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PRIMORDIAL GERM CELL‐DERIVED MOUSE EMBRYONIC GERM (EG) CELLS IN VITRO RESEMBLE UNDIFFERENTIATED STEM CELLS WITH RESPECT TO DIFFERENTIATION CAPACITY AND CELL CYCLE DISTRIBUTION
Author(s) -
ROHWEDEL JÜRGEN,
SEHLMEYER ULRICH,
SHAN JIN,
MEISTER ARMIN,
WOBUS ANNA M.
Publication year - 1996
Publication title -
cell biology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.932
H-Index - 77
eISSN - 1095-8355
pISSN - 1065-6995
DOI - 10.1006/cbir.1996.0076
Subject(s) - p19 cell , biology , embryonic stem cell , cellular differentiation , embryoid body , microbiology and biotechnology , stem cell , adult stem cell , somatic cell , cell cycle , totipotent , cell culture , flow cytometry , cell , genetics , gene
Embryonic germ (EG) cells of line EG‐1 derived from mouse primordial germ cells were investigated for their in vitro differentiation capacity. By cultivation as embryo‐like aggregates EG‐1 cells differentiated into cardiac, skeletal muscle and neuronal cells accompanied by the expression of tissue‐specific genes and proteins as shown by RT‐PCR analysis and indirect immunofluorescence. In comparison to embryonic stem (ES) cells of line D3 the efficiency of differentiation into cardiac and muscle cells was comparatively low, whereas spontaneous neuronal differentiation was more efficient than in D3 cells. Furthermore, the distribution of cell cycle phases as a parameter for the differentiation state was analysed in undifferentiated EG cells and ES cells and compared to data obtained for embryonic carcinoma (EC) cells of line P19 and differentiated, epithelioid EPI‐7 cells. Flow cytometric analysis revealed similar cell cycle phase distributions in EG, EC and ES cells. In contrast, the somatic differentiated EPI‐7 cells showed a longer G 1 ‐phase and shorter S‐ and G 2 /M‐phases. Together, our results demonstrate that the differentiation state and capacity of EG cells in vitro resemble that of totipotent ES cells.