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Anaplastic Lymphoma Kinase Is Required for Neurogenesis in the Developing Central Nervous System of Zebrafish

机译:发育不良的淋巴瘤激酶是斑马鱼中枢神经系统发育中神经发生所必需的。

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摘要

Anaplastic Lymphoma Kinase (ALK) was initially discovered as an oncogene in human lymphoma and other cancers, including neuroblastoma. However, little is known about the physiological function of ALK. We identified the alk ortholog in zebrafish (Danio rerio) and found that it is highly expressed in the developing central nervous system (CNS). Heat-shock inducible transgenic zebrafish lines were generated to over-express alk during early neurogenesis. Its ectopic expression resulted in activation of the MEK/ERK pathway, increased cell proliferation, and aberrant neurogenesis leading to mis-positioning of differentiated neurons. Thus, overexpressed alk is capable of promoting cell proliferation in the nervous system, similar to the situation in ALK-related cancers. Next, we used Morpholino mediated gene knock-down and a pharmacological inhibitor to interfere with expression and function of endogenous Alk. Alk inhibition did not affect neuron progenitor formation but severely compromised neuronal differentiation and neuron survival in the CNS. These data indicate that tightly controlled alk expression is critical for the balance between neural progenitor proliferation, differentiation and survival during embryonic neurogenesis.
机译:间变性淋巴瘤激酶(ALK)最初被发现是人类淋巴瘤和其他癌症(包括神经母细胞瘤)的癌基因。然而,关于ALK的生理功能知之甚少。我们鉴定了斑马鱼中的直向同源物(Danio rerio),发现它在发育中的中枢神经系统(CNS)中高度表达。产生热休克诱导的转基因斑马鱼品系,以在早期神经发生过程中过表达烷烃。它的异位表达导致MEK / ERK通路的激活,细胞增殖的增加和神经发生异常,从而导致分化神经元的位置错误。因此,与ALK相关的癌症类似,过表达的alk能够促进神经系统中的细胞增殖。接下来,我们使用Morpholino介导的基因敲低和药理抑制剂来干扰内源性Alk的表达和功能。抑制ALK不会影响神经元祖细胞的形成,但会严重损害CNS中神经元的分化和神经元的存活。这些数据表明,严格控制的alk表达对于胚胎神经发生过程中神经祖细胞增殖,分化和存活之间的平衡至关重要。

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