Matsumoto Yuji, Hof Akiko, Baumlin Yves, Müller Matthias, Prescott Margaret F, Hof Robert P
Novartis Institutes for BioMedical Research, Novartis Pharma AG, Basel, Switzerland.
Transplantation. 2003 Dec 15;76(11):1569-72. doi: 10.1097/01.TP.0000100686.06399.3A.
Recent observations have demonstrated the importance of host cells in neointima formation after transplantation. Because little is known regarding the dynamics of host-derived cells in the graft media, we investigated this question in a mouse carotid artery transplantation model.
C57BL/6 carotid arteries were orthotopically transplanted into BALB/c mice ubiquitously expressing enhanced green fluorescent protein. Grafts were harvested at 1, 2, 4, and 8 weeks after transplantation for histologic examination. No immunosuppression was used.
Immunostaining and semiquantitative analysis of cross sections showed that donor medial smooth muscle cells decreased over time in the graft media, whereas green fluorescent protein-positive/smooth muscle alpha-actin-positive cells (i.e., cells of host origin) increased over time. Interestingly, host cells were located only in the inner media and the neointima at 2 weeks and thereafter also in the outer media, indicating that the host-derived cells entered the media from the luminal side rather than from the adventitia. In longitudinal sections, there were no differences in the accumulation of donor- and host-derived cells between the end and middle regions of the graft media at 8 weeks.
After transplantation, medial cells were replaced by alpha-actin-expressing host cells that were probably derived from circulating precursor cells. Our observations differ from the traditional view of a major contribution of donor medial smooth muscle cells to the neointima formation. Thus, circulating progenitor cells may be important for graft vessel disease.
最近的观察结果表明宿主细胞在移植后新生内膜形成中具有重要作用。由于对移植血管中层中宿主来源细胞的动态变化了解甚少,我们在小鼠颈动脉移植模型中研究了这个问题。
将C57BL/6颈动脉原位移植到普遍表达增强型绿色荧光蛋白的BALB/c小鼠体内。在移植后1、2、4和8周采集移植血管进行组织学检查。未使用免疫抑制。
横断面的免疫染色和半定量分析显示,移植血管中层中供体平滑肌细胞随时间减少,而绿色荧光蛋白阳性/平滑肌α-肌动蛋白阳性细胞(即宿主来源的细胞)随时间增加。有趣的是,宿主细胞在2周时仅位于中层内侧和新生内膜,此后也出现在中层外侧,这表明宿主来源的细胞是从管腔侧而非外膜进入中层的。在纵断面中,移植血管中层末端和中间区域在8周时供体和宿主来源细胞的积累没有差异。
移植后,中层细胞被可能来源于循环前体细胞的表达α-肌动蛋白的宿主细胞所取代。我们的观察结果不同于传统观点,即供体中层平滑肌细胞对新生内膜形成起主要作用。因此,循环祖细胞可能对移植血管疾病很重要。