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Behaviour of rat‐cultured dental pulp cells in three‐dimensional collagen type‐1 gel in vitro and in vivo
Author(s) -
Khan Sultan Zeb,
Kokubu Eitoyo,
Matsuzaka Kenichi,
Inoue Takashi
Publication year - 2013
Publication title -
australian endodontic journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.703
H-Index - 34
eISSN - 1747-4477
pISSN - 1329-1947
DOI - 10.1111/j.1747-4477.2012.00351.x
Subject(s) - bone sialoprotein , osteopontin , in vivo , alkaline phosphatase , type i collagen , in vitro , chemistry , osteocalcin , immunohistochemistry , dentin , pulp (tooth) , microbiology and biotechnology , pathology , immunology , biochemistry , biology , medicine , enzyme
The purpose of this study was to investigate the growth and differentiation potential of dental pulp cells (DPCs) in three‐dimensional (3‐D) collagen type‐1 scaffold in vitro and in vivo . Third passage DPCs were cultured in a 3‐D collagen and expression of both bone‐ or dentin‐related mRNA (alkaline phosphatase (ALP), bone sialoprotein (BSP) and osteopontin (OPN)) and morphological changes evaluated in vitro . In the in vivo study, two types of grafts were transplanted into the rectus abdominus muscles of rats and harvested after 7 days: DPCs in α‐minimal essential medium and DPCs mixed with a collagen gel. ALP, BSP and OPN were used as primary antibodies for immunohistochemical study. Histological and immunohistochemical results showed that DPCs in collagen gel were spindle shaped and showed significantly greater expression of ALP, BSP and OPN in vitro than the controls. Transplanted DPCs in collagen type‐1 gel showed greater positive immunoreactivity for ALP, BSP and OPN than the controls. It was concluded that the collagen gel scaffold encouraged the differentiation of DPCs into osteoblastic cells.