激活素和骨形态发生蛋白存在于围产期感觉神经元靶组织中,可诱导神经肽。

A. K. Hall, R. Burke, Malini Anand, K. Dinsio
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引用次数: 30

摘要

先前的研究表明,感觉靶组织在naïve感觉神经元中诱导神经肽,激活素和骨形态发生蛋白(BMPs)能够在体外诱导胚胎感觉神经元中与伤害感觉相关的神经肽。本研究的目的是了解这些配体是否在正确的发育时期在天然感觉神经元靶组织中可用,以在体内发挥这种诱导作用。在胚胎发育后期,感觉神经元最初接触其周围目标组织并开始表达神经肽,我们证明激活素和bmp存在于胚胎和新生儿中,以调节感觉神经元的分化。利用配体特异性抗体对原生胚胎和新生儿靶组织进行免疫印迹和免疫组织化学研究。虽然活化素很容易溶解,但只有在高盐萃取后才能检测到bmp,这表明bmp与细胞外部分结合,只能在本地组织中局部起作用。一种抑制剂noggin在胚胎皮肤和肌肉中都存在。综上所述,这些数据表明神经元分化不太可能由配体的简单表达来调节,但配体的功能可用性是赋予生物活性的关键成分。
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Activin and bone morphogenetic proteins are present in perinatal sensory neuron target tissues that induce neuropeptides.
Previous studies have shown that sensory target tissues induce neuropeptides in naïve sensory neurons, and that activin and bone morphogenetic proteins (BMPs) are capable of inducing neuropeptides associated with nociception in embryonic sensory neurons in vitro. The goal of the present study was to learn if these ligands were available in native sensory neuron target tissues at correct developmental periods to play this inductive role in vivo. Sensory neurons initially contact their peripheral target tissues and begin to express neuropeptides during late embryogenesis, and we demonstrate that activin and BMPs are present in the embryo and neonate to regulate sensory neuron differentiation. Native embryonic and neonatal target tissues were analyzed by immunoblot and immunohistochemical studies using ligand-specific antibodies. Although activin was easily solubilized, BMPs were detected only after high salt extraction, suggesting that BMPs were bound to extracellular moieties and were capable of acting only locally in native tissues. One inhibitor, noggin, was present in both embryonic skin and muscle. In combination, these data suggest that neuronal differentiation is unlikely to be regulated by simple expression of ligand, but that the functional availability of ligand is a critical component confering biological activity.
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