Hafke Jens B, Furch Alexandra C U, Reitz Marco U, van Bel Aart J E
Plant Cell Biology Research Group, Institute of General Botany, Justus-Liebig University, D-35390 Giessen, Germany.
Plant Physiol. 2007 Nov;145(3):703-11. doi: 10.1104/pp.107.105940. Epub 2007 Sep 20.
Sieve element (SE) protoplasts were liberated by exposing excised phloem strands of Vicia faba to cell wall-degrading enzyme mixtures. Two types of SE protoplasts were found: simple protoplasts with forisome inclusions and composite twin protoplasts-two protoplasts intermitted by a sieve plate-of which one protoplast often includes a forisome. Forisomes are giant protein inclusions of SEs in Fabaceae. Membrane integrity of SE protoplasts was tested by application of CFDA, which was sequestered in the form of carboxyfluorescein. Further evidence for membrane intactness was provided by swelling of SE protoplasts and forisome dispersion in reaction to abrupt lowering of medium osmolarity. The absence of cell wall remnants as demonstrated by negative Calcofluor White staining allowed patch-clamp studies. At negative membrane voltages, the current-voltage relations of the SE protoplasts were dominated by a weak inward-rectifying potassium channel that was active at physiological membrane voltages of the SE plasma membrane. This channel had electrical properties that are reminiscent of those of the AKT2/3 channel family, localized in phloem cells of Arabidopsis (Arabidopsis thaliana). All in all, SE protoplasts promise to be a powerful tool in studying the membrane biology of SEs with inherent implications for the understanding of long-distance transport and signaling.
通过将蚕豆的韧皮部切段暴露于细胞壁降解酶混合物中来分离筛管分子(SE)原生质体。发现了两种类型的SE原生质体:含有类晶体包涵体的简单原生质体和复合双原生质体(由筛板隔开的两个原生质体,其中一个原生质体通常包含一个类晶体)。类晶体是豆科植物中SE的巨大蛋白质包涵体。通过应用以羧基荧光素形式螯合的CFDA来测试SE原生质体的膜完整性。SE原生质体肿胀以及类晶体在培养基渗透压突然降低时分散,为膜完整性提供了进一步的证据。负性荧光增白剂染色表明不存在细胞壁残余物,这使得能够进行膜片钳研究。在负膜电压下,SE原生质体的电流-电压关系主要由一个弱内向整流钾通道主导,该通道在SE质膜的生理膜电压下具有活性。该通道的电学性质让人联想到定位于拟南芥韧皮部细胞中的AKT2/3通道家族。总之,SE原生质体有望成为研究SE膜生物学的有力工具,这对于理解长距离运输和信号传导具有内在意义。