Pharmacological Retention of Oral Mucosa Progenitor/Stem Cells

被引:16
|
作者
Izumi, K. [1 ,5 ]
Inoki, K. [3 ,4 ]
Fujimori, Y. [2 ]
Marcelo, C. L. [2 ]
Feinberg, S. E. [1 ]
机构
[1] Univ Michigan, Dept Surg, Sect Oral & Maxillofacial Surg, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Surg, Plast & Reconstruct Surg Sect, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[5] Niigata Univ, Div Oral Anat, Grad Sch Med & Dent Sci, Niigata, Japan
关键词
oral keratinocyte; progenitor/stem cell; mTOR; rapamycin; EPIDERMAL STEM-CELLS; NECK-CANCER; MAMMALIAN TARGET; SURFACE MARKERS; KERATINOCYTE; RAPAMYCIN; MTOR; HEAD; SIZE; DIFFERENTIATION;
D O I
10.1177/0022034509350559
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Oral mucosa progenitor/stem cells reside as a small-sized cell population that eventually differentiates concurrently with an increase in cell size. Activation of the mammalian target of rapamycin (mTOR) leads to an increase in cell size. We hypothesized that rapamycin, a specific inhibitor of mTOR, will maintain primary human oral keratinocytes as a small-sized, undifferentiated cell population capable of retaining their proliferative capacity. Primary, rapamycin-treated (2 nM, 20 nM) oral keratinocytes showed a diminished cell size that correlated with a higher clonogenicity, a longer-term proliferative potential, and a slower cycling cell population concurrent with decreased expression of a differentiation marker when compared with untreated cells. Only the 2-nM rapamycin-treated oral keratinocytes maintained their ability to regenerate oral mucosa in vitro after 15 weeks of culture. Rapamycin, a Food and Drug Administration-approved drug, may have applicability for use in creating a highly proliferative cell population for use in regenerative medicine.
引用
收藏
页码:1113 / 1118
页数:6
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