Immortalized Mouse Floxed Fam20c Dental Papillar Mesenchymal and Osteoblast Cell Lines Retain Their Primary Characteristics. Issue 11 (November 2015)
- Record Type:
- Journal Article
- Title:
- Immortalized Mouse Floxed Fam20c Dental Papillar Mesenchymal and Osteoblast Cell Lines Retain Their Primary Characteristics. Issue 11 (November 2015)
- Main Title:
- Immortalized Mouse Floxed Fam20c Dental Papillar Mesenchymal and Osteoblast Cell Lines Retain Their Primary Characteristics
- Authors:
- Liu, Chao
Wang, Xiaofang
Zhang, Hua
Xie, Xiaohua
Liu, Peihong
Liu, Ying
Jani, Priyam H.
Lu, Yongbo
Chen, Shuo
Qin, Chunlin - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="jcp25008-sec-0001" sec-type="section"> <p> <italic>Fam20c</italic> is essential for the normal mineralization of dentin and bone. The generation of odontoblast and osteoblast cell lines carrying floxed <italic>Fam20c</italic> allele can offer valuable tools for the study of the roles of <italic>Fam20c</italic> in the mineralization of dentin and bone. The limited capability of the primary odontoblasts and osteoblasts to proliferate necessitates the development of odontoblast and osteoblast cell lines serving as substitutes for the study of differentiation and mineralization of the odontoblasts and osteoblasts. In this study, we established and characterized immortalized mouse floxed <italic>Fam20c</italic> dental papilla mesenchymal and osteoblast cell lines. The isolated primary mouse floxed <italic>Fam20c</italic> dental papilla mesenchymal cells and osteoblasts were immortalized by the infection of lentivirus containing Simian Virus 40 T‐antigen (SV40 T‐Ag). The immortalization of floxed <italic>Fam20c</italic> dental papilla mesenchymal cells and osteoblasts was verified by the long‐term passages and genomic integration of SV40 T‐Ag. The immortalized floxed <italic>Fam20c</italic> dental papilla mesenchymal and osteoblast cell lines not only proliferated at a high rate and retained the morphology of their primary counterparts, but also preserved the dentin and<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="jcp25008-sec-0001" sec-type="section"> <p> <italic>Fam20c</italic> is essential for the normal mineralization of dentin and bone. The generation of odontoblast and osteoblast cell lines carrying floxed <italic>Fam20c</italic> allele can offer valuable tools for the study of the roles of <italic>Fam20c</italic> in the mineralization of dentin and bone. The limited capability of the primary odontoblasts and osteoblasts to proliferate necessitates the development of odontoblast and osteoblast cell lines serving as substitutes for the study of differentiation and mineralization of the odontoblasts and osteoblasts. In this study, we established and characterized immortalized mouse floxed <italic>Fam20c</italic> dental papilla mesenchymal and osteoblast cell lines. The isolated primary mouse floxed <italic>Fam20c</italic> dental papilla mesenchymal cells and osteoblasts were immortalized by the infection of lentivirus containing Simian Virus 40 T‐antigen (SV40 T‐Ag). The immortalization of floxed <italic>Fam20c</italic> dental papilla mesenchymal cells and osteoblasts was verified by the long‐term passages and genomic integration of SV40 T‐Ag. The immortalized floxed <italic>Fam20c</italic> dental papilla mesenchymal and osteoblast cell lines not only proliferated at a high rate and retained the morphology of their primary counterparts, but also preserved the dentin and bone specific gene expression as the primary dental papilla mesenchymal cells and osteoblasts did. Consistently, the capability of the primary floxed <italic>Fam20c</italic> dental papilla mesenchymal cells and osteoblasts to mineralize was also inherited by the immortalized dental papilla mesenchymal and osteoblast cell lines. Thus, we have successfully generated the immortalized mouse floxed <italic>Fam20c</italic> dental papilla mesenchymal and osteoblast cell lines. J. Cell. Physiol. 9999: 2581–2587, 2015. © 2015 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of cellular physiology. Volume 230:Issue 11(2015:Nov.)
- Journal:
- Journal of cellular physiology
- Issue:
- Volume 230:Issue 11(2015:Nov.)
- Issue Display:
- Volume 230, Issue 11 (2015)
- Year:
- 2015
- Volume:
- 230
- Issue:
- 11
- Issue Sort Value:
- 2015-0230-0011-0000
- Page Start:
- 2581
- Page End:
- 2587
- Publication Date:
- 2015-11
- Subjects:
- Physiology -- Periodicals
Cell physiology -- Periodicals
571.6 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4652 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcp.25008 ↗
- Languages:
- English
- ISSNs:
- 0021-9541
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.020000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3520.xml