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J Biomech Eng. 2009 Oct;131(10):101002. doi: 10.1115/1.3192139.
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Shape, loading, and motion in the bioengineering design, fabrication, and testing of personalized synovial joints.在个性化滑膜关节的生物工程设计、制造和测试中,形状、载荷和运动。
J Biomech. 2010 Jan 5;43(1):156-65. doi: 10.1016/j.jbiomech.2009.09.021. Epub 2009 Oct 7.
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Non-surgical correction of congenital deformities of the auricle: a systematic review of the literature.先天性耳廓畸形的非手术矫正:文献系统综述
J Plast Reconstr Aesthet Surg. 2009 Jun;62(6):727-36. doi: 10.1016/j.bjps.2009.01.020. Epub 2009 Mar 27.
4
Asymmetrical strain distributions and neutral axis location of cartilage in flexure.软骨在弯曲时的不对称应变分布和中性轴位置。
J Biomech. 2009 Feb 9;42(3):325-30. doi: 10.1016/j.jbiomech.2008.11.009. Epub 2008 Dec 30.
5
Articular cartilage tensile integrity: modulation by matrix depletion is maturation-dependent.关节软骨拉伸完整性:基质损耗的调节取决于成熟度。
Arch Biochem Biophys. 2008 Jun 1;474(1):175-82. doi: 10.1016/j.abb.2008.03.012. Epub 2008 Mar 21.
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Guided cartilage regeneration using resorbable template.使用可吸收模板引导软骨再生。
Eplasty. 2007 Jan 3;8:e5.
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Regulation of immature cartilage growth by IGF-I, TGF-beta1, BMP-7, and PDGF-AB: role of metabolic balance between fixed charge and collagen network.胰岛素样生长因子-I(IGF-I)、转化生长因子-β1(TGF-β1)、骨形态发生蛋白-7(BMP-7)和血小板衍生生长因子-AB(PDGF-AB)对未成熟软骨生长的调节:固定电荷与胶原网络之间代谢平衡的作用
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8
Cartilage reshaping via in vitro mechanical loading.通过体外机械加载进行软骨重塑。
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9
Cartilage growth and remodeling: modulation of balance between proteoglycan and collagen network in vitro with beta-aminopropionitrile.软骨生长与重塑:β-氨基丙腈对体外蛋白聚糖与胶原网络平衡的调节作用
Osteoarthritis Cartilage. 2008 Jan;16(1):1-11. doi: 10.1016/j.joca.2007.05.019. Epub 2007 Jul 16.
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通过基质重塑的生化调节体外调节软骨形状可塑性。

In vitro modulation of cartilage shape plasticity by biochemical regulation of matrix remodeling.

机构信息

Department of Bioengineering, University of California, San Diego, La Jolla, California 92093, USA.

出版信息

Tissue Eng Part A. 2011 Jan;17(1-2):17-23. doi: 10.1089/ten.TEA.2010.0177. Epub 2010 Oct 8.

DOI:10.1089/ten.TEA.2010.0177
PMID:20649477
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3011909/
Abstract

With consideration of the need for cartilage grafts of specific sizes and shapes in orthopedics and other fields, immature cartilage explants and grafts have recently been molded in vitro and in vivo. Nonsurgical correction of cartilage deformities and malformations often uses mechanical stimuli and further demonstrates the plasticity of cartilage shape. Cartilage shape plasticity appears to diminish with maturation, coincident with changes in matrix composition. This study's objectives were to characterize shape plasticity of articular cartilage from immature and mature bovines and test whether altering proteoglycan and collagen (COL) remodeling modulates shape plasticity in vitro. Cartilage explants were analyzed fresh on day 0 or after 14 days of culture in the presence of β-D-xyloside to suppress glycosaminoglycan accumulation or β-aminopropionitrile (BAPN) to inhibit lysyl oxidase-mediated COL crosslinking. Culture with β-d-xyloside and BAPN differentially regulated cartilage size, composition, and shape plasticity, with an inverse association between shape plasticity and the ratio of tissue COL to glycosaminoglycan. Retention of a mechanically imposed contour was increased by culture with BAPN compared to day 0 calf cartilage (90% vs. 69%), and BAPN-treated samples had higher shape retention than β-D-xyloside-treated samples for both calf (90% vs. 74%) and adult cartilage (54% vs. 31%). The findings provide quantitative measures of cartilage shape plasticity at immature and mature stages and are consistent with the concept of diminishing shape plasticity with maturation. The ability to modulate cartilage shape plasticity by varying in vitro biochemical conditions may be a useful tool for the formation of contoured chondral grafts.

摘要

考虑到矫形科和其他领域对特定大小和形状的软骨移植物的需求,最近已经在体外和体内对未成熟的软骨外植体和移植物进行了成型。非手术矫正软骨畸形和畸形通常使用机械刺激,并进一步证明了软骨形状的可塑性。软骨形状的可塑性似乎随着成熟而减少,与基质成分的变化一致。本研究的目的是描述来自未成熟和成熟牛的关节软骨的形状可塑性,并测试改变蛋白聚糖和胶原蛋白(COL)重塑是否能调节体外的形状可塑性。软骨外植体在第 0 天或在存在β-D-木糖的情况下培养 14 天后进行新鲜分析,以抑制糖胺聚糖的积累,或用β-氨基丙腈(BAPN)抑制赖氨酰氧化酶介导的 COL 交联。β-D-木糖和 BAPN 的培养差异调节软骨的大小、组成和形状可塑性,形状可塑性与组织 COL 与糖胺聚糖的比例呈反比。与第 0 天小牛软骨(90%比 69%)相比,BAPN 培养增加了机械施加轮廓的保留率,并且 BAPN 处理的样本比β-D-木糖处理的样本具有更高的形状保留率,无论是小牛(90%比 74%)还是成人软骨(54%比 31%)。这些发现提供了未成熟和成熟阶段软骨形状可塑性的定量测量值,与成熟时形状可塑性降低的概念一致。通过改变体外生化条件来调节软骨形状可塑性的能力可能是形成轮廓软骨移植物的有用工具。