Oral Health Science Center HRC7, Tokyo Dental Collage, Chiba, Japan.
Int Endod J. 2010 Dec;43(12):1132-42. doi: 10.1111/j.1365-2591.2010.01789.x. Epub 2010 Oct 4.
To investigate the characteristics of side population (SP) cells derived from the dental pulp of young and aged rats.
Maxillary and mandibular incisors were extracted from 5-week-old (young) rats and 60- to 80-week-old (aged) rats. Coronal pulp tissue was removed mechanically, and single-cell suspensions were prepared using collagenase and dispase. Cells were stained with Hoechst 33342 and sorted with an fluorescence-activated cell sorter (FACS). Isolated SP and main population (MP) cells were analysed by real-time reverse transcription polymerase chain reaction, immunohistochemical localization and cell cycle determination. Two-way analysis of variance and the multiple comparison Scheffè test were used for statistical analysis (P<0.05).
Approximately 0.40% of pulp cells in young rats and 0.11% in aged rats comprised SP cells. SP cells expressed a higher mRNA level of ATP-binding cassette transporter G2 (ABCG2), but lower mRNA levels of nestin, alkaline phosphatase, p16 and p57 than MP cells in both age groups. Immunohistochemical observation revealed ABCG2-positive cells localized in the cell-rich zone and nestin in the odontoblastic layer in both groups. Furthermore, the majority of both young and aged SP and MP cells were in growth arrest of the G(0) /G(1) phase.
The FACS analysis revealed a decrease in the proportion of SP cells with age, whilst p16 mRNA expression indicated an increase in cell senescence. The cell cycles of SP and MP cells from both young and aged dental pulp were generally in the G0/G1 phase.
研究来自年轻和老年大鼠牙髓的侧群(SP)细胞的特征。
从 5 周龄(年轻)大鼠和 60-80 周龄(老年)大鼠中提取上颌和下颌切牙。通过机械方法去除冠状牙髓组织,并使用胶原酶和Dispase制备单细胞悬浮液。使用 Hoechst 33342 染色并用荧光激活细胞分选仪(FACS)进行分选。通过实时逆转录聚合酶链反应、免疫组织化学定位和细胞周期测定分析分离的 SP 和主群体(MP)细胞。采用双向方差分析和多重比较 Scheffè 检验进行统计学分析(P<0.05)。
年轻大鼠的牙髓细胞中约有 0.40%,老年大鼠中约有 0.11%为 SP 细胞。SP 细胞表达更高的 ATP 结合盒转运蛋白 G2(ABCG2)mRNA 水平,但在两组中均低于 MP 细胞的巢蛋白、碱性磷酸酶、p16 和 p57 mRNA 水平。免疫组织化学观察显示 ABCG2 阳性细胞在两组中均定位于细胞丰富区,巢蛋白位于成牙本质细胞层。此外,两组的年轻和老年 SP 和 MP 细胞的大部分均处于 G0/G1 期的生长停滞状态。
FACS 分析显示 SP 细胞的比例随年龄增长而减少,而 p16 mRNA 表达表明细胞衰老增加。来自年轻和老年牙髓的 SP 和 MP 细胞的细胞周期通常处于 G0/G1 期。