Literature DB >> 2827713

The effects of inhibitors of cysteine-proteinases and collagenase on the resorptive activity of isolated osteoclasts.

J M Delaisse1, A Boyde, E Maconnachie, N N Ali, C H Sear, Y Eeckhout, G Vaes, S J Jones.   

Abstract

The effects of specific inhibitors of cysteine-proteinases ((Z-Phe-Ala-CHN2: benzyloxycarbonyl-phenyl-alanyl alanyl diazomethane and E-64: trans-epoxy-succinyl-L-leucylamido(4-guanidino)-butane) and collagenase and collagenase ((Cl-1: N-(3-N-benzyloxycarbonyl amino-1-R-carboxypropyl)-L-leucyl-O-methyl-L-tyrosine N-methylamide) have been tested on the osteoclastic resorption of dentine. Chick osteoclasts were cultured in the presence or absence of 12.5 microM Z-Phe-Ala-CHN2, 40 or 60 microM E-64, or 40 or 100 microM Cl-1 for 1 or 2 days. In addition, osteoclasts were cultured on oyster shell calcitostracum with or without 12.5 microM Z-Phe-Ala-CHN2. Specimens were studied by light microscopy to count cells and resorption features and by scanning electron microscopy (SEM) stereophotogrammetry for the measurement of the depths, plan-areas and volumes of resorption pits. The numbers, depths and volumes (but not the plan-areas) of the resorption pits in dentine were significantly reduced by Z-Phe-Ala-CHN2 and E-64. Thus, for a given plan-area, the volumes and the depths of resorption pits were smaller in these experimental groups compared with control dentine specimens. The overall inhibition of resorption was at least 75%. Cl-1 did not have this inhibitory effect on the numbers or sizes of resorption pits in dentine. When the oyster calcitostracum was used as a substrate for the osteoclasts, Z-Phe-Ala-CHN2 did not reduce the numbers or volumes of pits, but increased the plan-areas and prevented the formation of deeper pits.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1987        PMID: 2827713     DOI: 10.1016/8756-3282(87)90007-x

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  20 in total

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Authors:  K Piper; A Boyde; S J Jones
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2.  Pitfalls in pit measurement.

Authors:  A Boyde; S J Jones
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3.  An ultrastructural evaluation of the effects of cysteine-proteinase inhibitors on osteoclastic resorptive functions.

Authors:  K Debari; T Sasaki; N Udagawa; B R Rifkin
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4.  Voltage-activated K+ conductances in freshly isolated embryonic chicken osteoclasts.

Authors:  J H Ravesloot; D L Ypey; T Vrijheid-Lammers; P J Nijweide
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5.  Cysteine-proteinase localization in osteoclasts: an immunocytochemical study.

Authors:  T Sasaki; E Ueno-Matsuda
Journal:  Cell Tissue Res       Date:  1993-01       Impact factor: 5.249

6.  Immunohistochemical localization of cathepsins B, D and L in the rat osteoclast.

Authors:  T Goto; T Tsukuba; T Kiyoshima; Y Nishimura; K Kato; K Yamamoto; T Tanaka
Journal:  Histochemistry       Date:  1993-05

7.  Inhibition of bone resorption in vitro by selective inhibitors of gelatinase and collagenase.

Authors:  P A Hill; A J Docherty; K M Bottomley; J P O'Connell; J R Morphy; J J Reynolds; M C Meikle
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8.  Alterations in osteoclast function and phenotype induced by different inhibitors of bone resorption--implications for osteoclast quality.

Authors:  Anita V Neutzsky-Wulff; Mette G Sørensen; Dino Kocijancic; Diana J Leeming; Morten H Dziegiel; Morten A Karsdal; Kim Henriksen
Journal:  BMC Musculoskelet Disord       Date:  2010-06-01       Impact factor: 2.362

9.  Collagenolytic cysteine proteinases of bone tissue. Cathepsin B, (pro)cathepsin L and a cathepsin L-like 70 kDa proteinase.

Authors:  J M Delaissé; P Ledent; G Vaes
Journal:  Biochem J       Date:  1991-10-01       Impact factor: 3.857

Review 10.  Cathepsin K inhibitors for osteoporosis and potential off-target effects.

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Journal:  Expert Opin Investig Drugs       Date:  2009-05       Impact factor: 6.206

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