Dvorakova Jana, Velebny Vladimir, Kubala Lukas
CPN s.r.o, Dolní Dobrouc, Czech Republic.
Neuro Endocrinol Lett. 2008 Oct;29(5):685-90.
Hyaluronan (HA) is an abundant component of chondrogenic tissue hence it is often used as a fundamental constituent in cartilage tissue substitutes. However, effects of different molecular weight HA on chondrogenic differentiation are not clear. The aim was to evaluate modulation of mesenchymal stem cell (MSC) early chondrogenesis by HA of molecular weights 100, 600 and 1 500 kDa.
HA was applied on MSCs cultured in a pellet system for one, two and three weeks. Chondrogenesis was evaluated by determinations of gene expression of transcription factor Sox-9 and extracellular matrix proteins collagen type II and XI, aggrecan, and COMP by Real-Time PCR and completed with histological analysis.
Upon chondrogenic induction, the respective pellets revealed active transcription of the chondrogenic genes together with proceeding accumulation of glycosaminoglycan (GAG) rich extracellular matrix. Sox-9 was also expressed in non-chondrogenic MSC controls. HA treated pellets were not significantly influenced on day 7 of culture. However, on day 14, lowered expression in some of the extracellular matrix proteins appeared together with a moderately smaller amount of GAG content in pellet sections. Nevertheless, the analysis on day 21 has demonstrated that HA did not affect the outcome of the differentiation by the end of the culture. Any difference regarding the molecular weight of the HA was not found.
It could be speculated that HA induced a time shift in the phase of the dominant matrix protein onset which was in full compensated by the end of the evaluated time period. Thus, data suggest that HA of any tested molecular weight does not significantly modulate chondrogenesis of MSCs in pellet system.
透明质酸(HA)是软骨组织的一种丰富成分,因此它常被用作软骨组织替代物的基本成分。然而,不同分子量的HA对软骨形成分化的影响尚不清楚。本研究旨在评估分子量为100、600和1500 kDa的HA对间充质干细胞(MSC)早期软骨形成的调节作用。
将HA应用于在微团培养系统中培养1、2和3周的MSC。通过实时定量PCR测定转录因子Sox-9以及细胞外基质蛋白II型和XI型胶原蛋白、聚集蛋白聚糖和软骨寡聚基质蛋白的基因表达来评估软骨形成,并进行组织学分析。
在软骨形成诱导后,各个微团显示软骨形成基因的活跃转录以及富含糖胺聚糖(GAG)的细胞外基质的持续积累。Sox-9在非软骨形成的MSC对照中也有表达。在培养第7天时,HA处理组微团未受到显著影响。然而,在第14天时,一些细胞外基质蛋白的表达降低,同时微团切片中GAG含量略有减少。尽管如此,第21天的分析表明,在培养结束时HA并未影响分化结果。未发现HA分子量之间存在任何差异。
可以推测,HA诱导了主要基质蛋白出现阶段的时间变化,而在评估时间段结束时这种变化得到了完全补偿。因此,数据表明,在微团培养系统中,任何测试分子量的HA均不会显著调节MSC的软骨形成。