaVKf8D8EKpbQ</recordid><startdate>20070101</startdate><enddate>20070101</enddate><creator>Cornish, J</creator><creator>Callon, K. 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R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preptin, another peptide product of the pancreatic beta-cell, is osteogenic in vitro and in vivo</atitle><jtitle>American journal of physiology: endocrinology and metabolism</jtitle><addtitle>Am J Physiol Endocrinol Metab</addtitle><date>2007-01-01</date><risdate>2007</risdate><volume>292</volume><issue>1</issue><spage>E117</spage><epage>E122</epage><pages>E117-E122</pages><issn>0193-1849</issn><eissn>1522-1555</eissn><abstract>1 Department of Medicine and 2 School of Biological Sciences, University of Auckland, Auckland, New Zealand
Submitted 20 December 2005
; accepted in final form 7 August 2006
Several hormones that regulate nutritional status also impact on bone metabolism. Preptin is a recently isolated 34-amino acid peptide hormone that is cosecreted with insulin and amylin from the pancreatic -cells. Preptin corresponds to Asp 69 -Leu 102 of pro-IGF-II. Increased circulating levels of a pro-IGF-II peptide complexed with IGF-binding protein-2 have been implicated in the high bone mass phenotype observed in patients with chronic hepatitis C infection. We have assessed preptin's activities on bone. Preptin dose-dependently stimulated the proliferation (cell number and DNA synthesis) of primary fetal rat osteoblasts and osteoblast-like cell lines at periphysiological concentrations (>10 11 M). In addition, thymidine incorporation was stimulated in murine neonatal calvarial organ culture, likely reflecting the proliferation of cells from the osteoblast lineage. Preptin did not affect bone resorption in this model. Preptin induced phosphorylation of p42/p44 MAP kinases in osteoblastic cells in a dose-dependent manner (10 8 -10 10 M), and its proliferative effects on primary osteoblasts were blocked by MAP kinase kinase inhibitors. Preptin also reduced osteoblast apoptosis induced by serum deprivation, reducing the number of apoptotic cells by >20%. In vivo administration of preptin increased bone area and mineralizing surface in adult mice. These data demonstrate that preptin, which is cosecreted from the pancreatic -cell with amylin and insulin, is anabolic to bone and may contribute to the preservation of bone mass observed in hyperinsulinemic states such as obesity.
osteoblast; bone-active hormone; bone anabolic
Address for reprint requests and other correspondence: J. Cornish, Dept. of Medicine, Univ. of Auckland, Private Bag 92019, Auckland, NZ (e-mail: j.cornish{at}auckland.ac.nz )</abstract><cop>United States</cop><pmid>16912056</pmid><doi>10.1152/ajpendo.00642.2005</doi><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; American Physiological Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Animals Bone Development - drug effects Cell Differentiation - drug effects Cell Proliferation - drug effects Cell Survival - drug effects Cells, Cultured Humans Insulin-Like Growth Factor II - metabolism Insulin-Like Growth Factor II - pharmacology Insulin-Secreting Cells - metabolism Male Mice Mitogen-Activated Protein Kinase 1 - metabolism Mitogen-Activated Protein Kinase 3 - metabolism Osteoblasts - cytology Osteoblasts - drug effects Osteoclasts - metabolism Osteogenesis - drug effects Peptide Fragments - metabolism Peptide Fragments - pharmacology Peptides - metabolism Peptides - pharmacology Pertussis Toxin - pharmacology Rats Receptors, Islet Amyloid Polypeptide Receptors, Peptide - antagonists & inhibitors Swiss 3T3 Cells |
title | Preptin, another peptide product of the pancreatic beta-cell, is osteogenic in vitro and in vivo |
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