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[关于体外培养的果蝇成虫盘外翻的机制:影响细胞膜的物质的作用]

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

作者信息

Mandaron Paul

机构信息

Laboratoire de Zoologie de l'Université Scientifique et Médicale de Grenoble, France.

出版信息

Wilhelm Roux Arch Entwickl Mech Org. 1974 Mar;175(1):49-63. doi: 10.1007/BF00573223.

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.

摘要

已在体外研究了离体成虫盘外翻的机制。从三龄晚期果蝇幼虫中获取前胸、中胸或后胸腿盘,并在有或没有α -蜕皮激素以及已知会影响脊椎动物细胞膜和形态发生运动的各种物质(细胞松弛素B、伴刀豆球蛋白A、神经氨酸酶、胰蛋白酶)存在的情况下进行培养。在细胞松弛素B存在时,外翻被可逆性抑制。细胞松弛素B显然不作用于盘细胞中未检测到的细胞内微丝。它并不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,排除了外翻所需的细胞形状变化。在伴刀豆球蛋白A存在时,它特异性结合D -甘露吡喃糖或D -葡糖吡喃糖的羟基,外翻被不可逆地抑制。然而,通过在培养基中添加α -甲基 - D -葡糖吡喃糖可以中和这种抑制作用,或者通过将盘在0.1%胰蛋白酶溶液中预处理2分钟来防止。在神经氨酸酶存在时,盘在α -蜕皮激素的影响下正常外翻;在少数情况下,神经氨酸酶在没有蜕皮激素的情况下导致部分外翻。用0.1%胰蛋白酶溶液处理2分钟后,盘在蜕皮激素的影响下正常外翻;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,然而通过机械牵拉可以实现外翻。当正常外翻被所测试物质之一抑制时,细胞既不分泌蛹皮或成虫皮,也不形成任何体表分化。得出的结论是,外翻过程中的细胞形状变化与细胞膜的变化有关。外翻所需的细胞膜物理化学性质的改变,在正常发育过程中可能是由蜕皮激素引起的。

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