The Role of Genetically Modified Human Feeder Cells in Maintaining the Integrity of Primary Cultured Human Deciduous Dental Pulp Cells.
The Role of Genetically Modified Human Feeder Cells in Maintaining the Integrity of Primary Cultured Human Deciduous Dental Pulp Cells.
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DOI:
10.3390/jcm11206087
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发表时间:
2022-10-15
影响因子:
3.9
通讯作者:
Saitoh I
中科院分区:
文献类型:
--
作者:
Ibano N;Inada E;Otake S;Kiyokawa Y;Sakata K;Sato M;Kubota N;Noguchi H;Iwase Y;Murakami T;Sawami T;Kakihara Y;Maeda T;Terunuma M;Terao Y;Saitoh I
Tissue-specific stem cells exist in tissues and organs, such as skin and bone marrow. However, their pluripotency is limited compared to embryonic stem cells. Culturing primary cells on plastic tissue culture dishes can result in the loss of multipotency, because of the inability of tissue-specific stem cells to survive in feeder-less dishes. Recent findings suggest that culturing primary cells in medium containing feeder cells, particularly genetically modified feeder cells expressing growth factors, may be beneficial for their survival and proliferation. Therefore, the aim of this study was to elucidate the role of genetically modified human feeder cells expressing growth factors in maintaining the integrity of primary cultured human deciduous dental pulp cells. Feeder cells expressing leukemia inhibitory factor, bone morphogenetic protein 4, and basic fibroblast growth factor were successfully engineered, as evidenced by PCR. Co-culturing with mitomycin-C-treated feeder cells enhanced the proliferation of newly isolated human deciduous dental pulp cells, promoted their differentiation into adipocytes and neurons, and maintained their stemness properties. Our findings suggest that genetically modified human feeder cells may be used to maintain the integrity of primary cultured human deciduous dental pulp cells.
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影响因子:
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作者:
Amit, M;Carpenter, MK;Thomson, JA
通讯作者:
Thomson, JA
影响因子:
5.6
作者:
Sato M;Maeda K;Koriyama M;Inada E;Saitoh I;Miura H;Ohtsuka M;Nakamura S;Sakurai T;Watanabe S;Miyoshi K
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Miyoshi K
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Kim GH;Lee GR;Choi HI;Park NH;Chung HT;Han IS
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Han IS
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Wang, Yaping
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通讯作者:
Hotta, T