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1.
Journal of Southern Medical University ; (12): 317-322, 2014.
Artículo en Chino | WPRIM | ID: wpr-356929

RESUMEN

<p><b>OBJECTIVE</b>To investigate the effect of co-expression of bone morphogenetic protein 2 (BMP2) and Sox9 on chondrogenic differentiation of mesenchymal stem cells (MSCs) in vitro and provide experimental evidence for tissue engineering of cartilage.</p><p><b>METHODS</b>Mouse embryonic bone marrow MSC C3H10T1/2 cells were infected with recombinant adenovirus expressing BMP2, Sox9 and green fluorescent protein (GFP) for 3-14 days, with cells infected with the adenovirus carrying GFP gene as the control. The mRNA expression of the markers of chondrogenic differentiation, including collagen type II (Col2a1), aggrecan (ACAN), and collagen type X (Col10a1), were determined by real-time PCR. Alcian blue staining was used for quantitative analysis of sulfated glycosaminoglycan in the cellular matrix. The expression of Col2a1 protein was assayed by immunohistochemical staining and Western blot analysis.</p><p><b>RESULTS</b>Adenovirus-mediated BMP2 expression induced chondrogenic differentiation of C3H10T1/2 cells. Overexpression of Sox9 effectively enhanced BMP2-induced expression of the chondrogenic markers Col2a1, aggrecan and Col10a1 mRNAs, and promoted the synthesis of sulfated glycosaminoglycan and Col2a1 protein in C3H10T1/2 cells.</p><p><b>CONCLUSION</b>Co-expression of BMP2 and Sox9 can promote chondrogenic differentiation of MSCs in vitro, which provides a new strategy for tissue engineering of cartilage.</p>


Asunto(s)
Animales , Humanos , Ratones , Proteína Morfogenética Ósea 2 , Genética , Metabolismo , Cartílago , Biología Celular , Diferenciación Celular , Células Cultivadas , Condrocitos , Biología Celular , Células Madre Mesenquimatosas , Biología Celular , Metabolismo , Factor de Transcripción SOX9 , Genética , Metabolismo , Ingeniería de Tejidos
2.
Journal of Biomedical Engineering ; (6): 1022-1026, 2013.
Artículo en Chino | WPRIM | ID: wpr-352120

RESUMEN

This paper is aimed to investigate the effect of titanium (Ti) particles and tumor necrosis factor alpha (TNF-alpha) on the expressions of MMP-1, 2, 3 in human synovial cells, so as to explore the possible mechanism of osteolysis post-operation of metal-on-metal total joint arthroplasty in human synovial cells induced by Ti particles. In vitro cell cultures, human synovial cells were treated by Ti particles and/or TNF-alpha. The total RNA was isolated at 2 hours after the treatment. The gene expression of MMP-1, 2, 3 was analyzed by Semi-quantitative Reverse-transcriptional PCR and quantitative real-time PCR. Cell supernatant was collected at 12, 24, 48 hours after the treatment and Gelatin zymography was performed to detect the activity of MMP-2. Compared to those in the control group (untreated), Ti particles and TNF-alpha increased the gene expression of MMP-1, 2, 3 respectively (P < 0.05), and the effect of combination of the two was even more significant (P < 0.01). The trend of activities of MMP-2 is similar with gene expression. Ti particles and TNF-alpha increased MMP-2 activities by 1.3 times and 1.5 times respectively (P < 0.05), and the combination of the two increased by 1.7 times (P < 0.01). Ti particles and TNF-alpha-induced the stimulation of MMP-1, 2, 3 expressions and MMP-2 activities in human knee joint synovial cells may be involved in aseptic loosening after metal-on-metal arthroplasty through increasing the degradation of bone matrix and declining of osseous support structure mechanics.


Asunto(s)
Humanos , Células Cultivadas , Prótesis Articulares , Articulación de la Rodilla , Biología Celular , Metaloproteinasa 1 de la Matriz , Genética , Metabolismo , Metaloproteinasa 2 de la Matriz , Genética , Metabolismo , Metaloproteinasa 3 de la Matriz , Genética , Metabolismo , Metaloproteinasas de la Matriz , Genética , Metabolismo , Tamaño de la Partícula , Falla de Prótesis , ARN , Genética , Metabolismo , Membrana Sinovial , Biología Celular , Titanio , Farmacología , Factor de Necrosis Tumoral alfa , Farmacología
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