Rothenbusch-Fender Silke, Fritzen Katharina, Bischoff Maik C, Buttgereit Detlev, Oenel Susanne F, Renkawitz-Pohl Renate
Philipps-Universität Marburg, Fachbereich Biologie, Entwicklungsbiologie, Karl-von-Frisch Straße 8, 35043 Marburg, Germany.
DFG Research Training Group, Membrane Plasticity in Tissue Development and Remodeling, GRK 2213, Philipps-Universität Marburg, 35043 Marburg, Germany.
Biol Open. 2017 Dec 15;6(12):1876-1888. doi: 10.1242/bio.025940.
During metamorphosis, nascent testis myotubes migrate from the prospective seminal vesicle of the genital disc onto pupal testes and then further to cover the testes with multinucleated smooth-like muscles. Here we show that DWnt2 is likely required for determination of testis-relevant myoblasts on the genital disc. Knock down of fibroblast growth factor receptor (FGFR) by RNAi and a dominant-negative version revealed multiple functions of Heartless, namely regulation of the amount of myoblasts on the genital disc, connection of seminal vesicles and testes, and migration of muscles along the testes. Live imaging indicated that the downstream effector Stumps is required for migration of testis myotubes on the testis towards the apical tip. After myoblast fusion, myosin II is needed for migration of nascent testis myotubes, in which Thisbe-dependent fibroblast growth factor (FGF) signaling is activated. Cadherin-N is essential for connecting these single myofibers and for creating a firm testis muscle sheath that shapes and stabilizes the testis tubule. Based on these results, we propose a model for the migration of testis myotubes in which nascent testis myotubes migrate as a collective onto and along the testis, dependent on FGF-regulated expression of myosin II.
在变态过程中,新生的睾丸肌管从生殖盘的预期精囊迁移到蛹期睾丸,然后进一步用多核的平滑肌样肌肉覆盖睾丸。在这里,我们表明DWnt2可能是在生殖盘上确定与睾丸相关的成肌细胞所必需的。通过RNA干扰和显性负性版本敲低成纤维细胞生长因子受体(FGFR)揭示了“无情”的多种功能,即调节生殖盘上成肌细胞的数量、精囊与睾丸的连接以及肌肉沿睾丸的迁移。实时成像表明,下游效应器“残端”是睾丸肌管在睾丸上向顶端迁移所必需的。成肌细胞融合后,新生睾丸肌管的迁移需要肌球蛋白II,其中依赖Thisbe的成纤维细胞生长因子(FGF)信号被激活。钙黏蛋白-N对于连接这些单个肌纤维以及形成一个塑造和稳定睾丸小管的坚固睾丸肌肉鞘至关重要。基于这些结果,我们提出了一个睾丸肌管迁移模型,其中新生睾丸肌管作为一个集体迁移到睾丸上并沿着睾丸迁移,这依赖于FGF调节的肌球蛋白II的表达。