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机械刺激联合诱导因子对组织工程软骨的影响

[Effect of mechanical stimulation combined with inductive factors on tissue engineered cartilage].

作者信息

Wang Hui, Cui Yimin, Zhu Junfeng, Zhou Xiande, Zhu Chuanmin, Chen Xiaodong

机构信息

Department of Orthopaedics, Affiliated Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200092, PR China.

出版信息

Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2011 Nov;25(11):1377-82.

Abstract

OBJECTIVE

Mechanical stimulation and inductive factors are both crucial aspects in tissue engineered cartilage. To evaluate the effects of mechanical stimulation combined with inductive factors on the differentiation of tissue engineered cartilage.

METHODS

Bone marrow mesenchymal stem cells (BMSCs) were isolated from newborn porcine (aged 7 days and weighing 3-6 kg) and expanded in vitro. The BMSCs at passage 2 were seeded onto a scaffold of poly (lactic-co-glycolic acid) (PLGA) in the concentration of 5 x 10(7)/mL to prepare cell-scaffold composite. Cell-scaffold composites were cultivated in a medium with chondrocyte-inducted factors (group A), in a vessel with mechanic stimulating only (group B), or mechanic stimulating combined with chondrocyte-inducted factors (group C) (parameters of mechanics: 1 Hz, 0.5 MPa, and 4 hours/day). Cell-scaffold composite and auto-cartilage served as positive control (group D) and negative control (group E), respectively. After 4 weeks of cultivation, the thickness, elastic modulus, and glycosaminoglycan (GAG) content of composites were measured. Additionally, BMSCs chondrogenic differentiation was assessed via real-time fluorescent quantitative PCR, immunohistochemistry, and histological staining.

RESULTS

The thickness, elastic modulus, and maximum load in group C were significantly higher than those in groups A and B (P < 0.05). In groups A, B, and C, cartilage lacuna formation, GAG expression, and positive results for collagen type II were observed through HE staining, Safranin-O staining, and immunohistochemistry staining. The dyeing depth was deeper in group A than in group B, and in group C than in groups A and B; group C was close to group E. The GAG content in group C was significantly higher than that in groups A and B (P < 0.05). Real-time fluorescent quantitative PCR revealed that mRNA expressions of collagen type I, collagen type II, and GAG in group C were significantly higher than those in groups A and B (P < 0.05), and in group A than in group B (P < 0.05).

CONCLUSION

Mechanical stimulation combined with chondrocyte inductive factors can enhance the mechanical properties of the composite and induce higher expression of collagen and GAG of BMSCs.

摘要

目的

机械刺激和诱导因子都是组织工程软骨的关键方面。旨在评估机械刺激联合诱导因子对组织工程软骨分化的影响。

方法

从新生猪(7日龄,体重3 - 6千克)分离骨髓间充质干细胞(BMSCs)并在体外扩增。将第2代BMSCs以5×10(7)/mL的浓度接种到聚乳酸-乙醇酸共聚物(PLGA)支架上制备细胞-支架复合物。细胞-支架复合物在含有软骨细胞诱导因子的培养基中培养(A组),在仅进行机械刺激的容器中培养(B组),或在机械刺激联合软骨细胞诱导因子的条件下培养(C组)(力学参数:1Hz,0.5MPa,每天4小时)。细胞-支架复合物和自体软骨分别作为阳性对照(D组)和阴性对照(E组)。培养4周后,测量复合物的厚度、弹性模量和糖胺聚糖(GAG)含量。此外,通过实时荧光定量PCR、免疫组织化学和组织学染色评估BMSCs的软骨分化情况。

结果

C组的厚度、弹性模量和最大负荷显著高于A组和B组(P < 0.05)。通过HE染色、番红O染色和免疫组织化学染色,在A、B、C组中均观察到软骨陷窝形成、GAG表达及Ⅱ型胶原阳性结果。A组的染色深度比B组深,C组比A组和B组深;C组接近E组。C组的GAG含量显著高于A组和B组(P < 0.05)。实时荧光定量PCR显示,C组中Ⅰ型胶原、Ⅱ型胶原和GAG的mRNA表达显著高于A组和B组(P < 0.05),且A组高于B组(P < 0.05)。

结论

机械刺激联合软骨细胞诱导因子可增强复合物的力学性能,并诱导BMSCs中胶原和GAG的高表达。

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