Xu Lu, Zhou Jianjun, Liu Jingyu, Liu Yong, Wang Lei, Jiang Ruiwei, Diao Zhenyu, Yan Guijun, Pèault Bruno, Sun Haixiang, Ding Lijun
Center for Reproductive Medicine, Department of Obstetrics and Gynecology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, 321 Zhongshan Rd., Nanjing 210008, China.
Central Research Lab, The Affiliated Drum Tower Hospital of Nanjing University Medical School, 321 Zhongshan Rd., Nanjing 210008, China.
Stem Cells Int. 2017;2017:3175748. doi: 10.1155/2017/3175748. Epub 2017 Aug 10.
Human mesenchymal stem cells derived from the umbilical cord (UC) are a favorable source for allogeneic cell therapy. Here, we successfully isolated the stem cells derived from three different compartments of the human UC, including perivascular stem cells derived from umbilical arteries (UCA-PSCs), perivascular stem cells derived from umbilical vein (UCV-PSCs), and mesenchymal stem cells derived from Wharton's jelly (WJ-MSCs). These cells had the similar phenotype and differentiation potential toward adipocytes, osteoblasts, and neuron-like cells. However, UCA-PSCs and UCV-PSCs had more CD146 cells than WJ-MSCs ( < 0.05). Tube formation assay in vitro showed the largest number of tube-like structures and branch points in UCA-PSCs among the three stem cells. Additionally, the total tube length in UCA-PSCs and UCV-PSCs was significantly longer than in WJ-MSCs ( < 0.01). Microarray, qRT-PCR, and Western blot analysis showed that UCA-PSCs had the highest expression of the Notch ligand Jagged1 (JAG1), which is crucial for blood vessel maturation. Knockdown of Jagged1 significantly impaired the angiogenesis in UCA-PSCs. In summary, UCA-PSCs are promising cell populations for clinical use in ischemic diseases.
源自脐带(UC)的人间充质干细胞是同种异体细胞治疗的理想来源。在此,我们成功分离出源自人UC三个不同部位的干细胞,包括源自脐动脉的血管周围干细胞(UCA-PSC)、源自脐静脉的血管周围干细胞(UCV-PSC)以及源自华通氏胶的间充质干细胞(WJ-MSC)。这些细胞具有相似的表型以及向脂肪细胞、成骨细胞和神经元样细胞分化的潜能。然而,UCA-PSC和UCV-PSC中的CD146细胞比WJ-MSC更多(<0.05)。体外管形成试验显示,在这三种干细胞中,UCA-PSC形成的管状结构和分支点数量最多。此外,UCA-PSC和UCV-PSC中的总管长度显著长于WJ-MSC(<0.01)。基因芯片、定量逆转录-聚合酶链反应(qRT-PCR)和蛋白质免疫印迹分析表明,UCA-PSC中Notch配体Jagged1(JAG1)的表达最高,而JAG1对血管成熟至关重要。敲低Jagged1会显著损害UCA-PSC中的血管生成。总之,UCA-PSC是用于缺血性疾病临床治疗的有前景的细胞群体。