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首页> 外文期刊>The Journal of heart and lung transplantation: the official publication of the International Society for Heart Transplantation >A novel sub-population of bone marrow-derived myocardial stem cells: potential autologous cell therapy in myocardial infarction.
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A novel sub-population of bone marrow-derived myocardial stem cells: potential autologous cell therapy in myocardial infarction.

机译:骨髓来源的心肌干细胞的新型亚群:心肌梗死的潜在自体细胞治疗。

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摘要

BACKGROUND: Several studies have identified beta2-microglobulin-negative (beta2M(-)) cells as a potential stem cell fraction in the bone marrow of rats and humans. We studied the ability of bone marrow-derived beta2M(-) cells to differentiate into cardiomyocytes and reconstitute the myocardium in a model of myocardial infarction. METHODS: beta2M(-) cells were purified from bone marrow of Lewis rats using a magnetic activated cell-sorting technique. beta2M(-) cells, 2.5 x 10(6) cells in 100 microl of phosphate-buffered saline (PBS), were transplanted 7 days after infarction into a transmural myocardial scar induced by cryoinjury in Lewis rats (n = 9). Control Group 1(n = 10) received a 100-microl injection of PBS, and Control Group 2 (n = 15) received no injection. The beta2M(-) cells were labeled before transplantation, using the membrane fluorescent intercalated dye, PKH26. Repopulation was examined at 6 and 8 weeks after transplantation. Differentiation of beta2M(-) cells into cardiac myocytes was determined by the colocalization of troponin and PKH26 to the same cell, utilizing immunohistochemistry, ultraviolet photomicroscopy and fluorescence microscopy on 6-microm serial sections. Area of engraftment within the scar was calculated by planimetry. RESULTS: The treatment group had multiple islands of de novo-formed myocardium within the fibrous matrix of the transmural scar (mean area 35 +/- 4.2% of scar area at 6 and 8 weeks). These cells colocalized cardiac-specific troponin and PKH26. Using these techniques, no myocardial islands were seen in the control groups. Before transplantation, beta2M(-) cells were troponin-negative. CONCLUSIONS: This study demonstrates that beta2M(-) cells represent a novel sub-population of bone marrow-derived stem cells capable of successful and substantial engraftment in areas of transmural myocardial scar, with de novo formation of cardiac myocytes. The functional significance of this observation is being studied.
机译:背景:几项研究已确定beta2微球蛋白阴性(beta2M(-))细胞作为大鼠和人类骨髓中的潜在干细胞部分。我们研究了在心肌梗死模型中骨髓来源的beta2M(-)细胞分化为心肌细胞和重构心肌的能力。方法:使用磁性激活细胞分选技术从Lewis大鼠的骨髓中纯化beta2M(-)细胞。在梗死后7天,将beta2M(-)细胞(100微升磷酸盐缓冲盐水(PBS)中的2.5 x 10(6)个细胞)移植到Lewis大鼠(n = 9)中,冷冻损伤引起的透壁心肌瘢痕中。对照组1(n = 10)接受100微升PBS注射,对照组2(n = 15)不接受注射。使用膜荧光嵌入染料PKH26在移植前标记beta2M(-)细胞。移植后第6和8周检查种群。通过将肌钙蛋白和PKH26共同定位到同一细胞,利用免疫组织化学,紫外光学显微镜和荧光显微镜对6微米系列切片进行检测,确定了beta2M(-)细胞向心肌细胞的分化。通过平面测量法计算疤痕内的植入面积。结果:治疗组在透壁瘢痕的纤维基质内有多个从头形成的心肌岛(在第6和第8周,平均面积为瘢痕面积的35 +/- 4.2%)。这些细胞共定位心脏特异性肌钙蛋白和PKH26。使用这些技术,对照组中未见心肌岛。移植前,beta2M(-)细胞是肌钙蛋白阴性的。结论:这项研究表明,beta2M(-)细胞代表一种新型的骨髓来源的干细胞亚群,能够成功并大量植入透壁心肌瘢痕区域,并从头形成心肌细胞。正在研究此观察的功能意义。

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