A Novel Method to Isolate Primordial Germ Cells and Its Use for the Generation of Germline Chimeras in Chicken

• Published in: Biology of reproduction 2007-07, Vol.77 (1), p.115-119
• Main Authors: YAMAMOTO, Yasuhiro, USUI, Fumitake, NAKAMURA, Yoshiaki, ITO, Yohei, TAGAMI, Takahiro, NIRASAWA, Keijiro, MATSUBARA, Yuko, ONO, Tamao, KAGAMI, Hiroshi
• Format: Article
• Language: English
• Subjects: Animals; Animals, Genetically Modified; Biological and medical sciences; Cell cultures. Hybridization. Fusion; Cell Separation - methods; Cells, Cultured; Chick Embryo; Chickens - genetics; Chimera - embryology; Chimera - genetics; Fundamental and applied biological sciences. Psychology; General aspects; Germ Cells - cytology; Germ Cells - metabolism; Molecular and cellular biology
• ISSN: 0006-3363; 1529-7268
• DOI: 10.1095/biolreprod.107.061200

A novel method was developed to isolate chick primordial germ cells (PGCs) from circulating embryonic blood. This is a very simple and rapid method for the isolation of circulating PGCs (cPGCs) using an ammonium chloride-potassium (ACK) buffer for lysis of the red blood cells. The PGCs were purified as in vitro culture proceeded. Most of the initial red blood cells were removed in the first step using the ACK lysis buffer. The purity of the cPGCs after ACK treatment was 57.1%, and the recovery rate of cPGCs from whole blood was 90.3%. The ACK process removed only red blood cells and it did not affect cPGC morphology. In the second step, the red blood cells disappeared as the culture progressed. At 7 days of in vitro culture, the purity of the PGCs was 92.9%. Most of these cells expressed germline-specific antibodies, such as those against chicken vasa homolog (CVH). The cultured PGCs expressed the Cvh and Dazl genes. Chimeric chickens were produced from these cultured PGCs, and the donor cells were detected in the gonads, suggesting that the PGCs had biological function. In conclusion, this novel isolation system for PGCs should be easier to use than previous methods. The results of the present study suggest that this novel method will become a powerful tool for germline manipulation in the chicken.