Lang I, Barton D A, Overall R L
School of Biological Sciences, University of Sydney, New South Wales.
Protoplasma. 2004 Dec;224(3-4):231-43. doi: 10.1007/s00709-004-0062-6. Epub 2004 Dec 22.
Field emission scanning electron microscopy of plasmolysed Tradescantia virginiana leaf epidermal cells gave novel insights into the three-dimensional architecture of Hechtian strands, Hechtian reticulum, and the inner surface of the cell wall without the need for extraction. At high magnification, we observed fibres that pin the plasma membrane to the cell wall after plasmolysis. Treatment with cellulase caused these connecting fibres to be lost and the pinned out plasma membrane of the Hechtian reticulum to disintegrate into vesicles with diameters of 100-250 nm. This suggests that the fibres may be cellulose. After 4 h of plasmolysis, a fibrous meshwork that labelled with anti-callose antibodies was observed within the space between the plasmolysed protoplast and the cell wall by field emission scanning electron microscopy. Interestingly, macerase-pectinase treatment resulted in the loss of this meshwork, suggesting that it was stabilised by pectins. We suggest that cellulose microfibrils extending from strands of the Hechtian reticulum and entwining into the cell wall matrix act as anchors for the plasma membrane as it moves away from the wall during plasmolysis.
对质壁分离的紫露草叶片表皮细胞进行场发射扫描电子显微镜观察,无需提取操作就能对赫氏丝、赫氏网以及细胞壁内表面的三维结构有全新的认识。在高倍放大下,我们观察到质壁分离后将质膜固定在细胞壁上的纤维。用纤维素酶处理会导致这些连接纤维消失,赫氏网中固定的质膜解体成直径为100 - 250纳米的囊泡。这表明这些纤维可能是纤维素。质壁分离4小时后,用场发射扫描电子显微镜在质壁分离的原生质体与细胞壁之间的空间内观察到一个用抗胼胝质抗体标记的纤维网络。有趣的是,用离析酶 - 果胶酶处理会导致这个网络消失,这表明它是由果胶稳定的。我们认为,从赫氏网的丝延伸并缠绕到细胞壁基质中的纤维素微纤丝在质壁分离过程中质膜远离细胞壁时起到质膜锚定的作用。