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神经生物学中使用 SH-SY5Y 神经母细胞瘤细胞的注意事项。

Considerations for the Use of SH-SY5Y Neuroblastoma Cells in Neurobiology.

机构信息

Department of Neuroscience, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.

Molecular Studies of Neurodegenerative Diseases Lab, FELS Institute, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.

出版信息

Methods Mol Biol. 2021;2311:9-23. doi: 10.1007/978-1-0716-1437-2_2.

Abstract

The use of primary mammalian neurons derived from embryonic central nervous system tissue is limited by the fact that once terminally differentiated into mature neurons, the cells can no longer be propagated. Transformed neuronal-like cell lines can be used in vitro to overcome this limitation. However, several caveats exist when utilizing cells derived from malignant tumors. In this context, the popular SH-SY5Y neuroblastoma cell line and its use in in vitro systems is described. Originally derived from a metastatic bone tumor biopsy, SH-SY5Y (ATCC CRL-2266™) cells are a subline of the parental line SK-N-SH (ATCC HTB-11™). SK-N-SH were subcloned three times; first to SH-SY, then to SH-SY5, and finally to SH-SY5Y. SH-SY5Y were deposited to the ATCC in 1970 by June L. Biedler. Three important characteristics of SH-SY5Y cells should be considered when using these cells in in vitro studies. First, cultures include both adherent and floating cells, both types of which are viable. Few studies address the biological significance of the adherent versus floating phenotypes, but most reported studies utilize adherent populations and discard the floating cells during media changes. Second, early studies by Biedler's group indicated that the parental differentiated SK-N-SH cells contained two morphologically distinct phenotypes: neuroblast-like cells and epithelial-like cells (Ross et al., J Natl Cancer Inst 71(4):741-747, 1983). These two phenotypes may correspond to the "N" and "S" types described in later studies in SH-SY5Y by Encinas et al. (J Neurochem 75(3):991-1003, 2000). Cells with neuroblast-like morphology are positive for tyrosine hydroxylase (TH) and dopamine-β-hydroxylase characteristic of catecholaminergic neurons, whereas the epithelial-like counterpart cells lacked these enzymatic activities (Ross et al., J Natl Cancer Inst 71(4):741-747, 1983). Third, SH-SY5Y cells can be differentiated to a more mature neuron-like phenotype that is characterized by neuronal markers. There are several methods to differentiate SH-SY5Y cells and are mentioned below. Retinoic acid is the most commonly used means for differentiation and will be addressed in detail.

摘要

从胚胎中枢神经系统组织中获得的原代哺乳动物神经元的使用受到以下事实的限制

一旦终末分化为成熟神经元,细胞就不能再增殖。转化的类神经元细胞系可用于体外克服这一限制。然而,当利用源自恶性肿瘤的细胞时,存在几个注意事项。在这种情况下,描述了流行的 SH-SY5Y 神经母细胞瘤细胞系及其在体外系统中的用途。SH-SY5Y(ATCC CRL-2266™)细胞最初源自转移性骨肿瘤活检,源自亲本系 SK-N-SH(ATCC HTB-11™)的亚系。SK-N-SH 被克隆了三次;第一次是 SH-SY,然后是 SH-SY5,最后是 SH-SY5Y。1970 年,June L. Biedler 将 SH-SY5Y 细胞存入 ATCC。在体外研究中使用这些细胞时,应考虑 SH-SY5Y 细胞的三个重要特征。首先,培养物包括贴壁细胞和悬浮细胞,这两种细胞都是有活力的。很少有研究涉及贴壁表型与悬浮表型的生物学意义,但大多数报道的研究都利用贴壁群体,并在更换培养基时丢弃悬浮细胞。其次,Biedler 小组的早期研究表明,亲本分化的 SK-N-SH 细胞含有两种形态上明显不同的表型:神经母细胞瘤样细胞和上皮样细胞(Ross 等人,J Natl Cancer Inst 71(4):741-747, 1983)。这两种表型可能对应于后来 Encinas 等人在 SH-SY5Y 中描述的“N”和“S”类型(J Neurochem 75(3):991-1003, 2000)。具有神经母细胞瘤样形态的细胞对酪氨酸羟化酶(TH)和多巴胺-β-羟化酶呈阳性,这些酶是儿茶酚胺能神经元的特征,而相应的上皮样细胞则缺乏这些酶活性(Ross 等人,J Natl Cancer Inst 71(4):741-747, 1983)。第三,SH-SY5Y 细胞可以分化为更成熟的神经元样表型,其特征是神经元标志物。有几种方法可以分化 SH-SY5Y 细胞,下面将提到这些方法。视黄酸是最常用的分化手段,将详细讨论。

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