Hedgehog signalling is dispensable in the proliferation of stem cells from human exfoliated deciduous teeth

被引:3
作者
Ejeian, Fatemeh [1 ]
Baharvand, Hossein [2 ,3 ]
Nasr-Esfahani, Mohammad Hossein [1 ]
机构
[1] ACECR, Cell Sci Res Ctr, Royan Inst Biotechnol, Dept Cellular Biotechnol, Esfahan, Iran
[2] ACECR, Cell Sci Res Ctr, Royan Inst Stem Cell Biol & Technol, Dept Stem Cells & Dev Biol, Tehran, Iran
[3] Univ Sci & Culture, ACECR, Dept Dev Biol, Tehran, Iran
关键词
neural progenitor; sonic hedgehog; SHED; proliferation; VERTEBRATE NEURAL-TUBE; SONIC-HEDGEHOG; IN-VITRO; TISSUE-REPAIR; CREST CELLS; DIFFERENTIATION; MECHANISM; CYCLE; PROGENITORS; CEREBELLUM;
D O I
10.1002/cbin.10227
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The hedgehog (Hh) signalling pathway is one of the key regulators in development with a dual role in cell fate specification, proliferation, and survival on different target cells. We have investigated the effect of recombinant sonic hedgehog (r-SHH) on extracted multipotent stem cells from human exfoliated deciduous teeth (SHED), which represent a potential stem cell population for therapeutic applications. Cell proliferation and cycle assays shown that r-SHH did not have a distinctive effect on cell cycle progression, nor did it increase cell number over a wide range of concentrations. Quantitative polymerase chain reaction (Q-PCR) also suggests that r-SHH treatment has no demonstrable influence on expression of proliferative genes (CCNE1 and KI67); in contrast, the anti-proliferative gene (CDKN1A) is overexpressed in response to SHH. Our findings have suggested the possibility that SHEDs demonstrate a different potential from human bone marrow mesenchymal stem cells (h-BMSCs) and dorsal neural progenitor in response to growth factors such as SHH.
引用
收藏
页码:480 / 487
页数:8
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