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Erythrocytes in the endocardial structures of embryonic heart

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Mashtalir M.A., Lapsar A.S. Erythrocytes in the endocardial structures of embryonic heart.

Summary. With the purpose to study the phenomenon of erythrocyte migration into the endocardial structures of the embryo

heart the serial sections of chick embryos of white leghorn and Cobb 500 cross on 68, 72, 76, 80 and 96 hours of incubation were studied in light microscope. Erythrocytes, freely arranged in the cardiac jelly of conotrunkal cushions, were a frequent finding on 72 hours (stage 20 by V.Hamburger, H.L.Hamilton, 1951). Endocardially disposed erythrocytes were adjoined to transformed endothelial cells which started to migrate into the cardiac jelly. Morphological pictures show that erythrocytes migrate via diapedesis through endocardail endothelium. Erythrocytes were also encountered distant from endocardium, sometimes close by the myocardium of conotrunkal region. These erythrocytes may get to the cardiac jelly by another way. The pictures of deformation of erythrocytes observed in the cardiac jelly show the further dying of these cells. If the incuba-tion time was less than 72 hours, and later, on 76 and 80 hours of incubaincuba-tion, erythrocytes were rarely found in the cardiac jelly of endocardial cushions. We consider the investigated phenomenon is determined by a transient, expected in certain stages, status of endocardial endothelial cells, which may relate with epithelial-mesenchymal transformation.

Key words: endocardial cushions, epithelial-mesenchymal transformation, erythrocytes, embryo heart, diapedesis.

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Dosage-dependent effects of Akt1/protein kinase Balpha (PKBalpha) and Akt3/PKBgamma on thymus, skin, and cardiovascular and nervous sys-tem development in mice / Z. Z. Yang, O. Tschopp, N. Di-Poi [et al.] // Mol. Cell. Biol. – 2005. – Vol. 25, № 23. – P. 10407-10418.

Epicardium-derived cells contribute a novel population to the myocardial wall and the atrioven-tricular cushions / Adriana C. Gittenberger-de Groot, Mark-Paul F. M. Vrancken Peeters, Monica M. T. Mentink [et al.] // Circ. Res. – 1998. – Vol. 82. – P. 1043-1052.

Expression patterns of Tgfβ1-3 associate with myocardialisation of the outflow tract and the devel-opment of the epicardium and the fibrous heart skeleton / D. G. Molin, U. Bartram, K. Van der Hei-den [et al.] // Dev. Dyn. – 2003. – Vol. 227, № 3. – P. 431-444.

FGF-16 is required for embryonic heart devel-opment / Shun Yan Lu, Farah Sheikh, Patricia C. Sheppard [et al.] // Biochem. Biophys. Res. Com-mun. – Vol. 373, № 2. – P. 270-274.

Hamburger V. A series of normal stages in the development of the chick embryo / Viktor Ham-burger, Howard L. Hamilton // J. Morphol. – 1951. - Vol. 88, № 1. – . 49-92.

Hutson M. R. Neural crest and cardiovascular development: a 20-year perspective / Hutson M. R., Kirby M. L. // Birth Defects Res. C. Embryo Today. – 2003. – Vol. 69, № 1. – P. 2-13.

Kattan J. Formation and remodeling of the coronary vascular bed in the embryonic avian heart / Javier Kattan, Robert W. Dettman, James Bristow // Dev Dyn. – 2004. – Vol. 230. – P. 34–43.

Markarian M. Type and frequency of malfor-mations in chick embryos / Markarian M. // Vet. Med. Nauki. – 1978. – Vol. 15, № 4. – P. 40-44.

RDH10 is essential for synthesis of embryonic retinoic acid and is required for limb, craniofacial, and organ development / Lisa L. Sandell, Brian W. Sanderson, Gennadiy Moiseyev [et al.] // Genes Dev. – 2007. – Vol. 21. - P. 1113-1124.

Tomanek R. J. Vascular patterning of the quail coronary system during development / Robert J. Tomanek, Heidi K. Hansen, Eduard I. Dedkov // Anat. Rec. – 2006. – Vol. 288A. – P. 989-999.

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