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铅暴露导致红系祖细胞剂量依赖性减少及促红细胞生成素反应异常:铅致贫血的新机制

Dose dependent reduction of erythroid progenitor cells and inappropriate erythropoietin response in exposure to lead: new aspects of anaemia induced by lead.

作者信息

Osterode W, Barnas U, Geissler K

机构信息

Universitätsklinik für Innere Medizin IV, Klinische Abteilung für Arbeitsmedizm, Wien, Austria.

出版信息

Occup Environ Med. 1999 Feb;56(2):106-9. doi: 10.1136/oem.56.2.106.

Abstract

OBJECTIVE

To determine whether haematopoietic progenitor cells and erythropoietin (EPO), which is an essential humoral stimulus for erythroid progenitor (BFU-E) cell differentiation, are affected by lead intoxication.

METHODS

In male subjects chronically exposed to lead with and without anaemia, pluripotent (CFU-GEMM), BFU-E and granulocyte/macrophage (CFU-GM) progenitor cell counts in peripheral blood were measured with a modified clonal assay. Lead concentrations in blood (PbB) and urine (PbU) were measured by the atomic absorption technique, and EPO was measured with a modified radioimmunoassay.

RESULTS

PbB in the subjects exposed to lead ranged from 0.796 to 4.4 mumol/l, and PbU varied between 0.033 and 0.522 mumol/l. In subjects exposed to lead with PbB > or = 2.896 mumol/l (n = 7), BFU-E cells were significantly reduced (p < 0.001) whereas the reduction in CFU-GM cells was only of borderline significance (p = 0.037) compared with the age matched controls (n = 20). The CFU-GEMM cells remained unchanged. Furthermore, BFU-E and CFU-GM cells were reduced in a dose dependent fashion, with increasing PbB or PbU, respectively. In the subjects exposed to lead EPO was in the normal range and did not increase in the presence of anaemia induced by lead. No correlations existed between EPO and PbB, PbU, or progenitor cells.

CONCLUSION

The data suggest new aspects of lead induced anaemia besides the currently acknowledged shortened life span of erythrocytes and inhibition of haemoglobin synthesis. Two additional mechanisms should be considered: the reduction of BFU-E cells, and inappropriate renal EPO production in the presence of severe exposure to lead, which would lead to an inadequate maturation of BFU-E cells.

摘要

目的

确定造血祖细胞和促红细胞生成素(EPO)是否受铅中毒影响,EPO是红系祖细胞(BFU-E)分化所必需的体液刺激因子。

方法

对有或无贫血的慢性铅暴露男性受试者,采用改良克隆分析法检测外周血中多能(CFU-GEMM)、BFU-E和粒细胞/巨噬细胞(CFU-GM)祖细胞计数。采用原子吸收技术测定血铅(PbB)和尿铅(PbU)浓度,采用改良放射免疫分析法测定EPO。

结果

铅暴露受试者的PbB范围为0.796至4.4μmol/L,PbU在0.033至0.522μmol/L之间。在PbB≥2.896μmol/L的铅暴露受试者中(n = 7),与年龄匹配的对照组(n = 20)相比,BFU-E细胞显著减少(p < 0.001),而CFU-GM细胞的减少仅具有临界显著性(p = 0.037)。CFU-GEMM细胞保持不变。此外,BFU-E和CFU-GM细胞分别随着PbB或PbU的增加呈剂量依赖性减少。铅暴露受试者的EPO在正常范围内,且在铅诱导的贫血情况下未升高。EPO与PbB、PbU或祖细胞之间无相关性。

结论

数据提示,除了目前公认的红细胞寿命缩短和血红蛋白合成受抑制外,铅诱导贫血还有新的方面。应考虑另外两种机制:BFU-E细胞减少,以及在严重铅暴露情况下肾脏EPO产生不当,这将导致BFU-E细胞成熟不足。

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