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屈肌腱组织工程:生物反应器周期性应变增加构建体强度。

Flexor tendon tissue engineering: bioreactor cyclic strain increases construct strength.

机构信息

Division of Plastic and Reconstructive Surgery, Stanford University Medical Center, Stanford, California, USA.

出版信息

Tissue Eng Part A. 2010 Jun;16(6):2085-90. doi: 10.1089/ten.TEA.2010.0032.

DOI:10.1089/ten.TEA.2010.0032
PMID:20109062
Abstract

Mutilating injuries of the hand and upper extremity result in tendon losses too great to be replaced by autologous grafts. The goal of this study was to use tissue engineering techniques to produce additional tendon material. We used a custom bioreactor to apply cyclic mechanical loading onto tissue-engineered tendon constructs to study ultimate tensile stress (UTS) and elastic modulus (E). Constructs used were acellularized rabbit hindpaw flexor digitorum profundus equivalents reseeded with tenocytes or left unseeded. Tendon constructs were subjected to a stretch force of 1.25 N over a 5-day course. Seeded tendon constructs that were exposed to bioreactor loading had a significantly increased UTS (71.17 +/- 14.15 N) compared to nonloaded controls (35.69 +/- 5.62 N) (p = 0.001). Similarly, seeded constructs exposed to bioreactor loading also had a significantly higher E (1091 +/- 169 MPa) compared to nonloaded controls (632 +/- 86 MPa) (p = 0.001). This study shows that cyclic loading of tendon constructs increases the UTS and elastic modulus of seeded constructs. The use of the bioreactor may therefore accelerate the in vitro production of strong, nonimmunogenic tendon material that can potentially be used clinically to reconstruct significant tendon losses.

摘要

手部和上肢的严重创伤会导致无法用自体移植物替代的肌腱损失。本研究的目的是使用组织工程技术来产生额外的肌腱材料。我们使用定制的生物反应器对组织工程肌腱进行周期性机械加载,以研究极限拉伸应力 (UTS) 和弹性模量 (E)。使用的构建体是去细胞化的兔后足屈趾深肌腱等效物,重新接种肌腱细胞或未接种。肌腱构建体在 5 天的过程中受到 1.25 N 的拉伸力。与未加载的对照组(35.69 +/- 5.62 N)相比,暴露于生物反应器加载的接种肌腱构建体的 UTS(71.17 +/- 14.15 N)显着增加(p = 0.001)。同样,暴露于生物反应器加载的接种构建体的 E(1091 +/- 169 MPa)也明显高于未加载的对照组(632 +/- 86 MPa)(p = 0.001)。这项研究表明,肌腱构建体的周期性加载会增加接种构建体的 UTS 和弹性模量。因此,生物反应器的使用可能会加速强、非免疫原性肌腱材料的体外生产,这些材料有可能在临床上用于重建严重的肌腱损失。

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