ESC, without a feeder layer--just media and LIF. And I'm not absolutely possitive, but none-the-less pretty sure, that we're NOT using phase contrast microscopes.
But I think you're on to something about the structural aspects... when the ES cells are attached to gelatin layer, their podia/podia-like extensions stop appearing "shiny"... so maybe its something specific to the z-axis structure.
More details on 'shiny': the perimeter of the cells have almost a white glow; a general brightness at their periphery.