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Image-based modeling of kidney branching morphogenesis reveals GDNF-RET based Turing-type mechanism and pattern-modulating WNT11 feedback

机译:肾脏分支形态发生的基于图像的建模揭示了基于GDNF-RET的图灵型机制和模式调节WNT11反馈

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摘要

Branching patterns and regulatory networks differ between branched organs. It has remained unclear whether a common regulatory mechanism exists and how organ-specific patterns can emerge. Of all previously proposed signalling-based mechanisms, only a ligand-receptor-based Turing mechanism based on FGF10 and SHH quantitatively recapitulates the lung branching patterns. We now show that a GDNF-dependent ligand-receptor-based Turing mechanism quantitatively recapitulates branching of cultured wildtype and mutant ureteric buds, and achieves similar branching patterns when directing domain outgrowth in silico. We further predict and confirm experimentally that the kidney-specific positive feedback between WNT11 and GDNF permits the dense packing of ureteric tips. We conclude that the ligand-receptor based Turing mechanism presents a common regulatory mechanism for lungs and kidneys, despite the differences in the molecular implementation. Given its flexibility and robustness, we expect that the ligand-receptor-based Turing mechanism constitutes a likely general mechanism to guide branching morphogenesis and other symmetry breaks during organogenesis.
机译:分支机构之间的分支模式和调节网络不同。尚不清楚是否存在共同的调节机制,以及如何出现器官特异性模式。在所有先前提出的基于信号传导的机制中,只有基于FGF10和SHH的基于配体受体的图灵机制可定量地概括肺分支模式。我们现在显示,基于GDNF的配体受体为基础的图灵机制定量地概括了培养的野生型和突变输尿管芽的分支,并在计算机中指导域扩展时达到了相似的分支模式。我们进一步预测和实验证实,WNT11和GDNF之间的肾脏特异性正反馈允许输尿管尖端的密集堆积。我们得出结论,尽管在分子实施方式上存在差异,但基于配体-受体的图灵机制为肺和肾脏提供了一种常见的调节机制。鉴于其灵活性和鲁棒性,我们期望基于配体-受体的图灵机制构成可能的一般机制,以指导器官发生过程中的分支形态发生和其他对称性断裂。

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