Literature DB >> 19359541

Histology atlas of the developing mouse heart with emphasis on E11.5 to E18.5.

Saija M Savolainen1, Julie F Foley, Susan A Elmore.   

Abstract

In humans, congenital heart diseases are common. Since the rapid progression of transgenic technologies, the mouse has become the major animal model of defective cardiovascular development. Moreover, genetically modified mice frequently die in utero, commonly due to abnormal cardiovascular development. A variety of publications address specific developmental stages or structures of the mouse heart, but a single reference reviewing and describing the anatomy and histology of cardiac developmental events, stage by stage, has not been available. The aim of this color atlas, which demonstrates embryonic/fetal heart development, is to provide a tool for pathologists and biomedical scientists to use for detailed histological evaluation of hematoxylin and eosin (H&E)-stained sections of the developing mouse heart with emphasis on embryonic days (E) 11.5-18.5. The selected images illustrate the main structures and developmental events at each stage and serve as reference material for the confirmation of the chronological age of the embryo/early fetus and assist in the identification of any abnormalities. An extensive review of the literature covering cardiac development pre-E11.5 is summarized in the introduction. Although the focus of this atlas is on the descriptive anatomic and histological development of the normal mouse heart from E11.5 to E18.5, potential embryonic cardiac lesions are discussed with a list of the most common transgenic pre- and perinatal heart defects. Representative images of hearts at E11.5-15.5 and E18.5 are provided in Figures 2-4, 6, 8, and 9. A complete set of labeled images (Figures E11.5-18.5) is available on the CD enclosed in this issue of Toxicologic Pathology. All digital images can be viewed online at https://niehsimages.epl-inc.com with the username "ToxPath" and the password "embryohearts."

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Year:  2009        PMID: 19359541      PMCID: PMC2773446          DOI: 10.1177/0192623309335060

Source DB:  PubMed          Journal:  Toxicol Pathol        ISSN: 0192-6233            Impact factor:   1.902


  62 in total

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  57 in total

1.  Endothelial alpha5 and alphav integrins cooperate in remodeling of the vasculature during development.

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Review 2.  Cardiac developmental toxicity.

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3.  Ablation of Nkx2-5 at mid-embryonic stage results in premature lethality and cardiac malformation.

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4.  Activation of multiple signaling pathways causes developmental defects in mice with a Noonan syndrome–associated Sos1 mutation.

Authors:  Peng-Chieh Chen; Hiroko Wakimoto; David Conner; Toshiyuki Araki; Tao Yuan; Amy Roberts; Christine E Seidman; Roderick Bronson; Benjamin G Neel; Jonathan G Seidman; Raju Kucherlapati
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5.  Drosophila Preparation and Longitudinal Imaging of Heart Function In Vivo Using Optical Coherence Microscopy (OCM).

Authors:  Jing Men; Jason Jerwick; Penghe Wu; Mingming Chen; Aneesh Alex; Yutao Ma; Rudolph E Tanzi; Airong Li; Chao Zhou
Journal:  J Vis Exp       Date:  2016-12-12       Impact factor: 1.355

6.  A mouse model of human congenital heart disease: high incidence of diverse cardiac anomalies and ventricular noncompaction produced by heterozygous Nkx2-5 homeodomain missense mutation.

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Journal:  Circ Cardiovasc Genet       Date:  2014-07-15

7.  Myostatin regulates tissue potency and cardiac calcium-handling proteins.

Authors:  Melissa F Jackson; Naisi Li; Buel D Rodgers
Journal:  Endocrinology       Date:  2014-02-11       Impact factor: 4.736

8.  The Src homology and collagen A (ShcA) adaptor protein is required for the spatial organization of the costamere/Z-disk network during heart development.

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Authors:  Rinat Gabbay-Benziv; E Albert Reece; Fang Wang; Amnon Bar-Shir; Chris Harman; Ozhan M Turan; Peixin Yang; Sifa Turan
Journal:  Magn Reson Imaging       Date:  2016-08-26       Impact factor: 2.546

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Journal:  Nucleic Acids Res       Date:  2009-12       Impact factor: 16.971

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