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Gingival fibroblasts prevent BMP-mediated osteoblastic differentiation.
Ghuman, Mandeep S; Al-Masri, Maher; Xavier, Guilherme; Cobourne, Martyn T; McKay, Ian J; Hughes, Francis J.
Afiliação
  • Ghuman MS; Division of Tissue Engineering and Biophotonics, Dental Institute, King's College London, London, UK.
  • Al-Masri M; BPP Dental Institute, BPP University, Birmingham, UK.
  • Xavier G; Centre for Craniofacial and Regenerative Biology, Dental Institute, King's College London, Guy's Hospital, London, UK.
  • Cobourne MT; Centre for Craniofacial and Regenerative Biology, Dental Institute, King's College London, Guy's Hospital, London, UK.
  • McKay IJ; Department of Adult Oral Health, Institute of Dentistry, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Hughes FJ; Division of Tissue Engineering and Biophotonics, Dental Institute, King's College London, London, UK.
J Periodontal Res ; 54(3): 300-309, 2019 Jun.
Article em En | MEDLINE | ID: mdl-30511378
ABSTRACT

OBJECTIVES:

The inhibitory action of the superficial gingival connective tissues may limit the regenerative potential of alveolar bone in periodontal therapy or dental implant applications. The aims of this study were to investigate the hypothesis that gingival fibroblasts (GF) can inhibit bone morphogenetic protein (BMP)-induced osteoblastic differentiation, to determine their expression of BMP inhibitors, and finally to determine whether reduction of these inhibitors can relieve suppression of osteoblastic differentiation.

METHODS:

Gingival fibroblasts were co-cultured either directly or indirectly with calvarial osteoblasts to assess alkaline phosphatase inhibitory activity, a marker of osteoblastic differentiation. To test total BMP-inhibitory activity of rat GF, conditioned media (GFCM) were collected from cultures. ROS 17/2.8 osteoblastic cells were stimulated with BMP2, together with GFCM. Inhibitor expression was tested using RT-qPCR, Western blotting and in situ hybridization. Removal of inhibitors was carried out using immunoprecipitation beads.

RESULTS:

Co-culture experiments showed GF-secreted factors that inhibit BMP-stimulated ALP activity. 10 ng/ml BMP2 increased alkaline phosphatase expression in ROS cells by 41%. GFCM blocked BMP activity which was equivalent to the activity of 100 ng/ml Noggin, a well-described BMP inhibitor. Cultured gingival fibroblasts constitutively expressed BMP antagonist genes from the same subfamily, Grem1, Grem2 and Nbl1 and the Wnt inhibitor Sfrp1. Gremlin1 (6.7 × reference gene expression) had highest levels of basal expression. ISH analysis showed Gremlin1 expression was restricted to the inner half of the gingival lamina propria and the PDL. Removal of Gremlin1 protein from GFCM eliminated the inhibitory effect of GFCM on ALP activity in ROS cells. Subsequent addition of recombinant Gremlin1 restored the inhibitory activity.

CONCLUSIONS:

Factors secreted by gingival fibroblasts inhibit BMP-induced bone formation and a range of BMP inhibitors are constitutively expressed in gingival connective tissues. These inhibitors, particularly Gremlin1, may limit coronal alveolar bone regenerative potential during oral and periodontal surgery.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoblastos / Osteogênese / Diferenciação Celular / Proteína Morfogenética Óssea 2 / Fibroblastos / Gengiva Limite: Animals Idioma: En Revista: J Periodontal Res Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteoblastos / Osteogênese / Diferenciação Celular / Proteína Morfogenética Óssea 2 / Fibroblastos / Gengiva Limite: Animals Idioma: En Revista: J Periodontal Res Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Reino Unido