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模拟生理负荷下有限营养对原位椎间盘细胞的影响。

Effect of limited nutrition on in situ intervertebral disc cells under simulated-physiological loading.

作者信息

Jünger Svenja, Gantenbein-Ritter Benjamin, Lezuo Patrick, Alini Mauro, Ferguson Stephen J, Ito Keita

机构信息

AO Research Institute, Davos, Switzerland.

出版信息

Spine (Phila Pa 1976). 2009 May 20;34(12):1264-71. doi: 10.1097/BRS.0b013e3181a0193d.

Abstract

STUDY DESIGN

Whole ovine caudal intervertebral discs (IVD) were cultured in sufficient and limited nutrition under simulated-physiologic loading for 7 and 21 days.

OBJECTIVE

To study the effect of limited nutrition on disc cells embedded in their native tissue in short- and midterm whole organ disc culture.

SUMMARY OF BACKGROUND DATA

Nutrient-limited induction of disc cell death in vitro has been demonstrated and is believed to be a factor in disc degeneration. Nutrient-limited cell death and its consequences, as it relates to degeneration, have not been investigated in the intact IVD.

METHODS

Ovine IVDs with endplates were cultured for 7 and 21 days under simulated-physiologic loading, either in media with limited (2 g/L) or sufficient (4.5 g/L) glucose concentration. Cell viability, relative gene expression, newly synthesized chondroitin sulfate content, and matrix metalloproteinase (MMP) activity were measured after culture and compared to fresh tissue.

RESULTS

In sufficient glucose media, cell viability was maintained through 7 days to 21 days of culture. In limited glucose, it dropped significantly to 62% in the anulus fibrosus and to 56% in the nucleus pulposus after 7 days and remained so until 21 days (63% in the anulus fibrosus and 52% in the nucleus pulposus). No significant differences were found between culture conditions for relative gene expression, newly synthesized chondroitin sulfate and inactive and active forms of MMP13 and MMP7.

CONCLUSION

With this culture system, whole IVD explants could be maintained up to 21 days. Cell viability decreased to 50% to 60% under limited nutrition within days and remained so up to 3 weeks. The surviving cells did not compensate matrix production in this time frame.

摘要

研究设计

将完整的绵羊尾椎椎间盘(IVD)在模拟生理负荷下于充足营养和有限营养条件下培养7天和21天。

目的

研究在短期和中期全器官椎间盘培养中,有限营养对嵌入其天然组织中的椎间盘细胞的影响。

背景数据总结

体外已证实营养受限可诱导椎间盘细胞死亡,且被认为是椎间盘退变的一个因素。营养受限的细胞死亡及其与退变相关的后果,尚未在完整的椎间盘内进行研究。

方法

将带有终板的绵羊椎间盘在模拟生理负荷下培养7天和21天,培养基中葡萄糖浓度分别为有限(2g/L)或充足(4.5g/L)。培养后测量细胞活力、相对基因表达、新合成的硫酸软骨素含量和基质金属蛋白酶(MMP)活性,并与新鲜组织进行比较。

结果

在葡萄糖充足的培养基中,细胞活力在培养7天至21天期间得以维持。在葡萄糖有限的情况下,7天后纤维环中的细胞活力显著下降至62%,髓核中的细胞活力下降至56%,并一直维持到21天(纤维环中为63%,髓核中为52%)。在相对基因表达、新合成的硫酸软骨素以及MMP13和MMP7的无活性和活性形式方面,培养条件之间未发现显著差异。

结论

采用该培养系统,完整的椎间盘外植体可维持长达21天。在有限营养条件下,细胞活力在数天内降至50%至60%,并在长达3周的时间内保持这一水平。在此时间段内,存活细胞无法补偿基质产生。

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