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Updated: Jun 2, 2026

Production of Genetically Engineered Golden Syrian Hamsters by Pronuclear Injection of the CRISPR/Cas9 Complex
Published on: January 9, 2018
On the use of Syrian-hamster cell-cultures as targets for carcinogen-screening
1WAYNE STATE UNIV,CHILDRENS HOSP MICHIGAN,SCH MED,DEPT PEDIAT,CELL CULTURE LAB,DETROIT,MI 48201.
Abstract:
Syrian hamster embryo (SHE) cells have a reported culture lifespan limited to 30 to 40 population doublings (PDs). In contrast, we have observed continuous growth of two SHE cell lines without the hallmarks of cellular senescence. Two independent primary isolates (SHE-3, and SHE-15) have been grown for more than 160 PDs (SHE-3) and 50 PDs (SHE-15), respectively, with weekly subcultures and with no sign of senescence. During this study, we observed that SHE-3 cells ceased to multiply after about 30 PDs when grown in a nutritionally-inadequate serum-free medium, but resumed growth when switched to an adequate medium. The chromosomal profiles of both SHE cultures revealed a near diploid karyotype but not a completely normal karyotype, even at early passages with increasing chromosomal changes with continued culture. In addition, Syrian hamster chondrocytes were isolated, partially characterized, and their sensitivity to chemically-induced morphological transformation was compared to that of the standard Syrian hamster embryo (SHE) mixed cell culture. It appears that chondrocytes may be a suitable and more sensitive target for carcinogen-screening in vitro.
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