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MPTP 对体外灵长类嗜铬细胞的影响:与肾上腺髓质细胞移植的相关性。

Effect of MPTP on primate chromaffin cells in vitro: relevance for adrenal medullary cell transplantation.

机构信息

Department of Neurobiology and Anatomy, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642 (U.S.A.).

出版信息

Restor Neurol Neurosci. 1991 Jan 1;3(1):1-10. doi: 10.3233/RNN-1991-3101.

Abstract

Primate adrenal medullary cells were exposed to l-methyl-4-phenyl-l,2,3,6-tetrahydropyridine (MPTP) in vitro to examine the effect of this neurotoxic agent on chromaffin cells. Chromaffin cells from monkey and humans were cultured in the presence of 100 ng/ml nerve growth factor for 1 week and then exposed to 150 μM MPTP or its active metabolite methylpyridinium ion (MPP+) for an additional week. Cells which had extended neurites in the presence of NGF showed no morphological effect in response to MPTP or MPP+ at the light microscopic level. However, there was a significant loss in catecholamines as seen by histofluorescence and high performance liquid chromotography (HPLC). Electron microscopy revealed a depletion in dense-core vesicles in chromaffin cells after chronic exposure to MPTP while the mitochondria appeared similar to those observed in control cells. Replacement of MPTP medium with standard medium stimulated restoration of catecholamine histofluorescence after 7 days. An acute 15 min pretreatment of chromaffin cells with MPTP or MPP+ induced secretion of catecholamines over a 1 h pulse, with MPP+ producing the maximum and more rapid secretion as determined by HPLC. These data indicate that MPTP induces a dramatic loss in catecholamines in primate chromaffin cells in vitro after both acute and chronic exposures; however, removal of the toxic agent permits restoration of catecholamines without permanent effect on the integrity of these cells.

摘要

原代灵长类肾上腺髓质细胞在体外接触 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP),以研究这种神经毒性物质对嗜铬细胞的影响。猴子和人类的嗜铬细胞在 100ng/ml 神经生长因子存在的情况下培养 1 周,然后再暴露于 150μM MPTP 或其活性代谢物甲基吡啶鎓离子(MPP+)1 周。在 NGF 存在下具有延伸轴突的细胞在 MPTP 或 MPP+的作用下,在光镜水平上没有形态学效应。然而,通过组织荧光和高效液相色谱(HPLC)观察到儿茶酚胺有明显的丢失。电镜显示,在慢性暴露于 MPTP 后,嗜铬细胞中的致密核心囊泡耗竭,而线粒体与对照细胞中观察到的相似。用标准培养基替换 MPTP 培养基可刺激儿茶酚胺组织荧光在 7 天后恢复。用 MPTP 或 MPP+急性预处理 15 分钟,可诱导儿茶酚胺在 1 小时脉冲中分泌,HPLC 测定结果显示 MPP+产生的分泌量最大且更快。这些数据表明,MPTP 在体外急性和慢性暴露后均可导致灵长类嗜铬细胞中儿茶酚胺的显著丢失;然而,去除毒性物质可恢复儿茶酚胺,而对这些细胞的完整性没有永久影响。

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