Ghanavatinejad Fatemeh, Fard Tabrizi Zahra Pourteymour, Omidghaemi Shadi, Sharifi Esmaeel, Møller Simon Geir, Jami Mohammad-Saeid
Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Science, Shahrekord, Iran.
Department of Tissue Engineering and Biomaterials, School of Advanced Medical Sciences and Technologies, Hamadan University of Medical Sciences, Hamadan, Iran.
J Otol. 2019 Sep;14(3):77-88. doi: 10.1016/j.joto.2019.03.001. Epub 2019 Mar 23.
The utilization of biomarkers for and research is growing rapidly. This is mainly due to the enormous potential of biomarkers in evaluating molecular and cellular abnormalities in cell models and in tissue, and evaluating drug responses and the effectiveness of therapeutic intervention strategies. An important way to analyze the development of the human body is to assess molecular markers in embryonic specialized cells, which include the ectoderm, mesoderm, and endoderm. Neuronal development is controlled through the gene networks in the neural crest and neural tube, both components of the ectoderm. The neural crest differentiates into several different tissues including, but not limited to, the peripheral nervous system, enteric nervous system, melanocyte, and the dental pulp. The neural tube eventually converts to the central nervous system. This review provides an overview of the differentiation of the ectoderm to a fully functioning nervous system, focusing on molecular biomarkers that emerge at each stage of the cellular specialization from multipotent stem cells to completely differentiated cells. Particularly, the otic placode is the origin of most of the inner ear cell types such as neurons, sensory hair cells, and supporting cells. During the development, different auditory cell types can be distinguished by the expression of the neurogenin differentiation factor1 (Neuro D1), Brn3a, and transcription factor GATA3. However, the mature auditory neurons express other markers including βIII tubulin, the vesicular glutamate transporter (VGLUT1), the tyrosine receptor kinase B and C (Trk B, C), BDNF, neurotrophin 3 (NT3), Calretinin, etc.
生物标志物在[具体领域1]和[具体领域2]研究中的应用正在迅速增长。这主要是由于生物标志物在评估细胞模型和组织中的分子及细胞异常、评估药物反应以及治疗干预策略的有效性方面具有巨大潜力。分析人体发育的一个重要方法是评估胚胎特化细胞中的分子标志物,这些细胞包括外胚层、中胚层和内胚层。神经元发育是通过神经嵴和神经管中的基因网络控制的,这两者都是外胚层的组成部分。神经嵴分化为几种不同的组织,包括但不限于外周神经系统、肠神经系统、黑素细胞和牙髓。神经管最终转变为中枢神经系统。本综述概述了外胚层向功能完备的神经系统的分化过程,重点关注从多能干细胞到完全分化细胞的细胞特化每个阶段出现的分子生物标志物。特别地,耳基板是大多数内耳细胞类型(如神经元、感觉毛细胞和支持细胞)的起源。在发育过程中,不同的听觉细胞类型可以通过神经生成素分化因子1(Neuro D1)、Brn3a和转录因子GATA3的表达来区分。然而,成熟的听觉神经元表达其他标志物,包括βIII微管蛋白、囊泡谷氨酸转运体(VGLUT1)、酪氨酸受体激酶B和C(Trk B、C)、脑源性神经营养因子(BDNF)、神经营养因子3(NT3)、钙视网膜蛋白等。