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软骨细胞的生理培养。

Physioxic Culture of Chondrogenic Cells.

机构信息

Experimental Trauma Surgery, Department of Trauma Surgery, University Medical Center of Regensburg, Regensburg, Germany.

Department of Orthopaedics & Rehabilitation, Oregon Health & Science University, Portland, OR, USA.

出版信息

Methods Mol Biol. 2023;2598:45-63. doi: 10.1007/978-1-0716-2839-3_5.

Abstract

Cartilage resides under a low oxygen tension within articulating joints. The oxygen tension within cartilage of the knee joint has been measured to be between 2% and 5% oxygen. Although the literature has historically termed this level of oxygen as hypoxia, particularly when doing experiments in vitro in this range, this is actually the physiological oxygen tension experienced in vivo and is more accurately termed physioxia. In general, culture of chondrogenic cells under physioxia has demonstrated a donor-dependent beneficial effect on chondrogenesis, with an upregulation in cartilage genes (SOX9, COL2A1, ACAN) and matrix deposition (sulfated glycosaminoglycans (sGAGs), collagen II). Physioxia also reduces the expression of hypertrophic markers (COL10A1, MMP13). This chapter will outline the methods for the expansion and differentiation of chondrogenic cells under physioxia using oxygen-controlled incubators and glove box environments, with the typical assays used for qualitative and quantitative assessment of chondrogenesis.

摘要

软骨存在于关节活动部位的低氧张力环境下。膝关节软骨内的氧张力被测量为 2%至 5%的氧。尽管文献中传统上将这一氧水平称为缺氧,特别是在该范围内进行体外实验时,但实际上这是体内实际经历的生理氧张力,更准确地称为低氧。一般来说,在低氧条件下培养软骨细胞,在供体依赖性方面对软骨发生有有益的影响,软骨基因(SOX9、COL2A1、ACAN)和基质沉积(硫酸糖胺聚糖(sGAG)、胶原 II)上调。低氧还降低了肥大标志物(COL10A1、MMP13)的表达。本章将概述使用氧控培养箱和手套箱环境在低氧条件下扩增和分化软骨细胞的方法,以及用于定性和定量评估软骨发生的典型检测方法。

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