Jia Jun, Huang Xin, Zhang Wen-Feng, Zhao Yi-Fang
Key Laboratory of Oral Biomedical Engineering, Ministry of Education (KLOBM), Wuhan University, Wuhan 430079, China.
Cardiovasc Pathol. 2008 Jul-Aug;17(4):212-8. doi: 10.1016/j.carpath.2007.09.003. Epub 2007 Nov 28.
Hemangiomas are highly prevalent in newborns and infants and can lead to severe complications. However, the pathogenesis of hemangiomas is still unknown. This study was designed to examine the potential of human monocytes to differentiate into hemangioma endothelial cells.
Purified monocytes from adult human peripheral blood were cultured under a conditional culture environment supplemented with basic fibroblast growth factor and vascular endothelial growth factor. Cells cultured for 2 weeks were subjected to histological and immunochemical examinations in order to determine the expression of specific markers for hemangioma endothelial cells.
Monocytes cultured for 2 weeks in angiogenic medium expressed human erythrocyte-type glucose transporter protein, FcgammaRII, and several other endothelial markers, all of which are deemed specific markers for hemangioma endothelial cells. However, neither CD133 nor alpha smooth muscle actin was detected in our monocyte culture.
Our data suggested that monocytes are capable of differentiating into hemangioma endothelial cells under the angiogenic stimulation from microenvironment of proliferative hemangioma.
血管瘤在新生儿和婴儿中非常普遍,可导致严重并发症。然而,血管瘤的发病机制仍不清楚。本研究旨在探讨人类单核细胞分化为血管瘤内皮细胞的潜力。
从成人外周血中纯化的单核细胞在补充有碱性成纤维细胞生长因子和血管内皮生长因子的条件培养环境中培养。对培养2周的细胞进行组织学和免疫化学检查,以确定血管瘤内皮细胞特异性标志物的表达。
在血管生成培养基中培养2周的单核细胞表达人类红细胞型葡萄糖转运蛋白、FcγRII和其他几种内皮标志物,所有这些都被认为是血管瘤内皮细胞的特异性标志物。然而,在我们的单核细胞培养物中未检测到CD133和α平滑肌肌动蛋白。
我们的数据表明,在增殖性血管瘤微环境的血管生成刺激下,单核细胞能够分化为血管瘤内皮细胞。