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人椎间盘髓核细胞在海藻酸盐和壳聚糖-明胶支架中的特性测定与比较

Determination and comparison of specifics of nucleus pulposus cells of human intervertebral disc in alginate and chitosan-gelatin scaffolds.

作者信息

Renani Hamid Bahramian, Ghorbani Masood, Beni Batool Hashemibeni, Karimi Z, Mirhosseini Mm, Zarkesh H, Kabiri A

机构信息

Department of Anatomy and Molecular Biology, School of Medicine, Isfahan, Iran.

出版信息

Adv Biomed Res. 2012;1:81. doi: 10.4103/2277-9175.102996. Epub 2012 Oct 31.

Abstract

INTRODUCTION

Low back pain is a major economical and social problem nowadays. Intervertebral disc herniation and central degeneration of disc are two major reasons of low back pain that occur because of structural impairment of disc. The intervertebral disc contains three parts as follows : Annulus fibrosus, transitional region, and nucleus pulposus, which forms the central nucleus of the disc. The reduction of cell count and extracellular matrix, especially in nucleus pulposus, causes disc degeneration. Different scaffolds (natural and synthetic) have been used for tissue repairing and regeneration of the intervertebral disc in tissue engineering. Most scaffolds have biodegradable and biocompatible characteristics and also prepare a fine condition for proliferation and migration of cells. In this study, proliferation of NP cells of human intervertebral disc compromised in Chitosan-gelatin scaffold with alginate scaffold was studied.

MATERIALS AND METHODS

NP cells derived from nucleus pulposus by collagenase enzymatic hydrolysis. They were derived from patients who undergoing open surgery for discectomy in the Isfahan Alzahra hospital. Chitosan was blended with gelatin and glutaraldehyde was used for cross linking the two polymers. Then, alginate scaffold was prepared. Cellular suspension with 1 × 10(5) transferred to each scaffold and cultured for 21 days. Cell viability and proliferation investigated by trypan blue and (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Scanning electron microscope (SEM) was used to assert the porosity and to survey structure of scaffold.

RESULTS

MTT assay dem1onstrated that cell viability of third day had significant difference in contrast by first day in both scaffolds. Accordingly, there was a significant decreased in cellular viability from day 3 to 21. Results of the cell count showed a punctual elevation cell numbers for alginate scaffold but there was no similar result for chitosan-gelatin scaffold.

CONCLUSION

Alginate scaffold prepared a better condition for proliferation of NP cells in comparison with chitosan-gelatin scaffold. Results of this study suggest that alginate scaffold could be useful in in vivo studies and treatment.

摘要

引言

如今,腰痛是一个重大的经济和社会问题。椎间盘突出和椎间盘中央退变是由于椎间盘结构损伤而导致腰痛的两个主要原因。椎间盘包含以下三个部分:纤维环、过渡区和髓核,髓核构成椎间盘的中央核心。细胞数量和细胞外基质的减少,尤其是在髓核中,会导致椎间盘退变。在组织工程中,不同的支架(天然和合成的)已被用于椎间盘的组织修复和再生。大多数支架具有可生物降解和生物相容性的特性,并且还为细胞的增殖和迁移创造了良好的条件。在本研究中,研究了壳聚糖 - 明胶支架与海藻酸盐支架对人椎间盘髓核细胞增殖的影响。

材料与方法

通过胶原酶酶解从髓核中获取髓核细胞。这些细胞来自在伊斯法罕阿尔扎赫拉医院接受开放性椎间盘切除术的患者。将壳聚糖与明胶混合,并用戊二醛交联这两种聚合物。然后,制备海藻酸盐支架。将含有1×10⁵个细胞的细胞悬液转移到每个支架中,并培养21天。通过台盼蓝和(3 -(4,5 - 二甲基噻唑 - 2 - 基)- 2,5 - 二苯基四氮唑溴盐(MTT)法研究细胞活力和增殖情况。使用扫描电子显微镜(SEM)来确定支架的孔隙率并观察支架结构。

结果

MTT分析表明,在两种支架中,第3天的细胞活力与第1天相比有显著差异。因此,从第3天到第21天,细胞活力显著下降。细胞计数结果显示海藻酸盐支架的细胞数量有短暂升高,但壳聚糖 - 明胶支架没有类似结果。

结论

与壳聚糖 - 明胶支架相比,海藻酸盐支架为髓核细胞的增殖创造了更好的条件。本研究结果表明,海藻酸盐支架可能在体内研究和治疗中有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c84d/3544085/afca8330aca0/ABR-1-81-g001.jpg

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