Establishment of segmental identity in embryonic stem cell derived motor neurons

描述（由申请人提供）：运动功能取决于发育中的神经管内数百种不同运动神经元（MN）亚型的规格。运动神经元亚型的身份是由前后（AP）模式信号，细分成分子和功能不同的片段，否则均匀的神经管。在比较详细的了解背腹图案和规范的通用MN身份，相对较少的是知道的分子机制的脊髓前后图案和收购MN亚型身份。在这里，我们利用我们的能力，直接分化的ES细胞到运动神经元获得不同的亚型身份在体外。我们将使用这个系统来研究获得前后身份的遗传级联：1）我们将定义调节AP模式的外在信号; 2）我们将定义AP身份巩固的时间点; 3）我们将定义这一过程的分子程序。深入了解在ES细胞分化过程中获得特定神经元节段和亚型身份的过程将对利用ES细胞研究和治疗神经退行性疾病产生影响。个体运动神经元亚型对变性的不同易感性可能揭示治疗干预的新的潜在靶点。此外，我们指导MN亚型鉴定的能力对于有效实施MN细胞替代疗法至关重要。

DESCRIPTION (provided by applicant): Motor function depends on specification of hundreds of distinct motor neuron (MN) subtypes within the developing neural tube. The motor neuron subtype identity is determined by anteroposterior (AP) patterning signals that subdivide the otherwise uniform neural tube into molecularly and functionally distinct segments. In comparison to the detailed understanding of dorsoventral patterning and specification of the generic MN identity, relatively little is known about the molecular mechanisms underlying anteroposterior patterning of the spinal cord and acquisition of MN subtype identity. Here we take advantage of our ability to direct differentiation of ES cells into motor neurons acquiring distinct subtype identities in vitro. We will use this system to study the genetic cascade underlying the acquisition of anteroposterior identity: 1) we will define extrinsic signals that regulate AP patterning; 2) we will define the time point during which AP identity is consolidated and 3) we will define molecular programs that underlie this process. Gaining insight into the process of acquisition of specific neuronal segmental and subtype identities during ES cell differentiation will have an impact on the utilization of ES cells to study and treat neurodegenerative diseases. The differential susceptibility of individual motor neuron subtypes to degeneration might reveal new potential targets for therapeutic intervention. In addition, our ability to direct MN subtype identity will be essential for effective implementation of MN cell replacement therapies.