Literature DB >> 7999633

Expression and localization of sulphated glycoprotein-2 mRNA in the rat incisor tooth ameloblasts: relationships with apoptosis.

B K Joseph1, G C Gobé, N W Savage, W G Young.   

Abstract

The expression of sulphated glycoprotein-2 (SGP-2) is associated with the onset of cellular atrophy and death in many rodent tissues. This gene has a multifunctional involvement that includes apoptosis, spermatogenesis, promotion of cell-cell interactions, modulation of complement systems and tissue regeneration and remodelling. Using decalcified mandibles, mRNA for SGP-2 in rat incisor tooth ameloblasts was examined by in situ hybridization using 35S riboprobes. The rat incisor is unique in that, at one time, all stages of the complex life cycle of the ameloblasts are represented along the length of the enamel forming aspect of the tooth. The pre-ameloblasts only secrete enamel matrix after mitosis. When the full thickness of the enamel has been formed, a remarkable transition in phenotype takes place in the ameloblast. This transition is accompanied by apoptosis or programmed cell death of approximately 25% of ameloblasts. An additional 25% of ameloblasts undergo apoptosis when maturation of enamel matrix takes place with removal of water and protein from the increasingly mineralized matrix. In the present study, expression of SGP-2 was localized most often in the post-secretory transition and maturation ameloblasts. In contrast, the presecretory and secretory ameloblasts did not demonstrate specific hybridization signals. Consistently, neither the odontoblasts nor the pulp demonstrated hybridization signals. Hence our results support other published results which show that increased expression of SGP-2 is associated with apoptosis. The exact function of the SGP-2 gene and its products is not fully defined.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1994        PMID: 7999633      PMCID: PMC2001862     

Source DB:  PubMed          Journal:  Int J Exp Pathol        ISSN: 0959-9673            Impact factor:   1.925


  33 in total

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Journal:  J Pathol       Date:  1984-01       Impact factor: 7.996

7.  Inhibition of programmed cell death in mouse embryonic palate in vitro by cortisol and phenytoin: receptor involvement and requirement of protein synthesis.

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Journal:  Prostate       Date:  1986       Impact factor: 4.104

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Authors:  B K Joseph; N W Savage; W G Young; G S Gupta; B H Breier; M J Waters
Journal:  Growth Factors       Date:  1993       Impact factor: 2.511

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Journal:  Lab Invest       Date:  1987-03       Impact factor: 5.662

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  2 in total

1.  DNA localization in nuclear fragments of apoptotic ameloblasts using anti-DNA immunoelectron microscopy: programmed cell death of ameloblasts.

Authors:  S Nishikawa; F Sasaki
Journal:  Histochem Cell Biol       Date:  1995-08       Impact factor: 4.304

2.  Loss of BMP2 and BMP4 Signaling in the Dental Epithelium Causes Defective Enamel Maturation and Aberrant Development of Ameloblasts.

Authors:  Claes-Göran Reibring; Maha El Shahawy; Kristina Hallberg; Brian D Harfe; Anders Linde; Amel Gritli-Linde
Journal:  Int J Mol Sci       Date:  2022-05-29       Impact factor: 6.208

  2 in total

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