TY - JOUR
T1 - Cellular conservation of endangered midget buffalo (Lowland Anoa, Bubalus quarlesi) by establishment of primary cultured cell, and its immortalization with expression of cell cycle regulators
AU - Fukuda, Tomokazu
AU - Iino, Yuuka
AU - Eitsuka, Takahiro
AU - Onuma, Manabu
AU - Katayama, Masafumi
AU - Murata, Koichi
AU - Inoue-Murayama, Miho
AU - Hara, Kumiko
AU - Isogai, Emiko
AU - Kiyono, Tohru
N1 - Funding Information:
We thank Dr. Hiroyuki Miyoshi (RIKEN, BioResource Center) for providing lentiviral constructs. This work was supported by the research grant, JSPS KAKENHI.
Publisher Copyright:
© 2016, Springer Science+Business Media Dordrecht.
PY - 2016/10/1
Y1 - 2016/10/1
N2 - Lowland Anoa has become endangered due to hunting and human activity. Protection and breeding of endangered species in a controlled environment is the best way of conservation. However, it is not possible to adopt this approach for all endangered species because of the cost involved and the ever-increasing number of critically endangered species. In consideration of these limitations to the conventional conservation methods, we established a primary cell culture of endangered buffalo (Lowland Anoa, Bubalus quarlesi), for the preservation of this biological resource. In addition, we introduced human derived, mutant cyclin dependent kinase 4 (CDK4), Cyclin D, and telomerase reverse transcriptase (TERT) into the primary cells. The successful introduction of these three genes was confirmed by western blot with specific antibodies, and enzymatic activity. We also showed that the expression of mutant CDK4, Cyclin D, and TERT allows us to efficiently establish an immortalized cell line, with an intact chromosome pattern, from Lowland Anoa. To the best of our knowledge, this study is the first investigation that established an immortalized cell line of an endangered wild animal species.
AB - Lowland Anoa has become endangered due to hunting and human activity. Protection and breeding of endangered species in a controlled environment is the best way of conservation. However, it is not possible to adopt this approach for all endangered species because of the cost involved and the ever-increasing number of critically endangered species. In consideration of these limitations to the conventional conservation methods, we established a primary cell culture of endangered buffalo (Lowland Anoa, Bubalus quarlesi), for the preservation of this biological resource. In addition, we introduced human derived, mutant cyclin dependent kinase 4 (CDK4), Cyclin D, and telomerase reverse transcriptase (TERT) into the primary cells. The successful introduction of these three genes was confirmed by western blot with specific antibodies, and enzymatic activity. We also showed that the expression of mutant CDK4, Cyclin D, and TERT allows us to efficiently establish an immortalized cell line, with an intact chromosome pattern, from Lowland Anoa. To the best of our knowledge, this study is the first investigation that established an immortalized cell line of an endangered wild animal species.
KW - Cellular conservation
KW - Cultured cells
KW - Endangered animals
KW - Immortalization
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U2 - 10.1007/s10616-016-0004-0
DO - 10.1007/s10616-016-0004-0
M3 - Article
AN - SCOPUS:84979574370
VL - 68
SP - 1937
EP - 1947
JO - Cytotechnology
JF - Cytotechnology
SN - 0920-9069
IS - 5
ER -