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小分子筛选鉴定出可靶向的斑马鱼色素沉着途径。

Small molecule screening identifies targetable zebrafish pigmentation pathways.

机构信息

Developmental Biology Programme, Centre for Regenerative Medicine, Department of Biology and Biochemistry, University of Bath, Bath, UK.

出版信息

Pigment Cell Melanoma Res. 2012 Mar;25(2):131-43. doi: 10.1111/j.1755-148X.2012.00977.x.

Abstract

Small molecules complement genetic mutants and can be used to probe pigment cell biology by inhibiting specific proteins or pathways. Here, we present the results of a screen of active compounds for those that affect the processes of melanocyte and iridophore development in zebrafish and investigate the effects of a few of these compounds in further detail. We identified and confirmed 57 compounds that altered pigment cell patterning, number, survival, or differentiation. Additional tissue targets and toxicity of small molecules are also discussed. Given that the majority of cell types, including pigment cells, are conserved between zebrafish and other vertebrates, we present these chemicals as molecular tools to study developmental processes of pigment cells in living animals and emphasize the value of zebrafish as an in vivo system for testing the on- and off-target activities of clinically active drugs.

摘要

小分子可以补充遗传突变体,并可通过抑制特定蛋白质或途径来探究色素细胞生物学。在这里,我们展示了针对影响斑马鱼黑素细胞和虹彩细胞发育过程的活性化合物的筛选结果,并进一步详细研究了其中一些化合物的作用。我们鉴定并证实了 57 种可改变色素细胞形态发生、数量、存活或分化的化合物。还讨论了小分子的其他组织靶标和毒性。鉴于包括色素细胞在内的大多数细胞类型在斑马鱼和其他脊椎动物之间是保守的,我们将这些化学物质作为研究活体动物中色素细胞发育过程的分子工具,并强调了斑马鱼作为体内系统测试临床有效药物的靶标和脱靶活性的价值。

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