Branching morphogenesis in the developing kidney is governed by rules that pattern the ureteric tree

Development. 2017 Dec 1;144(23):4377-4385. doi: 10.1242/dev.153874. Epub 2017 Oct 16.

Abstract

Metanephric kidney development is orchestrated by the iterative branching morphogenesis of the ureteric bud. We describe an underlying patterning associated with the ramification of this structure and show that this pattern is conserved between developing kidneys, in different parts of the organ and across developmental time. This regularity is associated with a highly reproducible branching asymmetry that is consistent with locally operative growth mechanisms. We then develop a class of tip state models to represent elaboration of the ureteric tree and describe rules for 'half-delay' branching morphogenesis that describe almost perfectly the patterning of this structure. Spatial analysis suggests that the observed asymmetry may arise from mutual suppression of bifurcation, but not extension, between the growing ureteric tips, and demonstrates that disruption of patterning occurs in mouse mutants in which the distribution of tips on the surface of the kidney is altered. These findings demonstrate that kidney development occurs by way of a highly conserved reiterative pattern of asymmetric bifurcation that is governed by intrinsic and locally operative mechanisms.

Keywords: Branching morphogenesis; Mathematical modelling; Ureteric tree.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / deficiency
  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / physiology
  • Animals
  • Body Patterning / genetics
  • Body Patterning / physiology
  • Bone Morphogenetic Protein 7 / deficiency
  • Bone Morphogenetic Protein 7 / genetics
  • Bone Morphogenetic Protein 7 / physiology
  • Imaging, Three-Dimensional
  • Kidney / embryology*
  • Mathematical Concepts
  • Membrane Proteins / deficiency
  • Membrane Proteins / genetics
  • Membrane Proteins / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Mutant Strains
  • Models, Biological
  • Morphogenesis / genetics
  • Morphogenesis / physiology*
  • Mutation
  • Phenotype
  • Phosphoproteins / deficiency
  • Phosphoproteins / genetics
  • Phosphoproteins / physiology
  • Transforming Growth Factor beta2 / deficiency
  • Transforming Growth Factor beta2 / genetics
  • Transforming Growth Factor beta2 / physiology
  • Ureter / embryology*

Substances

  • Adaptor Proteins, Signal Transducing
  • Bone Morphogenetic Protein 7
  • Membrane Proteins
  • Phosphoproteins
  • Spry1 protein, mouse
  • Tgfb2 protein, mouse
  • Transforming Growth Factor beta2
  • bmp7 protein, mouse