Goorha Sarita, Reiter Lawrence T
Department of Neurology, University of Tennessee Health Science Center, Memphis, Tennessee.
Department of Pediatrics, University of Tennessee Health Science Center, Memphis, Tennessee.
Curr Protoc Hum Genet. 2017 Jan 11;92:21.6.1-21.6.10. doi: 10.1002/cphg.28.
A major issue in studying human neurogenetic disorders, especially rare syndromes affecting the nervous system, is the ability to grow neuronal cultures that accurately represent these disorders for analysis. Although there has been some success in generating induced pluripotent stem (iPS) cells from both skin and blood, there are still limitations to the collection and production of iPS cells from these biospecimens. We have had significant success in collecting and growing human dental pulp stem (DPS) cells from exfoliated teeth sent to our laboratory by the parents of children with a variety of rare neurogenetic syndromes. This protocol outlines our current methods for the growth and expansion of DPS cells from exfoliated (baby) teeth. These DPS cells can be differentiated into a variety of cell types including osteoblasts, chondrocytes, and mixed neuron and glial cultures. Here we provide our protocol for the differentiation of early passage DPS cell cultures into neurons for molecular studies. © 2017 by John Wiley & Sons, Inc.
研究人类神经遗传疾病,尤其是影响神经系统的罕见综合征时,一个主要问题是能否培养出能准确代表这些疾病以供分析的神经元培养物。尽管从皮肤和血液中生成诱导多能干细胞(iPS细胞)已取得了一些成功,但从这些生物样本中收集和生产iPS细胞仍存在局限性。我们从患有各种罕见神经遗传综合征儿童的父母送到我们实验室的脱落乳牙中成功收集并培养了人牙髓干细胞(DPS细胞)。本方案概述了我们目前从脱落(乳牙)牙齿中培养和扩增DPS细胞的方法。这些DPS细胞可分化为多种细胞类型,包括成骨细胞、软骨细胞以及混合的神经元和神经胶质细胞培养物。在此,我们提供将早期传代的DPS细胞培养物分化为神经元用于分子研究的方案。© 2017约翰威立父子出版公司