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高锌血症和高钙卫蛋白血症:一种锌代谢的新紊乱疾病。

Hyperzincaemia and hypercalprotectinaemia: a new disorder of zinc metabolism.

作者信息

Sampson Barry, Fagerhol Magne K, Sunderkötter Cord, Golden Barbara E, Richmond Peter, Klein Nigel, Kovar Ilya Z, Beattie John H, Wolska-Kusnierz Beata, Saito Yoshiaki, Roth Johannes

机构信息

Department of Clinical Chemistry, Charing Cross Hospital, W6 8RF, London, UK.

出版信息

Lancet. 2002 Nov 30;360(9347):1742-5. doi: 10.1016/S0140-6736(02)11683-7.

Abstract

BACKGROUND

Calprotectin (complex of S100A8 and S100A9) is the major calcium and zinc-binding protein of phagocytes. We report a new syndrome with recurrent infections, inflammation, and hyperzincaemia associated with excessively high plasma concentrations of calprotectin.

METHODS

We measured calprotectin in plasma and protein fractions by ELISA assay and zinc by atomic absorption spectrometry. Plasma proteins were fractionated by size exclusion chromatography and electrophoresis. Mass spectra of purified proteins were determined by MALDI-TOFMS.

FINDINGS

We assessed five patients, two of whom are related. All patients had much the same biochemical findings of hyperzincaemia (77-200 micromol/L, reference range 11-18 micromol/L) and raised plasma calprotectin concentrations (1.4-6.5 g/L, reference range <1 mg/L). All patients presented with recurrent infections, hepatosplenomegaly, anaemia, and evidence of systemic inflammation. Three patients had cutaneous inflammation and three presented in infancy with severe growth failure. Size exclusion chromatography showed that zinc and calprotectin were associated in a broad fraction with molecular weight range 100-300 kDa. Analysis by electrophoresis and mass spectrometry showed that the patients' protein contained normal S100A8 and S100A9 subunits.

INTERPRETATION

Dysregulation of zinc metabolism associated with accumulation in plasma of S100A8 and S100A9 defines a new disease, which encompasses a pathological role for dysregulation of two members of the large S100 protein family.

摘要

背景

钙卫蛋白(S100A8和S100A9的复合物)是吞噬细胞中主要的钙和锌结合蛋白。我们报告了一种新的综合征,其特征为反复感染、炎症以及与血浆中钙卫蛋白浓度过高相关的高锌血症。

方法

我们通过ELISA测定法检测血浆和蛋白质组分中的钙卫蛋白,并通过原子吸收光谱法检测锌。血浆蛋白通过尺寸排阻色谱法和电泳进行分离。纯化蛋白的质谱通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOFMS)测定。

研究结果

我们评估了5名患者,其中2名有亲属关系。所有患者都有大致相同的生化检查结果,即高锌血症(77 - 200微摩尔/升,参考范围11 - 18微摩尔/升)和血浆钙卫蛋白浓度升高(1.4 - 6.5克/升,参考范围<1毫克/升)。所有患者均出现反复感染、肝脾肿大、贫血以及全身炎症的证据。3名患者有皮肤炎症,3名患者在婴儿期出现严重生长发育迟缓。尺寸排阻色谱显示锌和钙卫蛋白在分子量范围为100 - 300 kDa的一个宽泛组分中相关联。电泳和质谱分析表明患者的蛋白含有正常的S100A8和S100A9亚基。

解读

与S100A8和S100A9在血浆中蓄积相关的锌代谢失调定义了一种新疾病,其中涉及大型S100蛋白家族两个成员失调的病理作用。

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