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果蝇翅膀成熟过程中的组织重塑。

Tissue remodeling during maturation of the Drosophila wing.

作者信息

Kiger John A, Natzle Jeanette E, Kimbrell Deborah A, Paddy Michael R, Kleinhesselink Kurt, Green M M

机构信息

Section of Molecular and Cellular Biology, University of California, Davis, CA 95616, USA.

出版信息

Dev Biol. 2007 Jan 1;301(1):178-91. doi: 10.1016/j.ydbio.2006.08.011. Epub 2006 Aug 10.

Abstract

The final step in morphogenesis of the adult fly is wing maturation, a process not well understood at the cellular level due to the impermeable and refractive nature of cuticle synthesized some 30 h prior to eclosion from the pupal case. Advances in GFP technology now make it possible to visualize cells using fluorescence after cuticle synthesis is complete. We find that, between eclosion and wing expansion, the epithelia within the folded wing begin to delaminate from the cuticle and that delamination is complete when the wing has fully expanded. After expansion, epithelial cells lose contact with each other, adherens junctions are disrupted, and nuclei become pycnotic. The cells then change shape, elongate, and migrate from the wing into the thorax. During wing maturation, the Timp gene product, tissue inhibitor of metalloproteinases, and probably other components of an extracellular matrix are expressed that bond the dorsal and ventral cuticular surfaces of the wing following migration of the cells. These steps are dissected using the batone and Timp genes and ectopic expression of alphaPS integrin, inhibitors of Armadillo/beta-catenin nuclear activity and baculovirus caspase inhibitor p35. We conclude that an epithelial-mesenchymal transition is responsible for epithelial delamination and dissolution.

摘要

成年果蝇形态发生的最后一步是翅膀成熟,由于在从蛹壳羽化前约30小时合成的角质层具有不可渗透和折射的特性,这一过程在细胞水平上尚未得到很好的理解。绿色荧光蛋白(GFP)技术的进步现在使得在角质层合成完成后利用荧光观察细胞成为可能。我们发现,在羽化和翅膀展开之间,折叠翅膀内的上皮细胞开始从角质层分层,并且当翅膀完全展开时分层完成。展开后,上皮细胞彼此失去接触,黏着连接被破坏,细胞核固缩。然后细胞改变形状,伸长并从翅膀迁移到胸部。在翅膀成熟过程中,金属蛋白酶组织抑制剂(Timp)基因产物以及可能的细胞外基质的其他成分会表达,这些成分在细胞迁移后将翅膀的背侧和腹侧角质层表面结合在一起。利用batone和Timp基因以及αPS整合素的异位表达、犰狳蛋白/β-连环蛋白核活性抑制剂和杆状病毒半胱天冬酶抑制剂p35对这些步骤进行了剖析。我们得出结论,上皮-间质转化是上皮分层和溶解的原因。

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