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用于治疗椎间盘退变的聚合物水凝胶干细胞递送:从三维培养到微创治疗递送装置的设计

Stem Cell Delivery With Polymer Hydrogel for Treatment of Intervertebral Disc Degeneration: From 3D Culture to Design of the Delivery Device for Minimally Invasive Therapy.

作者信息

Kumar Deepak, Lyness Alex, Gerges Irini, Lenardi Christina, Forsyth Nicholas R, Liu Yang

出版信息

Cell Transplant. 2016 Dec 13;25(12):2213-2220. doi: 10.3727/096368916X692618. Epub 2016 Jul 22.

DOI:10.3727/096368916X692618
PMID:27452665
Abstract

Nucleus pulposus (NP) tissue damage can induce detrimental mechanical strain on the biomechanical performance of intervertebral discs (IVDs), causing subsequent disc degeneration. A novel, photocurable, injectable, synthetic polymer hydrogel (pHEMA-co-APMA grafted with PAA) has already demonstrated success in encapsulating and differentiating human mesenchymal stem cells (hMSCs) toward an NP phenotype during hypoxic conditions. After demonstration of promising results in our previous work, in this study we have further investigated the inclusion of mechanical stimulation and its impact on hMSC differentiation toward an NP phenotype through the characterization of matrix markers such as SOX-9, aggrecan, and collagen II. Furthermore, investigations were undertaken in order to approximate delivery parameters for an injection delivery device, which could be used to transport hMSCs suspended in hydrogel into the IVD. hMSC-laden hydrogel solutions were injected through various needle gauge sizes in order to determine its impact on postinjection cell viability and IVD tissue penetration. Interpretation of these data informed the design of a potential minimally invasive injection device, which could successfully inject hMSCs encapsulated in a UV-curable polymer into NP, prior to photo-cross-linking in situ.

摘要

髓核(NP)组织损伤会对椎间盘(IVD)的生物力学性能产生有害的机械应变,导致随后的椎间盘退变。一种新型的、可光固化的、可注射的合成聚合物水凝胶(接枝有PAA的pHEMA-co-APMA)已在缺氧条件下成功地将人间充质干细胞(hMSCs)封装并诱导其向NP表型分化。在我们之前的工作取得了有前景的结果之后,在本研究中,我们通过对SOX-9、聚集蛋白聚糖和胶原蛋白II等基质标志物的表征,进一步研究了机械刺激的加入及其对hMSC向NP表型分化的影响。此外,还进行了研究以确定注射输送装置的近似输送参数,该装置可用于将悬浮在水凝胶中的hMSCs输送到IVD中。通过不同规格的针头注射负载hMSC的水凝胶溶液,以确定其对注射后细胞活力和IVD组织穿透的影响。对这些数据的解读为一种潜在的微创注射装置的设计提供了依据,该装置可以在原位光交联之前,成功地将封装在紫外线可固化聚合物中的hMSCs注射到NP中。

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