The Effects of Indian Hedgehog Deletion on Mesenchyme Cells: Inducing Intermediate Cartilage Scaffold Ossification to Cause Growth Plate and Phalange Joint Absence, Short Limb, and Dwarfish Phenotypes

Stem Cells Dev. 2018 Oct 15;27(20):1412-1425. doi: 10.1089/scd.2018.0071. Epub 2018 Aug 22.

Abstract

The endochondral ossification plays a critical role in vertebrate limb development and skeletal homeostasis, where limb mesenchyme cells form an intermediate cartilage scaffold that develops into growth plates and then replaced by bone. Although Indian hedgehog (Ihh) is known to control the hypertrophic differentiation process of chondrocytes, its role from the mesenchyme cells to the early stages of chondrogenesis is unclear. To define the function of Ihh in the mesenchymal cell's early stages of chondrogenesis, we specifically delete Ihh in Prx1-expressed mesenchyme cells at E9.5 using Prx1-Cre;Ihhfl/fl;Rosa26-ZsGreen1 mice. We found that deleting Ihh in the mesenchyme cells results in an early and quick ossification of the intermediate cartilage scaffold, causing the growth plate and phalange joint absence, short limbs, and dwarfishness. The green fluorescent protein (GFP)-positive cells derived from deleted Ihh mesenchyme cells overlap with von Kossa- and osteocalcin-positive staining area. These deleted Ihh/GFP-positive cells isolated from Prx1-Cre;Ihhfl/fl;Rosa26-ZsGreen1 newborn mice had osteogenic differentiation by showing a positive Alizarin red and von Kossa staining, as well as an enhanced Col1a1, osteocalcin, and Runx2 expression. Our findings demonstrate that deleting Ihh in mesenchyme cells during early limb development promotes intermediate cartilage scaffold ossification, which prevents growth plate formation that causes phalange joint absence, short limb, and dwarfish phenotype.

Keywords: Indian hedgehog; hypertrophic chondrocytes; mesenchymal cells; synovial joint.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Development / genetics*
  • Cartilage / growth & development
  • Chondrogenesis / genetics
  • Dwarfism / genetics
  • Dwarfism / physiopathology
  • Extremities / growth & development
  • Extremities / pathology
  • Gene Expression Regulation, Developmental / genetics
  • Growth Plate / growth & development*
  • Growth Plate / metabolism
  • Growth Plate / pathology
  • Hedgehog Proteins / genetics*
  • Homeodomain Proteins / genetics*
  • Humans
  • Mesenchymal Stem Cells / cytology*
  • Mice
  • Osteogenesis / genetics
  • Phalangeridae / genetics
  • Phalangeridae / growth & development
  • Vertebrates / genetics
  • Vertebrates / growth & development

Substances

  • Hedgehog Proteins
  • Homeodomain Proteins
  • Prrx1 protein, mouse
  • ihh protein, mouse