



@article {2577,
	title = {In vitro osteoblastic differentiation of human bone marrow cells in the presence of metal ions},
	journal = {Journal of Biomedical Materials ResearchJ. Biomed. Mater. Res.},
	volume = {44},
	year = {1999},
	note = {Cited By (since 1996): 35Export Date: 21 November 2012Source: ScopusCODEN: JBMRBdoi: 10.1002/(SICI)1097-4636(199902)44:2<176::AID-JBM8>3.0.CO;2-6PubMed ID: 10397919Language of Original Document: EnglishCorrespondence Address: Fernandes, M.H.; Faculdade de Medicina Dentaria, Universidade do Porto, Rua Dr Manuel Pereira da Silva, 4200 Porto, PortugalChemicals/CAS: Alkaline Phosphatase, EC 3.1.3.1; Alloys; Biocompatible Materials; Calcium, 7440-70-2; Chromium, 7440-47-3; Iron, 7439-89-6; Metals; Nickel, 7440-02-0; Phosphorus, 7723-14-0; Proteins; Stainless Steel, 12597-68-1; Tetrazolium Salts; Thiazoles; thiazolyl blue, 298-93-1References: Williams, D., Cahn, R.W., Bever, M.B., (1990) Concise Encyclopedia of Medical \& Dental Materials, pp. 4-70. , Oxford, New York, Beijing, Frankfurt, S{\~a}o Paulo, Sydney, Tokyo, Toronto: Permagon Press;Linden, J.V., Hopler, S.M., Gossling, H.R., Sunderman Jr., F.W., Blood nickel concentrations in patients with stainless-steel hip protheses (1985) Ann Clin Lab Sci, 15, pp. 459-464. , 1985; 
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},
	month = {1999///},
	pages = {176 - 190},
	publisher = {John Wiley \& Sons Inc},
	abstract = {For periods up to 21 days human bone marrow was cultured in control conditions that favor the proliferation and differentiation of osteoblastic cells. The effect of AISI 316L corrosion products and the corresponding major separate metal ions (Fe, Cr, and Ni) were studied in three different phases of the culture period in order to investigate the effects of metal ions in cell populations representative of osteoblastic cells in different stages of differentiation. Toxicity consequences of the presence of metal ions in bone marrow cultures were evaluated by biochemical parameters (enzymatic reduction of MTT, alkaline phosphatase activity, and total protein content), histochemical assays (identification of ALP-positive cells and Ca and phosphates deposits), and observation of the cultures by light and scanning electron microscopy. Culture media were analyzed for total and ionized Ca and P and also for metal ions (Fe, Cr, and Ni). The presence of AISI 316L corrosion products and Ni salt in bone marrow cultures during the first and second weeks of culture significantly disturbs the normal behavior of these cultures, interfering in the lag phase and exponential phase of cell growth and ALP expression. However, the presence of these species during the third week of culture, when expression of osteoblastic functions occurs (mineralization process), did not result in any detectable effect. Fe salt also disturbs the behavior of bone marrow cell cultures when present during the lag phase and proliferation phase, and a somewhat compromised response between the normal pattern (control cultures) and intense inhibition (AISI 316L corrosion products and Ni salt-added cultures) was observed. Fe did not affect the progression of the mineralization phase. Osteogenic cultures exposed to Cr salt (Cr                        3+) presented a pattern similar to the controls, indicating that this element does not interfere, in the concentration studied, in the osteoblastic differentiation of bone marrow cells. Quantification of metal ions in the culture media showed that Cr (originated from AISI 316L corrosion products but from not Cr
                        3+ salt) and Ni (originated from AISI 316L corrosion products and Ni salt) appear to be retained by the bone marrow cultures.
For periods up to 21 days human bone marrow was cultured in control conditions that favor the proliferation and differentiation of osteoblastic cells. The effect of AISI 316L corrosion products and the corresponding major separate metal ions (Fe, Cr, and Ni) were studied in three different phases of the culture period in order to investigate the effects of metal ions in cell populations representative of osteoblastic cells in different stages of differentiation. Toxicity consequences of the presence of metal ions in bone marrow cultures were evaluated by biochemical parameters (enzymatic reduction of MTT, alkaline phosphatase activity, and total protein content), histochemical assays (identification of ALP-positive cells and Ca and phosphates deposits), and observation of the cultures by light and scanning electron microscopy. Culture media were analyzed for total and ionized Ca and P and also for metal ions (Fe, Cr, and Ni). The presence of AISI 316L corrosion products and Ni salt in bone marrow cultures during the first and second weeks of culture significantly disturbs the normal behavior of these cultures, interfering in the lag phase and exponential phase of cell growth and ALP expression. However, the presence of these species during the third week of culture, when expression of osteoblastic functions occurs (mineralization process), did not result in any detectable effect. Fe salt also disturbs the behavior of bone marrow cell cultures when present during the lag phase and proliferation phase, and a somewhat compromised response between the normal pattern (control cultures) and intense inhibition (AISI 316L corrosion products and Ni salt-added cultures) was observed. Fe did not affect the progression of the mineralization phase. Osteogenic cultures exposed to Cr salt (Cr
                        3+) presented a pattern similar to the controls, indicating that this element does not interfere, in the concentration studied, in the osteoblastic differentiation of bone marrow cells. Quantification of metal ions in the culture media showed that Cr (originated from AISI 316L corrosion products but from not Cr
                        3+ salt) and Ni (originated from AISI 316L corrosion products and Ni salt) appear to be retained by the bone marrow cultures.
},
	keywords = {alkaline phosphatase, Alloys, article, Batch cell culture, Biocompatible Materials, biotechnology, Bone, Bone cells, bone marrow cell, Bone Marrow Cells, bone mineralization, bone prosthesis, Calcium, Cell culture, cell differentiation, Cell Division, cell population, Cells, Cultured, Chromium, controlled study, Corrosion, Corrosion products, Cytotoxicity, Differentiation, human, human cell, Human osteoblast-like cells, Humans, Implants (surgical), Ions, Iron, joint prosthesis, materials testing, metal ion, Metal ions, Metals, Nickel, osteoblast, Osteoblasts, phosphorus, Prostheses and Implants, Proteins, Stainless steel, Steel corrosion, Tetrazolium Salts, Thiazoles},
	isbn = {00219304 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-0033080559\&partnerID=40\&md5=721fda55da342bbc327b233d73789014},
	author = {Morais, S. and Dias, N. and Sousa, J.P. and Fernandes, M.H. and Carvalho, G.S.}
}
