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硫酸盐限制对海洋海绵微拟海棉的生化及功能影响

Biochemical and Functional Effects of Sulfate Restriction in the Marine Sponge, Microciona prolifera.

作者信息

Kuhns W J, Misevic G, Burger M M

出版信息

Biol Bull. 1990 Dec;179(3):358-365. doi: 10.2307/1542328.

DOI:10.2307/1542328
PMID:29314967
Abstract

The functional and biochemical consequences of sulfate restriction were studied in chemically dissociated Microciona sponge cells maintained in artificial seawater with or without SO42-. In cells pre-treated to reduce preformed secretions, SO42- deprivation reduced cell motility judged by the lack of aggregates in rotating or stationary cultures in comparison with controls. Microscopic examination showed that cells that customarily demonstrate cytoplasmic processes, such as filopodia and pseudopodia, exhibited marked decreases in these cellular processes when maintained in SO42--deprived artificial seawater. Uptake and incorporation of 35SO42- by disaggregated and pre-treated cells was higher under SO42--free conditions relative to controls; this effect was time dependent, rising to a maximum at 12 h, when a three- to seven-fold difference could be demonstrated. 3H-leucine incorporation indicated that protein synthesis was similar in test and control populations. Comparative high voltage electrophoresis of supernatants containing 35SO4 macromolecules from chemically dissociated cells indicated deficiencies of such 35SO4 macromolecules if the rotated cells that released these secretions had been pre-treated in SO42--free artificial seawater. The results of SO42- restriction suggest that secretion of macromolecules or Microciona aggregation factor (MAF), and aggregation and locomotion of Microciona cells depend upon an adequate extracellular source of SO42-, sulfate transport, and sulfation of macromolecules such as polysaccharides.

摘要

在含有或不含SO42-的人工海水中维持化学解离的微小海绵细胞,研究了硫酸盐限制的功能和生化后果。在预先处理以减少预先形成的分泌物的细胞中,与对照相比,通过旋转或静止培养中缺乏聚集体判断,SO42-剥夺降低了细胞运动性。显微镜检查显示,通常表现出细胞质突起(如丝状伪足和伪足)的细胞,当维持在缺乏SO42-的人工海水中时,这些细胞过程显著减少。相对于对照,在无SO42-条件下,解离和预处理细胞对35SO42-的摄取和掺入更高;这种效应是时间依赖性的,在12小时时达到最大值,此时可显示出三到七倍的差异。3H-亮氨酸掺入表明测试组和对照组的蛋白质合成相似。对来自化学解离细胞含有35SO4大分子的上清液进行的比较高压电泳表明,如果释放这些分泌物的旋转细胞在无SO42-的人工海水中进行预处理,则此类35SO4大分子存在缺陷。SO42-限制的结果表明,大分子或微小海绵聚集因子(MAF)的分泌以及微小海绵细胞的聚集和运动取决于足够的细胞外SO42-来源、硫酸盐转运以及多糖等大分子的硫酸化作用。

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