Golat Brian T, Cameron Don F
Department of Pathology & Cell Biology, College of Medicine, University of South Florida, Tampa, FL 33612, USA.
Cell Transplant. 2008;17(10-11):1135-44. doi: 10.3727/096368908787236512.
Sertoli cells isolated from the testis (referred to as extratesticular Sertoli cells) have been shown to facilitate allo- and xenogeneic cell transplantations. It appears likely that the ability of these cells to enhance the success of cell engraftment is due, in part, to the retention of their intratesticular functions of trophic support and immunoprotection. Sertoli cells also are involved in the regulation of angiogenesis in the testis, which may also contribute to enhanced cell engraftment success facilitated by extratesticular Sertoli cells. Because the maintenance of the cell's intratesticular angiogenic function has not yet been evaluated for extratesticular Sertoli cells, this study examined the cell's ability to enhance angiogenesis in vitro. Sertoli cell conditioned media were derived from isolated rat Sertoli cell cultures and used in a rat aortic model of induced angiogenesis, in endothelial and smooth muscle cell monocultures, and in endothelial smooth muscle cocultures. An angiogenic rat cytokine array identified angiogenic factors in the control and conditioned media. Aorta sections incubated with Sertoli cell conditioned media showed a marked increase in the formation of capillary-like structures when compared to controls. Likewise, endothelial cells incubated in conditioned media organized into capillary-like structures not observed when incubated in control media. In coculture, smooth muscle cells were associated with endothelial cell-derived capillary-like structures only when incubated in conditioned media. Cytokine arrays indicated the presence and a qualitative increase of specific angiogenic growth factors in Sertoli cell conditioned media not observed in control media. Results indicate that extratesticular Sertoli cells retain their intratesticular angiogenic function in vitro.
从睾丸分离出的支持细胞(称为睾丸外支持细胞)已被证明有助于同种异体和异种细胞移植。这些细胞增强细胞植入成功率的能力,似乎部分归因于它们保留了睾丸内的营养支持和免疫保护功能。支持细胞还参与睾丸血管生成的调节,这也可能有助于提高睾丸外支持细胞促进的细胞植入成功率。由于尚未评估睾丸外支持细胞维持其睾丸内血管生成功能的情况,本研究检测了这些细胞在体外增强血管生成的能力。支持细胞条件培养基取自分离的大鼠支持细胞培养物,并用于诱导血管生成的大鼠主动脉模型、内皮细胞和平滑肌细胞单培养以及内皮-平滑肌共培养。一种血管生成大鼠细胞因子阵列鉴定了对照培养基和条件培养基中的血管生成因子。与对照相比,用支持细胞条件培养基孵育的主动脉切片显示毛细血管样结构的形成显著增加。同样,在条件培养基中孵育的内皮细胞组织成在对照培养基中孵育时未观察到的毛细血管样结构。在共培养中,只有在条件培养基中孵育时,平滑肌细胞才与内皮细胞衍生的毛细血管样结构相关。细胞因子阵列表明,支持细胞条件培养基中存在特定的血管生成生长因子,且与对照培养基相比有定性增加。结果表明,睾丸外支持细胞在体外保留了其睾丸内的血管生成功能。