RRC ID 10812
Author Shitara S, Kakeda M, Nagata K, Hiratsuka M, Sano A, Osawa K, Okazaki A, Katoh M, Kazuki Y, Oshimura M, Tomizuka K.
Title Telomerase-mediated life-span extension of human primary fibroblasts by human artificial chromosome (HAC) vector.
Journal Biochem Biophys Res Commun
Abstract Telomerase-mediated life-span extension enables the expansion of normal cells without malignant transformation, and thus has been thought to be useful in cell therapies. Currently, integrating vectors including the retrovirus are used for human telomerase reverse transcriptase (hTERT)-mediated expansion of normal cells; however, the use of these vectors potentially causes unexpected insertional mutagenesis and/or activation of oncogenes. Here, we established normal human fibroblast (hPF) clones retaining non-integrating human artificial chromosome (HAC) vectors harboring the hTERT expression cassette. In hTERT-HAC/hPF clones, we observed the telomerase activity and the suppression of senescent-associated SA-beta-galactosidase activity. Furthermore, the hTERT-HAC/hPF clones continued growing beyond 120days after cloning, whereas the hPF clones retaining the silent hTERT-HAC senesced within 70days. Thus, hTERT-HAC-mediated episomal expression of hTERT allows the extension of the life-span of human primary cells, implying that gene delivery by non-integrating HAC vectors can be used to control cellular proliferative capacity of primary cultured cells.
Volume 369(3)
Pages 807-11
Published 2008-5-9
DOI 10.1016/j.bbrc.2008.02.119
PII S0006-291X(08)00287-8
PMID 18328257
MeSH Animals CHO Cells Cell Division Cell Proliferation* Cellular Senescence Chromosomes, Artificial, Human / genetics* Cricetinae Cricetulus Fibroblasts / enzymology Fibroblasts / physiology Gene Transfer Techniques Genetic Vectors / genetics* Humans Telomerase / analysis Telomerase / genetics*
IF 2.985
Times Cited 15
WOS Category BIOPHYSICS BIOCHEMISTRY & MOLECULAR BIOLOGY
Resource
Human and Animal Cells HFL-I(RCB0521)