Stem cells from human-exfoliated deciduous teeth can regenerate central nervous system
Stem cells from human-exfoliated deciduous teeth can regenerate central nervous system
批准号:
22390372
负责人:
YAMAMOTO Akihito
金额:
$12.9万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2010
资助国家:
日本
项目状态:
已结题
起止时间:
2010 至 2012
中文摘要
我们研究了成人智齿(DPSC)和脱落乳牙(SHED)牙髓干细胞的多分化能力、表型标记表达和转录组谱。数据显示,表达多种神经谱系标志物的SHED和DPSC均能分化神经元、星形胶质细胞、少突胶质细胞、成骨细胞、脂肪细胞和软骨细胞。此外,我们优化了方案,使SHED和DPSC特异性分化为表达多巴胺能神经元的酪氨酸羟化酶。在临床前分析中,我们发现SHED和DPSC治疗脊髓损伤、缺氧脑损伤和帕金森病的疗效显著。除了其显著的神经再生活性外,我们没有观察到移植的细胞在植入8周后的恶性转化。从脱落的乳牙和阻生的成人智齿中可以获得细胞和DPSCs,而不会对健康产生不良影响。因此,关于它们的临床应用很少有伦理问题。我们认为牙源性干细胞可能是治疗各种中枢神经系统疾病的一种极好的实用细胞资源。
英文摘要
We have characterized the multi-differentiation potency, phenotypic marker expression and trascriptome profile of dentalpulp derived stem cell from adult wisdom teeth (DPSC) and exfoliated deciduous teeth (SHED). The data showed that both SHED and DPSC expressing multiple neural linage markers are able to differentiate neuron, astrocyte, oligodendrocyte, osteoblast, adipocyte and chondrocytes. Furthermore, we have optimized the protocol allowing a specific differentiation of SHED and DPSC to tyrosine hydroxylase expressing dopaminerigic neurons. In pre-clinical analysis, we have found remarkable therapeutic benefits of SHED and DPSC for treatment of spinal cord injury, hypoxic brain injury and Parkinson’s disease. In addition to their remarkable neuro-regenerative activities, we did not observe the malignant transformation of engrafted SHEDs 8 weeks after theirimplantation. SHEDs and DPSCs can be obtained from exfoliated deciduous and impacted adult wisdom teeth without adverse health effects. Thus, there are few ethical concerns regarding their clinical use. We propose that tooth-derived stem cells may be an excellent and practical cellular resource for the treatment of various CNS diseases.
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Engrafted Dental Pulp Stem Cells Promoted Functional Recovery of Completely Transected Rat Spinal Cord
移植牙髓干细胞促进完全横断的大鼠脊髓功能恢复
DOI:
--
发表时间:
2011
期刊:
影响因子:
--
作者:
[Yoshida K, Sumita Y, Marukawa E, Harashima M, Asahina I, 三宅克也, 酒井清 山本朗仁 松原弘記 上田実]
通讯作者:
酒井清 山本朗仁 松原弘記 上田実
歯髄幹細胞を用いた脊髄損傷の再生医療
利用牙髓干细胞治疗脊髓损伤的再生医学
DOI:
--
发表时间:
2012
期刊:
Clinical Neuroscience
影响因子:
--
作者:
[Kiyoshi Sakai, Akihito Yamamoto#, Kohki Matsubara, Shoko Nakamura, Mami Naruse (#correspondence), Chie Matsuda, 山本朗仁]
通讯作者:
山本朗仁
DOI:
10.1172/jci59251
发表时间:
2012-01-01
期刊:
JOURNAL OF CLINICAL INVESTIGATION
影响因子:
15.9
作者:
[Sakai, Kiyoshi, Yamamoto, Akihito, Ueda, Minoru]
通讯作者:
Ueda, Minoru
歯髄幹細胞の培養上清を用いた中枢神経疾患治療用組成物
利用牙髓干细胞培养上清液治疗中枢神经系统疾病的组合物
DOI:
--
发表时间:
2010
期刊:
影响因子:
--
作者:
[]
通讯作者:
ドーパミン作動生ニューロンへ分化させたヒト歯髄幹細胞のパーキンソンモデルへの移植治療効果の検討
分化为多巴胺能活神经元的人牙髓干细胞移植入帕金森病模型的疗效观察
DOI:
--
发表时间:
2013
期刊:
影响因子:
--
作者:
[I T, Sumita Y, Minamizato T, Umebayashi M, Tran SD, Asahina I, 山本朗仁, 三宅克也,江上洋平,川合克久,荒木伸一, 藤井裕美 山本朗仁 伊藤美佳子 大野欽司 上田実]
通讯作者:
藤井裕美 山本朗仁 伊藤美佳子 大野欽司 上田実
共 19 条
Development of a novel treatment method for xerostomia by dental pulp stem cell-derived humoral factor
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批准号:17H04404
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$10.73万
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财政年份:2017
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负责人:YAMAMOTO Akihito
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依托单位:
Evaluation of the therapeutic benefits of anti-inflammatory M2 macrophage inducer for distraction osteogenesis
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批准号:15K15736
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项目类别:Grant-in-Aid for Challenging Exploratory Research
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资助金额:$2.33万
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财政年份:2015
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负责人:YAMAMOTO Akihito
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依托单位:
Development of regenerative therapy against severe peripheral nerve injury with a novel anti-inflammatory M2 macrophages inducer derived from dental pulp stem cells
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批准号:26293427
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$10.4万
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财政年份:2014
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负责人:YAMAMOTO Akihito
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Analysis of molecular forces for stem/progenitor cell homing in bone regeneration
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批准号:23659915
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项目类别:Grant-in-Aid for Challenging Exploratory Research
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资助金额:$2.33万
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财政年份:2011
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负责人:YAMAMOTO Akihito
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依托单位:
Roles of signaling regulation in the endoplasmic reticulum on the development of central nervous system
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批准号:17370074
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$10.29万
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财政年份:2005
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负责人:YAMAMOTO Akihito
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依托单位:
海外基金