Frederickson Christopher
NeuroBioTex, Inc., 101 Christopher Columbus Boulevard, Galveston, TX 77550, USA.
Sci STKE. 2003 May 13;2003(182):pe18. doi: 10.1126/stke.2003.182.pe18.
As recently as 20 years ago, all zinc in biological systems was believed to be tightly bound to proteins, and the idea of imaging zinc was considered heretical. Beginning with Maske's research with dithizonate staining of the hippocampus in the 1950s, however, zinc-sensitive dyes have indicated that, in mammalian cells, free zinc can exist in at least three separate pools. These pools include vesicular zinc sequestered in presynaptic vesicles and secretory granules, zinc released from these vesicles into the extracellular space after physiological stimulation, and transient increases in zinc in cells in the regions where extracellular release of zinc has occurred. This Perspective covers the zinc-imaging tools, from dithizonate to the newest FRET-based sensors, that have galvanized biomedical science.
就在20年前,生物系统中的所有锌都被认为与蛋白质紧密结合,而对锌进行成像的想法被视为异端邪说。然而,从20世纪50年代马斯克对海马体进行双硫腙染色的研究开始,锌敏感染料表明,在哺乳动物细胞中,游离锌至少可以存在于三个不同的池中。这些池包括储存在突触前囊泡和分泌颗粒中的囊泡锌、生理刺激后从这些囊泡释放到细胞外空间的锌,以及在锌发生细胞外释放的区域中细胞内锌的短暂增加。这篇综述涵盖了从双硫腙到最新的基于荧光共振能量转移(FRET)的传感器等锌成像工具,这些工具推动了生物医学科学的发展。