Jackson L, Gibas L M, Barr M A
Jefferson Medical College, Philadelphia, Pennsylvania, USA.
Curr Protoc Hum Genet. 2001 May;Chapter 8:Unit 8.3. doi: 10.1002/0471142905.hg0803s00.
Chorionic villi are composed of an outer layer of trophoblastic cells and an inner mesenchymal cell core, both of fetal origin. Cytogenetic analysis of chorionic villi can be accomplished using material prepared in either of two ways. In the culture method described in this unit, villi are disaggregated by mechanical and enzymatic methods, and the resulting cell suspension is used to establish primary cultures. Mesenchymal cells of the villus core are released by this procedure and the fibroblasts are actively proliferative in tissue culture. Cultures can be used for cytogenetic analysis after 1 week. In the "direct" technique, presented here in an Alternate Protocol, Langhans cells of the cytotrophoblast, actively dividing cells in first-trimester villi, are synchronized and arrested in mitosis after a short incubation period, and metaphase spreads are prepared. Chorionic villi are composed of an outer layer of trophoblastic cells and an inner mesenchymal cell core, both of fetal origin.
绒毛膜绒毛由外层滋养层细胞和内层间充质细胞核心组成,二者均来源于胎儿。绒毛膜绒毛的细胞遗传学分析可以使用两种方法之一制备的材料来完成。在本单元所述的培养方法中,通过机械和酶促方法将绒毛解离,所得细胞悬液用于建立原代培养。通过该程序可释放绒毛核心的间充质细胞,并且成纤维细胞在组织培养中具有活跃的增殖能力。培养1周后可用于细胞遗传学分析。在“直接”技术(此处以替代方案呈现)中,细胞滋养层的朗汉斯细胞(孕早期绒毛中活跃分裂的细胞)在短时间孵育后同步化并停滞在有丝分裂期,然后制备中期染色体铺片。绒毛膜绒毛由外层滋养层细胞和内层间充质细胞核心组成,二者均来源于胎儿。