Abstract: The present invention provides methods for inducing the differentiation of pluripotent cells. The present inventors succeeded in differentiating hepatocytes from ES cells without EB formation, using simple adherent monoculturing in media comprising several growth factors in culture dishes with two different matrices.

Abstract: A solution temperature control device in a biological cell observing chamber (30) used for the detection of chemotaxis and chemotactic cell separator, comprising a first temperature controller (62) and a second temperature controller (63). The first temperature controller (62) measures the temperature of a solution filled in a pair of wells and a flow passage in the chamber and controls the temperature to a specified temperature, and the second temperature controller (63) measures the temperature of a heating part (64) which heats the chamber (30) from the outside to indirectly heat the solution filled in the pair of wells and the flow passage and controls the temperature to a specified preheat temperature. Since the state and quantity of cells moving from one well to the other through the flow passage while holding the temperature of the solution at a specified temperature can be accurately observed and measured, accuracy for controlling the temperature of the solution can be remarkably increased.

Abstract: A biological cell observing chamber (30), wherein an intermediate support body (32) forming a skeleton outer shell structural part is mounted on a bottom support body (31) and a cover block body (33) is mounted on the bottom support body (31) on which the intermediate support body (32) is mounted by using lever mechanisms (36) and (37) incorporating a cam mechanism and a clamp mechanism so that the contact faces thereof can be pressed against each other in the vertical direction. The cam mechanism comprises cam grooves (36b) and (37b) formed in both leg part inner surfaces of U-shaped levers (36) and (37) rotatably supported on the bottom support body (31) and pins (40) and (41) slidably moving in the cam grooves and built in the outer peripheral surfaces of the intermediate support body (32) and the cover block body (33) at corresponding two points.

Abstract: A disk for storing liquid samples containing cells and for use in counting and observing the cells through an optical microscope includes an upper member formed of a transparent material and having a plurality of liquid inlets arranged radially and adapted to introduce the corresponding liquid samples therethrough, and a plurality of air vents paired with the corresponding liquid inlets; an intermediate member having a plurality of chambers arranged radially and adapted to store the corresponding liquid samples therein, each chamber corresponding to each pair of the liquid inlet and the air vent and communicating with the liquid inlet and with the air vent; and a lower member formed of a transparent material and backing the intermediate member. The optical microscope assumes the form of an incident-light microscope.

Abstract: There is provided cell observation apparatus (10) comprising cell observation chamber (30) and optical observation means (70), the cell observation chamber (30) having, disposed thereinside, a pair of wells and a channel through which the wells communicate with each other so that cells of a cell suspension stocked in one of the pair of wells can react with a chemotaxis-factor-containing solution stocked in the other well and can move from the one well to the other well through the channel, the optical observation means (70) capable of optically observing the cells moving through the channel from outside of the cell observation chamber (30), wherein the cell observation chamber (30) with its part exposed from casing (20) is housed in the casing (20) and wherein the optical observation means (70) is housed in the casing (20) so that the optical axis thereof horizontally extends alow in the cell observation chamber (30).

Abstract: The present invention provides modified methods of producing human hepatocyte-like cells which exhibit phenotypes more similar to those of human hepatocytes. The present invention also provides the human hepatocyte-like cells and uses thereof. The methods of the present invention comprises a prolonged incubation period and addition of dexamethasone to the culture medium. The methods of the inventors produce human hepatocyte-like cells whose morphology is more similar to that of human hepatocytes, compared with the conventional system. The cells produced have both morphological and functional features of primary culture cells from normal human liver, including cytochrome P450 (CYP), multi-drug resistance-associated protein (MRP), and multi-drug protein (MDR).