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Stem Cells 2004;22:883-889 www.StemCells.com
© 2004 AlphaMed Press


RAPID COMMUNICATION

Presence of Functional Gap Junctions in Human Embryonic Stem Cells

Raymond C.B. Wong, Alice Pébay, Linh T.V. Nguyen, Karen L.L. Koh, Martin F. Pera

Monash Institute of Reproduction and Development, Monash University, Clayton,Australia

Key Words. Human embryonic stem cells • Gap junction • Connexin 43 • Connexin 45

Correspondence: Dr. A. Pébay, Ph.D., Monash Institute of Reproduction and Development, Monash University, 246 Clayton Road, Clayton, VIC 3168,Australia. Telephone: 0061-395947302; Fax: 0061-95947311, e-mail: alice.pebay{at}med.monash.edu.au

Gap junctions are intercellular channels that allow both chemical and electrical signaling between two adjacent cells. Gap junction intercellular communication has been implicated in the regulation of various cellular processes, including cell migration, cell proliferation, cell differentiation, and cell apoptosis. This study aimed to determine the presence and functionality of gap junctions in human embryonic stem cells (hESCs). Using reverse transcription—polymerase chain reaction and immunocytochemistry, we demonstrate that human ES cells express two gap junction proteins, connexin 43 and connexin 45. Western blot analysis revealed the presence of three phosphorylated forms (nonphosphorylated [NP], P1, and P2) of connexin 43, NP being prominent. Moreover, scrape loading/dye transfer assay indicates that human ES cells are coupled through functional gap junctions that are inhibited by protein kinase C activation and extracellular signal-regulated kinase inhibition.




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