DNA Synthesis Is Required for Reprogramming Mediated by Stem Cell Fusion
Author(s) -
Tomomi Tsubouchi,
Jorge Soza-Ried,
Karen Brown,
Francesco M. Piccolo,
Irene Cantone,
David Landeira,
Hakan Bagci,
Helfrid Hochegger,
Matthias Merkenschlager,
Amanda G. Fisher
Publication year - 2013
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2013.01.012
Subject(s) - reprogramming , biology , somatic cell , heterokaryon , embryonic stem cell , induced pluripotent stem cell , microbiology and biotechnology , cell fusion , genetics , cell , gene , mutant
Embryonic stem cells (ESCs) can instruct the conversion of differentiated cells toward pluripotency following cell-to-cell fusion by a mechanism that is rapid but poorly understood. Here, we used centrifugal elutriation to enrich for mouse ESCs at sequential stages of the cell cycle and showed that ESCs in S/G2 phases have an enhanced capacity to dominantly reprogram lymphocytes and fibroblasts in heterokaryon and hybrid assays. Reprogramming success was associated with an ability to induce precocious nucleotide incorporation within the somatic partner nuclei in heterokaryons. BrdU pulse-labeling experiments revealed that virtually all successfully reprogrammed somatic nuclei, identified on the basis of Oct4 re-expression, had undergone DNA synthesis within 24 hr of fusion with ESCs. This was essential for successful reprogramming because drugs that inhibited DNA polymerase activity effectively blocked pluripotent conversion. These data indicate that nucleotide incorporation is an early and critical event in the epigenetic reprogramming of somatic cells in experimental ESC-heterokaryons.
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