作者: Emmanuel Soffer , Jean-Pierre Ouhayoun , Christine Dosquet , Alain Meunier , Fani Anagnostou
DOI: 10.1111/J.1600-0501.2004.01063.X
关键词: Alkaline phosphatase 、 Immunology 、 Platelet 、 Molecular biology 、 Bone cell 、 Collagenase 、 Platelet lysate 、 Calvaria 、 Cell migration 、 Biology 、 Bone healing
摘要: Although platelet-rich plasma and platelet concentrates have been used to promote bone healing in orthopaedic maxillofacial surgery, the underlying cellular-level mechanisms remain poorly understood. The present vitro study investigated effects of human lysate (PL) on selected functions cultured cells. Cells from 18-day-old fetal rat calvaria were isolated by a collagenase digestion procedure. PL was added at different concentrations pre- or post-confluent cell stage. After 1 day, proliferation maximal half-maximal presence 3 x 10(8) 0.5 platelets/ml, respectively. During 17 h, number cells traversing scrape border wound model increased 16-fold platelets/ml. platelets/ml pre-confluent cultures for 48 h resulted threefold decrease alkaline phosphatase (ALP) specific activity. In case confluent cells, (from 10(6) platelets/ml) 11 days, ALP activity total calcium content decreased dose-dependent manner reached minimum summary, short-term exposure (up 24 h) promotes proliferative chemotactic while long-term results both mineral formation. These data show that soluble components contained may affect process modulating differently functions.