Literature DB >> 19048632

Micro-CT evaluation of murine fetal skeletal development yields greater morphometric precision over traditional clear-staining methods.

Megan E Oest1, Jeryl C Jones, Cindy Hatfield, M Renee Prater.   

Abstract

Traditional techniques for quantification of murine fetal skeletal development (gross measurements, clear-staining) are severely limited by specimen processing, soft tissue presence, diffuse staining, and unclear landmarks between which to make measurements. Nondestructive microcomputed tomography (micro-CT) imaging is a versatile, well-documented tool traditionally used to generate high-resolution 3-D images and quantify microarchitectural parameters of trabecular bone. Although previously described as a tool for phenotyping fetal murine specimens, micro-CT has not previously been used to directly measure individual fetal skeletal structures. Imaging murine fetal skeletons using micro-CT enables the researcher to nondestructively quantify fetal skeletal development parameters including limb length, total bone volume, and average bone mineral density, as well as identify skeletal malformations. Micro-CT measurement of fetal limb lengths correlates well with traditional clear-staining methods (83.98% agreement), decreases variability in measurements (average standard errors: 6.28% for micro-CT and 10.82% for clear-staining), decreases data acquisition time by eliminating the need for tissue processing, and preserves the intact fixed fetus for further analysis. Use of the rigorous micro-CT technique to generate 3-D images for digital measurement enables isolation of skeletal structures based on degree of mineralization (local radiodensity), eliminating the complications of blurred stain boundaries and soft tissue inclusion that accompany clear-staining and gross measurement techniques. Microcomputed tomography provides a facile, accurate, and nondestructive method for determining the developmental state of the fetal skeleton using not only limb lengths and identification of malformations, but total skeletal bone volume and average skeletal mineral density as well.

Entities:  

Mesh:

Year:  2008        PMID: 19048632     DOI: 10.1002/bdrb.20177

Source DB:  PubMed          Journal:  Birth Defects Res B Dev Reprod Toxicol        ISSN: 1542-9733


  5 in total

1.  A correlative method for imaging identical regions of samples by micro-CT, light microscopy, and electron microscopy: imaging adipose tissue in a model system.

Authors:  Gerhard Sengle; Sara F Tufa; Lynn Y Sakai; Martin A Zulliger; Douglas R Keene
Journal:  J Histochem Cytochem       Date:  2012-12-20       Impact factor: 2.479

2.  Real time observation of mouse fetal skeleton using a high resolution X-ray synchrotron.

Authors:  Dong Woo Chang; Bora Kim; Jae Hoon Shin; Young Min Yun; Jung Ho Je; Yeu Kuang Hwu; Jung Hee Yoon; Je Kyung Seong
Journal:  J Vet Sci       Date:  2011-06       Impact factor: 1.672

3.  Quantitative in vivo micro-computed tomography for assessment of age-dependent changes in murine whole-body composition.

Authors:  Kim L Beaucage; Steven I Pollmann; Stephen M Sims; S Jeffrey Dixon; David W Holdsworth
Journal:  Bone Rep       Date:  2016-04-09

4.  Cranial asymmetry arises later in the life history of the blind Mexican cavefish, Astyanax mexicanus.

Authors:  Amanda K Powers; Erin M Davis; Shane A Kaplan; Joshua B Gross
Journal:  PLoS One       Date:  2017-05-09       Impact factor: 3.240

Review 5.  Mouse embryo phenotyping using X-ray microCT.

Authors:  Stephan Handschuh; Martin Glösmann
Journal:  Front Cell Dev Biol       Date:  2022-09-16
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.