1 Orthopaedic Biomechanics, Department of Biomedical Engineering, and Institute for Complex Molecular Systems, Eindhoven University of Technology , Eindhoven, The Netherlands .
2 Department of Clinical Sciences of Companion Animals, Faculty of Veterinary Medicine, Utrecht University , Utrecht, The Netherlands .
Tissue Eng Part A. 2016 Jan;22(1-2):103-10. doi: 10.1089/ten.TEA.2015.0121. Epub 2015 Nov 5.
Notochordal cell-conditioned medium (NCCM) has previously shown to have a stimulatory effect on nucleus pulposus cells (NPCs) and bone marrow stromal cells (BMSCs) in alginate and pellet cultures. These culture methods provide a different environment than the nucleus pulposus (NP) tissue, in which the NCCM ultimately should exert its effect. The objective of this study is to test whether NCCM stimulates NPCs within their native environment, and whether combined stimulation with NCCM and addition of BMSCs has a synergistic effect on extracellular matrix production.
Bovine NP tissue was cultured in an artificial annulus in base medium (BM), porcine NCCM, or BM supplemented with 1 μg/mL Link N. Furthermore, BM and NCCM samples were injected with 10(6) BMSCs per NP sample. Samples were cultured for 4 weeks, and analyzed for biochemical contents (water, glycosaminoglycan [GAG], hydroxyproline, and DNA), gene expression (COL1A1, COL2A1, ACAN, and SOX9), and histology by Safranin O/Fast Green staining.
Culture in NCCM resulted in increased proteoglycan content compared to day 0 and BM, similar to Link N. However, only minor differences in gene expression compared to day 0 were observed. Addition of BMSCs did not result in increased GAG content, and surprisingly, DNA content in BMSC-injected groups was not higher than in the other groups after 4 weeks of culture.
This study shows that, indeed, NCCM is capable of stimulating NPC matrix production within the NP environment. The lack of increased DNA content in the BMSC-injected groups indicates that BMSCs have died over time. Identification of the bioactive factors in NCCM is crucial for further development of an NCCM-based treatment for intervertebral disc regeneration.
脊索细胞条件培养基(NCCM)先前已显示出在藻酸盐和微球培养中对髓核细胞(NPC)和骨髓基质细胞(BMSC)具有刺激作用。这些培养方法提供了与髓核组织(NP)不同的环境,NCCM 最终应在该环境中发挥作用。本研究的目的是测试 NCCM 是否刺激 NPC 处于其天然环境中,以及 NCCM 与 BMSC 联合刺激是否对细胞外基质的产生具有协同作用。
将牛 NP 组织在基础培养基(BM)、猪 NCCM 或补充有 1μg/mL Link N 的 BM 中在人工环中培养。此外,将 BM 和 NCCM 样品分别注射到每个 NP 样品中 10^6^个 BMSC。培养 4 周后,通过番红 O/快绿染色对样品进行生化含量(水、糖胺聚糖[GAG]、羟脯氨酸和 DNA)、基因表达(COL1A1、COL2A1、ACAN 和 SOX9)和组织学分析。
与第 0 天和 BM 相比,NCCM 培养导致蛋白聚糖含量增加,与 Link N 相似。然而,与第 0 天相比,仅观察到基因表达的微小差异。添加 BMSC 并未导致 GAG 含量增加,令人惊讶的是,在培养 4 周后,BMSC 注射组的 DNA 含量并未高于其他组。
本研究表明,NCCM 确实能够在 NP 环境中刺激 NPC 基质的产生。BMSC 注射组中 DNA 含量没有增加表明 BMSC 随时间死亡。鉴定 NCCM 中的生物活性因子对于进一步开发基于 NCCM 的椎间盘再生治疗方法至关重要。