Literature DB >> 3693063

Differentiation of the myocardial rudiment of mouse embryos: an ultrastructural study including freeze-fracture replication.

V Navaratnam1, M H Kaufman, J N Skepper, S Barton, K M Guttridge.   

Abstract

The differentiation of the myocardial rudiment was examined in mouse embryos, isolated between the afternoons of the eighth and ninth days of gestation, by means of transmission electron microscopy of ultrathin sections and of freeze-fracture replicas; some of the material used for sectioning was labelled with ruthenium red. Formation of the presumptive pericardial cavity commences during the late presomite stage (afternoon of the eighth day) and the myocardial rudiment originates in situ as a thickening of the splanchnic pericardial lining. Initially, the myocardium comprises an epithelium or plate directly exposed to the pericardial lumen and overlying a separate layer of endocardial elements. As the heart tube bulges into the pericardial coelom, it becomes surrounded by a sleeve of myocardium which thickens and stratifies during the ninth day and subsequently (on the tenth day) acquires an epicardial covering of flattened cells. The myocardium commences pulsations at or about the 3-4 somite stage (morning of the ninth day) by which time the myoblasts already contain striated myofibrillae and specialised cell junctions. From its earliest appearance, the myocardial plate contains tight junctions and desmosomes between the lateral borders of the apical parts of the myoblasts. Gap junctions soon appear in the same regions and they increase in number and extent, as the myoblasts elongate and divide, thus establishing contact in various planes; they are supplemented by the formation of fasciae adherentes and of more desmosomes. On the other hand, tight junctions decline in extent and are eventually confined to the epicardium. Other features such as caveolae and T-tubules are not established by the end of the ninth day and coupling arrangements of the sarcoplasmic reticulum are only in the rudimentary stages of formation.

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Mesh:

Year:  1986        PMID: 3693063      PMCID: PMC1166525     

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  9 in total

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Authors:  R L DEHAAN
Journal:  J Exp Zool       Date:  1964-10

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Authors:  J H Luft
Journal:  Anat Rec       Date:  1971-11

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Authors:  A R Spurr
Journal:  J Ultrastruct Res       Date:  1969-01

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Authors:  S Virágh; C E Challice
Journal:  J Ultrastruct Res       Date:  1973-01

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Authors:  F J Manasek
Journal:  J Embryol Exp Morphol       Date:  1969-11

Review 6.  Junctional intercellular communication: the cell-to-cell membrane channel.

Authors:  W R Loewenstein
Journal:  Physiol Rev       Date:  1981-10       Impact factor: 37.312

7.  Early differentiation of the heart in mouse embryos.

Authors:  M H Kaufman; V Navaratnam
Journal:  J Anat       Date:  1981-09       Impact factor: 2.610

8.  The T-tubule system in the specialized and general myocardium of the rat.

Authors:  A S Ayettey; V Navaratnam
Journal:  J Anat       Date:  1978-09       Impact factor: 2.610

9.  Formation and growth of gap junctions in mouse myocardium during ontogenesis: a freeze-cleave study.

Authors:  D Gros; J P Mocquard; C E Challice; J Schrevel
Journal:  J Cell Sci       Date:  1978-04       Impact factor: 5.285

  9 in total
  12 in total

1.  Development of cardiac musculature in the cranial vena cava of rat embryos.

Authors:  H Endo; K Ogawa; M Kurohmaru; Y Hayashi
Journal:  Anat Embryol (Berl)       Date:  1996-05

2.  Calcium handling precedes cardiac differentiation to initiate the first heartbeat.

Authors:  Richard Cv Tyser; Antonio Ma Miranda; Chiann-Mun Chen; Sean M Davidson; Shankar Srinivas; Paul R Riley
Journal:  Elife       Date:  2016-10-11       Impact factor: 8.140

3.  Tropomyosin is required for cardiac morphogenesis, myofibril assembly, and formation of adherens junctions in the developing mouse embryo.

Authors:  Caroline R McKeown; Roberta B Nowak; David S Gokhin; Velia M Fowler
Journal:  Dev Dyn       Date:  2014-02-24       Impact factor: 3.780

Review 4.  Sca-1+ cardiac progenitor cells and heart-making: a critical synopsis.

Authors:  Mariana Valente; Diana Santos Nascimento; Ana Cumano; Perpétua Pinto-do-Ó
Journal:  Stem Cells Dev       Date:  2014-07-14       Impact factor: 3.272

5.  Observations on the development of the aortico-pulmonary spiral septum in the mouse.

Authors:  K Fananapazir; M H Kaufman
Journal:  J Anat       Date:  1988-06       Impact factor: 2.610

6.  Persistent Noggin arrests cardiomyocyte morphogenesis and results in early in utero lethality.

Authors:  Olga Simmons; Paige Snider; Jain Wang; Robert J Schwartz; Yiping Chen; Simon J Conway
Journal:  Dev Dyn       Date:  2014-12-09       Impact factor: 3.780

7.  Tropomodulin1 is required in the heart but not the yolk sac for mouse embryonic development.

Authors:  Caroline R McKeown; Roberta B Nowak; Jeannette Moyer; Mark A Sussman; Velia M Fowler
Journal:  Circ Res       Date:  2008-10-16       Impact factor: 17.367

8.  Vascular remodeling of the mouse yolk sac requires hemodynamic force.

Authors:  Jennifer L Lucitti; Elizabeth A V Jones; Chengqun Huang; Ju Chen; Scott E Fraser; Mary E Dickinson
Journal:  Development       Date:  2007-09       Impact factor: 6.868

9.  Immunolabelling patterns of gap junction connexins in the developing and mature rat heart.

Authors:  R G Gourdie; C R Green; N J Severs; R P Thompson
Journal:  Anat Embryol (Berl)       Date:  1992

Review 10.  The First Heartbeat-Origin of Cardiac Contractile Activity.

Authors:  Richard C V Tyser; Shankar Srinivas
Journal:  Cold Spring Harb Perspect Biol       Date:  2020-07-01       Impact factor: 9.708

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