首页> 外文期刊>Journal of orthopaedic research >Additive effects of hyperbaric oxygen and platelet-derived growth factor-BB in chondrocyte transplantation via up-regulation expression of platelet-derived growth factor-beta receptor.
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Additive effects of hyperbaric oxygen and platelet-derived growth factor-BB in chondrocyte transplantation via up-regulation expression of platelet-derived growth factor-beta receptor.

机译:高压氧和血小板衍生的生长因子-BB通过上调血小板衍生的生长因子-β受体的表达在软骨细胞移植中的累加作用。

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摘要

The present study investigated the effects of hyperbaric oxygen (HBO) and platelet-derived growth factor-BB (PDGF-BB) in chondrocyte transplantation. In vitro, chondrocytes were treated with HBO, PDGF-BB, and HBO combined with PDGF-BB (H+P). Cell growth was analyzed using cell counting, MTT assay, and FACS analysis. mRNA expression of the PDGF-alpha receptor (PDGFR-alpha) and beta receptor (PDGFR-beta) was detected by RT-PCR. Protein expression of PDGFR-beta was detected by Western blotting. In vivo, chondrocytes and PDGF-BB were suspended in alginate as a transplantation system. Cartilage defects were grafted with this system and with or without HBO treatment. Released PDGF-BB concentration was quantified by ELISA. After 8 weeks, animals were sacrificed and the repaired tissues were examined. In vitro data suggested that each treatment increased cell growth via the up-regulated mRNA expression of PDGFR-alpha and increased cell accumulation in the S-phase. The H+P treatment was more additive in cell growth and in mRNA and protein expression of PDGFR-beta than HBO or PDGF-BB. In vivo results suggested that PDGF-BB delivery lasted for more than 5 weeks. Scoring results showed that each treatment significantly increased the cartilage repair. Safranin-O and type II collagen staining confirmed the hyaline-like cartilage regeneration in the repaired tissues. In situ up-regulation of PDGFR-beta expression partially explains the additive effect of H+P treatment in cartilage repair. Accordingly, H+P offers a potential treatment method for cartilage repair.
机译:本研究调查了高压氧(HBO)和血小板源性生长因子-BB(PDGF-BB)在软骨细胞移植中的作用。在体外,用HBO,PDGF-BB和HBO结合PDGF-BB(H + P)处理软骨细胞。使用细胞计数,MTT测定和FACS分析来分析细胞生长。通过RT-PCR检测PDGF-α受体(PDGFR-α)和β受体(PDGFR-β)的mRNA表达。通过蛋白质印迹检测PDGFR-β的蛋白质表达。在体内,将软骨细胞和PDGF-BB悬浮在藻酸盐中作为移植系统。使用该系统以及是否进行HBO治疗都可以移植软骨缺损。通过ELISA定量释放的PDGF-BB浓度。 8周后,处死动物并检查修复的组织。体外数据表明,每种治疗均通过上调PDGFR-α的mRNA表达来增加细胞生长,并增加S期的细胞蓄积。与HBO或PDGF-BB相比,H + P处理在细胞生长以及PDGFR-beta的mRNA和蛋白质表达上具有更多的加性。体内结果提示PDGF-BB的递送持续超过5周。计分结果表明,每种治疗均显着增加了软骨修复。番红O和II型胶原染色证实了修复组织中的透明样软骨再生。 PDGFR-β表达的原位上调部分解释了H + P治疗在软骨修复中的累加作用。因此,H + P为软骨修复提供了一种潜在的治疗方法。

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