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. 2004 Sep 15;114(6):744–754. doi: 10.1172/JCI22991

Figure 4.

Figure 4

Illustration of two in vitro models for studying human cytotrophoblast invasion. (A) When human cytotrophoblasts (light green cells encircled in red) are isolated from early-gestation placentas and plated on an extracellular matrix (ECM) substrate (Matrigel), they differentiate along the pathway that leads to uterine invasion. By 12 hours in culture these cells form aggregates that resemble cell columns of anchoring villi, and by 48 hours they switch on expression of a repertoire of stage-specific antigens that are expressed in cytotrophoblasts within the uterine wall in situ (dark green cells). These molecules facilitate uterine invasion, vascular mimicry, and evasion of the maternal immune response. (B) When anchoring villi are dissected from the surfaces of early-gestation human placentas (blue box) and plated on an ECM substrate, cytotrophoblasts in cell columns continue to differentiate. By 48 hours many cytotrophoblasts have left the columns and invaded the substrate (green box). During this process they execute the same phenotypic switch that isolated cells carry out.