Literature DB >> 8882154

Parathyroid hormone-related protein (PTHrP) action in rat articular chondrocytes: comparison of PTH(1-34), PTHrP(1-34), PTHrP(1-141), PTHrP(100-114) and antisense oligonucleotides against PTHrP.

T Tsukazaki1, A Ohtsuru, H Namba, J Oda, K Motomura, M Osaki, T Kiriyama, K Iwasaki, S Yamashita.   

Abstract

Parathyroid hormone-related protein (PTHrP) is thought to be an important autocrine/paracrine factor for chondrocyte metabolism since mice lacking the PTHrP gene exhibit abnormal cartilage development. To determine the biological role of PTHrP in chondrocytes, we first compared the agonist potency of human (h) PTHrP(1-34) with hPTH(1-34) in cultured rat articular chondrocytes. Neither hPTHrP(1-34) nor hPTH(1-34) altered basal DNA synthesis, but attenuated the stimulatory effect of transforming growth factor beta (TGF-beta). Both agents suppressed the expression of alpha(1) type II collagen mRNA in a dose-response fashion with the same potency. In addition, the action of exogenously added hPTHrP(1-34) and hPTH(1-34) on intracellular cAMP and [Ca2+]i levels was similar. We next compared the effect of PTHrP within its entire amino acid sequence (1-141). With regard to thymidine incorporation, alpha(1) type II collagen gene expression and accumulation of cAMP and [Ca2+]i level, there was no significant difference between hPTHrP(1-34) and hPTHrP(1-141). PTHrP C-terminal (100-114) did not show any function. To further investigate PTHrP function, intracellular PTHrP translation was inhibited by a transgene of antisense oligonucleotides against PTHrP. Antisense oligonucleotides decreased PTHrP mRNA translation, specifically inhibited DNA synthesis in control as well as TGF-beta-treated chondrocytes and enhanced alpha(1) type II collagen mRNA expression in TGF-beta-treated chondrocytes. These results suggest that there is no significant difference between exogenously added hPTH(1-34), hPTHrP(1-34) and PTHrP(1-141) with regard to the biological action of these agents, including cell growth, differentiation and second messenger pathway. However, the result of DNA synthesis in the antisense PTHrP-inhibition study suggests that intracellular PTHrP may have an as yet unknown biological role, in addition to a classical PTH/PTHrP receptor-mediated function in the rat articular chondrocyte.

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Year:  1996        PMID: 8882154     DOI: 10.1677/joe.0.1500359

Source DB:  PubMed          Journal:  J Endocrinol        ISSN: 0022-0795            Impact factor:   4.286


  7 in total

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Authors:  E Nasatzky; E Azran; D D Dean; B D Boyan; Z Schwartz
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Authors:  Tri Dung Tiet; Sevan Hopyan; Puviindran Nadesan; Nalan Gokgoz; Raymond Poon; Alvin C Lin; Taiqiang Yan; Irene L Andrulis; Benjamin A Alman; Jay S Wunder
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3.  The chondrogenic transcription factor Sox9 is a target of signaling by the parathyroid hormone-related peptide in the growth plate of endochondral bones.

Authors:  W Huang; U I Chung; H M Kronenberg; B de Crombrugghe
Journal:  Proc Natl Acad Sci U S A       Date:  2001-01-02       Impact factor: 11.205

Review 4.  Fracture healing physiology and the quest for therapies for delayed healing and nonunion.

Authors:  Paul Kostenuik; Faisal M Mirza
Journal:  J Orthop Res       Date:  2016-12-19       Impact factor: 3.494

5.  PTH decreases in vitro human cartilage regeneration without affecting hypertrophic differentiation.

Authors:  Marijn Rutgers; Frances Bach; Luciënne Vonk; Mattie van Rijen; Vanessa Akrum; Antonette van Boxtel; Wouter Dhert; Laura Creemers
Journal:  PLoS One       Date:  2019-04-04       Impact factor: 3.240

6.  Deletion of the nuclear localization sequence and C-terminus of parathyroid hormone-related protein decreases osteogenesis and chondrogenesis but increases adipogenesis and myogenesis in murine bone marrow stromal cells.

Authors:  Blake E Hildreth; Krista M Hernon; Wessel P Dirksen; John Leong; Wachiraphan Supsavhad; Prosper N Boyaka; Thomas J Rosol; Ramiro E Toribio
Journal:  J Tissue Eng       Date:  2015-10-12       Impact factor: 7.813

7.  Altered expression of inflammatory cytokines in primary osteoarthritis by human T lymphotropic virus type I retrovirus infection: a cross-sectional study.

Authors:  Yoshiki Yoshihara; Tomoo Tsukazaki; Makoto Osaki; Masahiro Nakashima; Kazuhisa Hasui; Hiroyuki Shindo
Journal:  Arthritis Res Ther       Date:  2004-06-07       Impact factor: 5.156

  7 in total

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