Li Pao, Gao Shang, Zhou Mei, Tang Hong, Mu Miduo, Zhang Jiqiang, Tang Kanglai
Department of Orthopedics, Orthopedic Center of Chinese PLA, Southwest Hospital, Third Military Medical University, Chongqing, 400038, P.R.China.
Department of Neurobiology, Third Military Medical University, Chongqing, 400038, P.R.China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2017 Apr 15;31(4):481-488. doi: 10.7507/1002-1892.201611102.
To investigate the effects of different mechanical stretch conditions on the differentiation of rat tendon stem cells (TSCs), to find the best uniaxial cyclic stretching for TSCs tenogenic differentiation, osteogenic differentiation, and adipogenic differentiation.
TSCs were isolated from the Achilles tendons of 8-week-old male Sprague Dawley rats by enzymatic digestion method and cultured. The TSCs at passage 3 were randomly divided into 5 groups: group A (stretch strength of 4% and frequency of 1 Hz), group B (stretch strength of 4% and frequency of 2 Hz), group C (stretch strength of 8% and frequency of 1 Hz), group D (stretch strength of 8% and frequency of 2 Hz), and group E (static culture). At 12, 24, and 48 hours after mechanical stretch, the mRNA expressions of the tenogenic differentiation related genes [Scleraxis (SCX) and Tenascin C (TNC)], the osteogenic differentiation related genes [runt related transcription factor 2 (RUNX2) and distal-less homeobox 5 (DLX5)], and the adipogenic differentiation related genes [CCAAT-enhancer-binding protein-α (CEBPα) and lipoprteinlipase (LPL)] were detected by real-time fluorescent quantitative PCR and the protein expressions of TNC, CEBPα, and RUNX2 were detected by Western blot.
The mRNA expressions of SCX and TNC in group B were significantly higher than those in groups A, C, D, and E at 24 hours after mechanical stretch ( <0.05). The mRNA expressions of CEBPα and LPL in group D were significantly higher than those in groups A, B, C, and E at 48 hours after mechanical stretch ( <0.05). The mRNA expressions of RUNX2 and DLX5 in group C were significantly higher than those in groups A, B, D, and E at 24 hours after mechanical stretch ( <0.05). Western blot detection showed that higher protein expression of TNC in group B than group E at each time point after mechanical stretch ( <0.05), and the protein expression of CEBPα was significantly inhibited when compared with group E at 24 hours after mechanical stretch ( <0.05). At 24 hours after mechanical stretch, the protein expression of RUNX2 in group C was significantly higher than that in group E ( <0.05); and the protein expression of TNC was significantly lower than that in group E at 24 and 48 hours after mechanical stretch ( <0.05). At 48 hours after mechanical stretch, the protein expression of CEBPα was significantly increased and the protein expression of TNC was significantly decreased in group D when compared with group E ( <0.05), but no significant difference was found in the protein expression of RUNX2 between groups D and E ( >0.05).
The mechanical strain could promote differentiation of TSCs, and different parameter of stretch will lead to different differentiation. The best stretch condition for tenogenic differentiation is 4% strength and 2 Hz frequency for 24 hours; the best stretch condition for osteogenic differentiation is 8% strength and 1 Hz frequency for 24 hours; and the best stretch condition for adipogenic differentiation is 8% strength and 2 Hz frequency for 48 hours.
研究不同机械拉伸条件对大鼠肌腱干细胞(TSCs)分化的影响,寻找TSCs向肌腱分化、成骨分化及成脂分化的最佳单轴循环拉伸条件。
采用酶消化法从8周龄雄性Sprague Dawley大鼠的跟腱中分离TSCs并进行培养。将第3代TSCs随机分为5组:A组(拉伸强度4%,频率1 Hz)、B组(拉伸强度4%,频率2 Hz)、C组(拉伸强度8%,频率1 Hz)、D组(拉伸强度8%,频率2 Hz)和E组(静态培养)。在机械拉伸后12、24和48小时,采用实时荧光定量PCR检测肌腱分化相关基因[硬骨素(SCX)和腱生蛋白C(TNC)]、成骨分化相关基因[ runt相关转录因子2(RUNX2)和远端缺失同源盒5(DLX5)]及成脂分化相关基因[CCAAT增强子结合蛋白α(CEBPα)和脂蛋白脂肪酶(LPL)]的mRNA表达,采用蛋白质免疫印迹法检测TNC、CEBPα和RUNX2的蛋白表达。
机械拉伸后24小时,B组SCX和TNC的mRNA表达显著高于A、C、D和E组(<0.05)。机械拉伸后48小时,D组CEBPα和LPL的mRNA表达显著高于A、B、C和E组(<0.05)。机械拉伸后24小时,C组RUNX2和DLX5的mRNA表达显著高于A、B、D和E组(<0.05)。蛋白质免疫印迹检测显示,机械拉伸后各时间点B组TNC蛋白表达均高于E组(<0.05),机械拉伸后24小时,CEBPα蛋白表达与E组相比显著受到抑制(<0.05)。机械拉伸后24小时,C组RUNX2蛋白表达显著高于E组(<0.05);机械拉伸后24和48小时,TNC蛋白表达显著低于E组(<0.05)。机械拉伸后48小时,D组CEBPα蛋白表达显著升高,TNC蛋白表达显著降低,与E组相比差异有统计学意义(<0.05),但D组和E组RUNX2蛋白表达差异无统计学意义(>0.05)。
机械应变可促进TSCs的分化,不同的拉伸参数会导致不同的分化结果。肌腱分化的最佳拉伸条件为强度4%、频率2 Hz、持续24小时;成骨分化的最佳拉伸条件为强度8%、频率1 Hz、持续24小时;成脂分化的最佳拉伸条件为强度8%、频率2 Hz、持续48小时。