ZIP14 Deletion Disrupts Divalent Metal Homeostasis in Mouse Cerebrospinal Fluid

IF 2.7 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shannon M. McCabe, Ningning Zhao
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引用次数: 0

Abstract

ZIP14 is a member of the SLC39A (ZIP) family of metal transporters, primarily facilitating the cellular influx of divalent metals including manganese (Mn), zinc (Zn), and iron (Fe). Previous studies have demonstrated that Zip14 knockout (Zip14-/-) mice exhibit significant increases in whole blood and brain Mn levels. However, the impact of ZIP14 deletion on metal homeostasis within the cerebrospinal fluid (CSF) remained unexplored. In this study, we comprehensively assessed Mn, Zn, Fe, sodium (Na), potassium (K), and calcium (Ca) levels in whole blood, serum, and CSF of male and female Zip14-/- mice to elucidate both systemic and central nervous system (CNS)-specific alterations in metal homeostasis. Our findings reveal that Zip14-/- mice exhibit pronounced Mn accumulation, with CSF Mn levels increasing by approximately 15-fold in males and 46-fold in females compared to wild-type controls. Correspondingly, blood Mn levels rose 23-fold in males and 17-fold in females, while serum Mn levels increased 10-fold and 15-fold, respectively. In contrast, Zn and Fe levels in whole blood and serum remained comparable between Zip14-/- and wild-type mice. However, significant elevations in CSF Zn were observed, with a sevenfold increase in males and a 16-fold increase in females, alongside a threefold rise in CSF Fe levels in females. The CSF to serum ratios of Zn and Fe remained below 1 but were increased in the knockout mice, suggesting the activation of alternative metal transporters in the absence of ZIP14, which may contribute to the increased Mn accumulation in the CSF as well. Importantly, Na⁺ and K⁺ levels in whole blood, serum, and CSF were unaltered in Zip14-/- mice, indicating that ZIP14 deletion does not broadly disrupt systemic electrolyte balance or compromise blood—CSF barrier integrity. Conversely, CSF Ca²⁺ levels were significantly reduced by 33% in male and 23% in female Zip14-/- mice, suggesting a specific effect of ZIP14 on calcium homeostasis within the CNS.

ZIP14缺失破坏小鼠脑脊液二价金属稳态
ZIP14是SLC39A (ZIP)金属转运蛋白家族的成员,主要促进包括锰(Mn)、锌(Zn)和铁(Fe)在内的二价金属的细胞内流。先前的研究表明,Zip14敲除(Zip14-/-)小鼠的全血和脑锰水平显著升高。然而,ZIP14缺失对脑脊液(CSF)内金属稳态的影响尚不清楚。在这项研究中,我们综合评估了雄性和雌性Zip14-/-小鼠全血、血清和脑脊液中Mn、Zn、Fe、钠(Na)、钾(K)和钙(Ca)的水平,以阐明全身和中枢神经系统(CNS)特异性金属稳态的改变。我们的研究结果显示,Zip14-/-小鼠表现出明显的Mn积累,与野生型对照相比,雄性CSF Mn水平增加了约15倍,雌性增加了46倍。相应的,男性血锰水平上升了23倍,女性上升了17倍,而血清锰水平分别上升了10倍和15倍。相比之下,Zip14-/-和野生型小鼠的全血和血清中锌和铁水平保持相当。然而,观察到脑脊液锌显著升高,男性增加7倍,女性增加16倍,女性脑脊液铁水平增加3倍。敲除小鼠脑脊液中Zn和Fe与血清的比值保持在1以下,但在敲除小鼠中升高,提示在ZIP14缺失的情况下,替代金属转运体被激活,这可能也导致了脑脊液中Mn积累的增加。重要的是,在Zip14-/-小鼠中,Na +和K +在全血、血清和脑脊液中的水平没有改变,表明Zip14缺失不会广泛破坏全身电解质平衡或损害血-脑脊液屏障的完整性。相反,CSF Ca 2 +在雄性和雌性Zip14-/-小鼠中显著降低33%和23%,表明Zip14对CNS内钙稳态有特异性影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Biochemistry and Function
Cell Biochemistry and Function 生物-生化与分子生物学
CiteScore
6.20
自引率
0.00%
发文量
93
审稿时长
6-12 weeks
期刊介绍: Cell Biochemistry and Function publishes original research articles and reviews on the mechanisms whereby molecular and biochemical processes control cellular activity with a particular emphasis on the integration of molecular and cell biology, biochemistry and physiology in the regulation of tissue function in health and disease. The primary remit of the journal is on mammalian biology both in vivo and in vitro but studies of cells in situ are especially encouraged. Observational and pathological studies will be considered providing they include a rational discussion of the possible molecular and biochemical mechanisms behind them and the immediate impact of these observations to our understanding of mammalian biology.
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