[On the mechanism of evagination ofDrosophila imaginai discs culturedin vitro: Effects of substances affecting the cell membrane].

Paul Mandaron
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引用次数: 1

Abstract

The mechanism of evagination of isolated imaginai discs has been studiedin vitro. Pro-, meso-, or metathoracic leg discs were obtained from late 3rd instarDrosophila larvae and cultured in the presence or absence of α-ecdysone and of various substances (cytochalasin B, concanavalin A, neuraminidase, trypsin) known to affect the cell membrane and morphogenetic movements in vertebrates.In the presence of cytochalasin B, evagination was reversibly inhibited. Cytochalasin B apparently does not act on intracellular microfilaments, which could not be detected in the disc cells. It does not prevent ecdysone from being fixed in the cells. It probably modifies the physico-chemical properties of the plasma membrane, precluding the change in cell shape which is required for evagination.In the presence of concanavalin A, which binds specifically to hydroxyl groups of D-mannopyranose or D-glucopyranose, evagination was irreversibly inhibited. The inhibitory effect could however be neutralized by the addition of α-methyl-D-glucopyranose in the medium or prevented by pre-treating the discs in a 0.1% trypsin solution for 2 min.In the presence of neuraminidase, discs evaginated normally under the influence of α-ecdysone; in a few cases, neuraminidase caused partial evagination in the absence of moulting hormone.After treatment by a 0.1% trypsin solution for 2 min, discs evaginated normally under the influence of the moulting hormone; whereas in the absence of ecdysone, evagination was never observed. In the latter case, evagination could however be obtained by a mechanical pull.When normal evagination was inhibited by one of the tested substances, cells did not secrete either a pupal or an imaginai cuticle and did not form any integumentary differentiations.It is concluded that change in cell shape during evagination is related to changes of the cell membrane. The alterations of the physico-chemical properties of the cell membrane, which are required for evagination, are probably caused, during normal development, by the moulting hormone.

[体外培养果蝇囊盘外翻的机制:影响细胞膜物质的作用]。
对离体假椎间盘外翻的机制进行了体外研究。前胸、中胸或后胸腿椎间盘取自3岁晚期果蝇幼虫,并在α-蜕皮素和各种已知影响脊椎动物细胞膜和形态发生运动的物质(细胞松弛素B、豆豆蛋白A、神经氨酸酶、胰蛋白酶)存在或不存在的情况下培养。在细胞松弛素B存在的情况下,外翻被可逆地抑制。细胞松弛素B显然不作用于细胞内微丝,而在盘状细胞中未检测到。它不能阻止蜕皮激素固定在细胞中。它可能改变了质膜的物理化学性质,阻止了细胞形状的改变,而这种改变是体外显影所必需的。在刀豆蛋白A存在的情况下,它可以特异性地与d -甘露吡喃糖或d -葡萄糖吡喃糖的羟基结合,外泄被不可逆地抑制。然而,在培养基中加入α-甲基- d -葡萄糖吡脲可以中和这种抑制作用,或者在0.1%胰蛋白酶溶液中预处理2分钟可以阻止这种抑制作用。在神经氨酸酶存在的情况下,在α-脱皮酮的影响下,椎间盘正常外翻;在少数情况下,神经氨酸酶在没有蜕皮激素的情况下引起部分外翻。经0.1%胰蛋白酶溶液处理2 min后,在蜕皮激素的作用下,椎间盘正常外翻;而在没有蜕皮激素的情况下,从未观察到外翻。在后一种情况下,外翻可以通过机械牵拉获得。当正常外翻被其中一种被测物质抑制时,细胞既不分泌蛹也不分泌想象角质层,也不形成任何表皮分化。由此可见,外翻过程中细胞形态的改变与细胞膜的改变有关。蜕皮所必需的细胞膜的物理化学性质的改变,很可能是在正常发育过程中由蜕皮激素引起的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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