Morphometric analysis of thoracic aorta in Slc39a13/Zip13-KO mice

Cell Tissue Res. 2019 Apr;376(1):137-141. doi: 10.1007/s00441-018-2977-9. Epub 2019 Jan 4.

Abstract

Ehlers-Danlos syndrome (EDS) is a collection of inheritable diseases involving the musculoskeletal, integumentary and visual systems. Spondylodysplastic EDS-ZIP13 (spEDS-ZIP13: OMIM 612350) was recently defined as a new form of EDS. Although vasculitis has been found in many spEDS-ZIP13 patients, vascular pathology has not been included as a pathognomonic lesion of this type of EDS. We investigate the morphometry of the thoracic aorta in wild-type and Zip13-knockout (Zip13-KO) mice. Our assessment found abnormalities in the number and morphology of elastic and cellular components in the aortic wall, especially the tunica media, of Zip13-KO mice, indicating aortic fragility. Accordingly, our major findings (vascular smooth muscle cells with small nuclei, small percentage of elastic membrane area per tunica media, many large elastic flaps) should be considered vulnerable characteristics indicating fragility of the aorta in patients with spEDS-ZIP13.

Keywords: Aorta; Elastic membrane; Elasticity; Morphometry; Slc39a13/Zip13-KO mouse.

MeSH terms

  • Animals
  • Aorta, Thoracic / abnormalities*
  • Aorta, Thoracic / pathology
  • Cation Transport Proteins / genetics
  • Ehlers-Danlos Syndrome / pathology*
  • Elasticity
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Muscle, Smooth, Vascular / abnormalities*
  • Muscle, Smooth, Vascular / ultrastructure
  • Osteochondrodysplasias / pathology*

Substances

  • Cation Transport Proteins
  • Slc39a13 protein, mouse

Supplementary concepts

  • Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like