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防御和黑化依赖于真黑素途径,它们独立发生,并在发育中的地中海实蝇中受到不同的调控。

Defense and melanization depend on the eumelanin pathway, occur independently and are controlled differentially in developing Ceratitis capitata.

作者信息

Charalambidis N D, Bournazos S N, Lambropoulou M, Marmaras V J

机构信息

Department of Biology, University of Patras, Greece.

出版信息

Insect Biochem Mol Biol. 1994 Jul;24(7):655-62. doi: 10.1016/0965-1748(94)90052-3.

Abstract

A defense mechanism in the hemocytes and cuticle of developing Ceratitis capitata has been demonstrated (Marmaras and Charalambidis, 1992; Marmaras et al., 1993a; Marmaras et al., 1993b). To elucidate further the mechanism and the regulation of defense reactions, we studied this process in relation to melanization in the major larval tissues, in two distinct developmental stages; the feeding and wandering larval stages. The results demonstrate that defense reaction depends on reactive tyrosine derivatives of either early or late stages of the sequence of reactions involved in eumelanin biosynthesis. However, defense and melanization occur independently e.g. hemocytes exhibit a high degree of Escherichia coli immobilization and entrapment, but not any ability to biosynthesize melanin. Serum on the other hand, showed a high degree of melanin formation in wandering stage larvae, but had not any ability for E. coli immobilization. In integuments of wandering stage larvae, both processes occur simultaneously. These findings suggest independent control mechanisms for these processes. Indeed, our results suggest that defense seems to be controlled by the presence of proteins responsible for nonself recognition and melanization by developmental regulation of dopachrome conversion factor.

摘要

在发育中的地中海实蝇血细胞和表皮中已证实存在一种防御机制(马尔马拉斯和查拉兰比迪斯,1992年;马尔马拉斯等人,1993年a;马尔马拉斯等人,1993年b)。为了进一步阐明防御反应的机制和调节,我们在两个不同的发育阶段,即取食幼虫阶段和化蛹前幼虫阶段,研究了这一过程与主要幼虫组织中黑化作用的关系。结果表明,防御反应取决于真黑素生物合成相关反应序列早期或晚期的活性酪氨酸衍生物。然而,防御和黑化作用是独立发生的,例如,血细胞表现出高度的大肠杆菌固定和捕获能力,但没有任何生物合成黑色素的能力。另一方面,血清在化蛹前幼虫阶段表现出高度的黑色素形成能力,但没有大肠杆菌固定能力。在化蛹前幼虫的体壁中,这两个过程同时发生。这些发现表明这些过程存在独立的控制机制。事实上,我们的结果表明,防御似乎由负责非自我识别的蛋白质的存在控制,而黑化作用则由多巴色素转换因子的发育调节控制。

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