Dudakovic Amel, Camilleri Emily, Riester Scott M, Lewallen Eric A, Kvasha Sergiy, Chen Xiaoyue, Radel Darcie J, Anderson Jarett M, Nair Asha A, Evans Jared M, Krych Aaron J, Smith Jay, Deyle David R, Stein Janet L, Stein Gary S, Im Hee-Jeong, Cool Simon M, Westendorf Jennifer J, Kakar Sanjeev, Dietz Allan B, van Wijnen Andre J
Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota.
J Cell Biochem. 2014 Oct;115(10):1816-28. doi: 10.1002/jcb.24852.
Improving the effectiveness of adipose-tissue derived human mesenchymal stromal/stem cells (AMSCs) for skeletal therapies requires a detailed characterization of mechanisms supporting cell proliferation and multi-potency. We investigated the molecular phenotype of AMSCs that were either actively proliferating in platelet lysate or in a basal non-proliferative state. Flow cytometry combined with high-throughput RNA sequencing (RNASeq) and RT-qPCR analyses validate that AMSCs express classic mesenchymal cell surface markers (e.g., CD44, CD73/NT5E, CD90/THY1, and CD105/ENG). Expression of CD90 is selectively elevated at confluence. Self-renewing AMSCs express a standard cell cycle program that successively mediates DNA replication, chromatin packaging, cyto-architectural enlargement, and mitotic division. Confluent AMSCs preferentially express genes involved in extracellular matrix (ECM) formation and cellular communication. For example, cell cycle-related biomarkers (e.g., cyclins E2 and B2, transcription factor E2F1) and histone-related genes (e.g., H4, HINFP, NPAT) are elevated in proliferating AMSCs, while ECM genes are strongly upregulated (>10-fold) in quiescent AMSCs. AMSCs also express pluripotency genes (e.g., POU5F1, NANOG, KLF4) and early mesenchymal markers (e.g., NES, ACTA2) consistent with their multipotent phenotype. Strikingly, AMSCs modulate expression of WNT signaling components and switch production of WNT ligands (from WNT5A/WNT5B/WNT7B to WNT2/WNT2B), while upregulating WNT-related genes (WISP2, SFRP2, and SFRP4). Furthermore, post-proliferative AMSCs spontaneously express fibroblastic, osteogenic, chondrogenic, and adipogenic biomarkers when maintained in confluent cultures. Our findings validate the biological properties of self-renewing and multi-potent AMSCs by providing high-resolution quality control data that support their clinical versatility.
提高脂肪组织来源的人间充质基质/干细胞(AMSCs)用于骨骼治疗的有效性,需要详细了解支持细胞增殖和多能性的机制。我们研究了在血小板裂解物中活跃增殖或处于基础非增殖状态的AMSCs的分子表型。流式细胞术结合高通量RNA测序(RNASeq)和RT-qPCR分析证实,AMSCs表达经典的间充质细胞表面标志物(如CD44、CD73/NT5E、CD90/THY1和CD105/ENG)。CD90的表达在汇合时选择性升高。自我更新的AMSCs表达一个标准的细胞周期程序,该程序依次介导DNA复制、染色质包装、细胞结构扩大和有丝分裂。汇合的AMSCs优先表达参与细胞外基质(ECM)形成和细胞通讯的基因。例如,细胞周期相关生物标志物(如细胞周期蛋白E2和B2、转录因子E2F1)和组蛋白相关基因(如H4、HINFP、NPAT)在增殖的AMSCs中升高,而ECM基因在静止的AMSCs中强烈上调(>10倍)。AMSCs还表达多能性基因(如POU5F1、NANOG、KLF4)和早期间充质标志物(如NES、ACTA2),与其多能表型一致。引人注目的是,AMSCs调节WNT信号成分的表达并切换WNT配体的产生(从WNT5A/WNT5B/WNT7B切换到WNT2/WNT2B),同时上调WNT相关基因(WISP2、SFRP2和SFRP4)。此外,增殖后的AMSCs在汇合培养时自发表达成纤维细胞、成骨细胞、软骨细胞和脂肪生成生物标志物。我们的研究结果通过提供支持其临床多功能性的高分辨率质量控制数据,验证了自我更新和多能AMSCs的生物学特性。