Location and growth of epaxial myotome precursor cells

Development ◽  
1997 ◽  
Vol 124 (8) ◽  
pp. 1601-1610 ◽  
Author(s):  
W.F. Denetclaw ◽  
B. Christ ◽  
C.P. Ordahl
Keyword(s):  
Skeletal Muscle ◽  
Confocal Microscopy ◽  
Embryonic Development ◽  
Progenitor Cells ◽  
Neural Tube ◽  
Precursor Cells ◽  
Dorsal Region ◽  
In Ovo ◽  
Close Proximity ◽  
Inducing Factors

The skeletal muscle progenitor cells of the vertebrate body originate in the dermomyotome epithelium of the embryonic somites. To precisely locate myotome precursor cells, fluorescent vital dyes were iontophoretically injected at specific sites in the dermomyotome in ovo and the fates of dye-labeled cells monitored by confocal microscopy. Dye-labeled myotome myofibers were generated from cells injected along the entire medial boundary and the medial portion of the cranial boundary of the dermomyotome, regions in close proximity to the dorsal region of the neural tube where myogenic-inducing factors are thought to be produced. Other injected regions of the dermomyotome did not give rise to myotome fibers. Analysis of nascent myotome fibers showed that they elongate along the embryonic axis in cranial and caudal directions, or in both directions simultaneously, until they reach the margins of the dermomyotome. Finally, deposition of myotome fibers and expansion of the dermomyotome epithelium occurs in a lateral-to-medial direction. This new model for early myotome formation has implications for myogenic specification and for growth of the epaxial domain during early embryonic development.

scholarly journals Effects of In-Ovo injection of Biotin on chick’s embryonic development and physiological traits

2021 ◽  
Vol 761 (1) ◽  
pp. 012111
Author(s):  
S. A. Alkubaisy ◽  
A. A. Majid ◽  
S. M. Abdulateef ◽  
F. A. Al-Bazy ◽  
O. K. Attallah ◽  
...  
Keyword(s):  
Embryonic Development ◽  
Physiological Traits ◽  
In Ovo ◽  
In Ovo Injection

Confocal microscopy study of membrane organelles of the skeletal muscle fiber in the process of Zenker’s (spreading) necrosis

2007 ◽  
Vol 1 (2) ◽  
pp. 183-190 ◽  
Author(s):  
S. A. Krolenko ◽  
S. Ya. Adamyan ◽  
T. N. Belyaeva ◽  
T. P. Mozhenok ◽  
A. V. Salova
Keyword(s):  
Skeletal Muscle ◽  
Confocal Microscopy ◽  
Muscle Fiber ◽  
Microscopy Study ◽  
Skeletal Muscle Fiber

scholarly journals Neural Progenitor Cells Undergoing Yap/Tead-Mediated Enhanced Self-Renewal Form Heterotopias More Easily in the Diencephalon than in the Telencephalon

2018 ◽  
Vol 43 (1) ◽  
pp. 180-189 ◽  
Author(s):  
Kanako Saito ◽  
Ryotaro Kawasoe ◽  
Hiroshi Sasaki ◽  
Ayano Kawaguchi ◽  
Takaki Miyata
Keyword(s):  
Progenitor Cells ◽  
Neural Tube ◽  
Neural Progenitor Cells ◽  
Three Dimensional ◽  
Neural Progenitor ◽  
Hippo Signaling ◽  
Apical Surface ◽  
Elevated Expression ◽  
Underlying Mechanisms ◽  
The Brain

Abstract Spatiotemporally ordered production of cells is essential for brain development. Normally, most undifferentiated neural progenitor cells (NPCs) face the apical (ventricular) surface of embryonic brain walls. Pathological detachment of NPCs from the apical surface and their invasion of outer neuronal territories, i.e., formation of NPC heterotopias, can disrupt the overall structure of the brain. Although NPC heterotopias have previously been observed in a variety of experimental contexts, the underlying mechanisms remain largely unknown. Yes-associated protein 1 (Yap1) and the TEA domain (Tead) proteins, which act downstream of Hippo signaling, enhance the stem-like characteristics of NPCs. Elevated expression of Yap1 or Tead in the neural tube (future spinal cord) induces massive NPC heterotopias, but Yap/Tead-induced expansion of NPCs in the developing brain has not been previously reported to produce NPC heterotopias. To determine whether NPC heterotopias occur in a regionally characteristic manner, we introduced the Yap1-S112A or Tead-VP16 into NPCs of the telencephalon and diencephalon, two neighboring but distinct forebrain regions, of embryonic day 10 mice by in utero electroporation, and compared NPC heterotopia formation. Although NPCs in both regions exhibited enhanced stem-like behaviors, heterotopias were larger and more frequent in the diencephalon than in the telencephalon. This result, the first example of Yap/Tead-induced NPC heterotopia in the forebrain, reveals that Yap/Tead-induced NPC heterotopia is not specific to the neural tube, and also suggests that this phenomenon depends on regional factors such as the three-dimensional geometry and assembly of these cells.

scholarly journals Neural Stem Cells/Neuronal Precursor Cells and Postmitotic Neuroblasts in Constitutive Neurogenesis and After ,Traumatic Injury to the Mesencephalic Tegmentum of Juvenile Chum Salmon, Oncorhynchus keta

2020 ◽  
Vol 10 (2) ◽  
pp. 65
Author(s):  
Pushchina ◽  
Kapustyanov ◽  
Varaksin
Keyword(s):  
Stem Cells ◽  
Neural Stem Cells ◽  
Progenitor Cells ◽  
Chum Salmon ◽  
Precursor Cells ◽  
Oncorhynchus Keta ◽  
Neuronal Precursor ◽  
Chum Salmon Oncorhynchus Keta ◽  
Neuronal Precursor Cells ◽  
Juvenile Chum Salmon

The proliferation of neural stem cells (NSCs)/neuronal precursor cells (NPCs) and the occurrence of postmitotic neuroblasts in the mesencephalic tegmentum of intact juvenile chum salmon, Oncorhynchus keta, and at 3 days after a tegmental injury, were studied by immunohistochemical labeling. BrdU+ constitutive progenitor cells located both in the periventricular matrix zone and in deeper subventricular and parenchymal layers of the brain are revealed in the tegmentum of juvenile chum salmon. As a result of traumatic damage to the tegmentum, the proliferation of resident progenitor cells of the neuroepithelial type increases. Nestin-positive and vimentin-positive NPCs and granules located in the periventricular and subventricular matrix zones, as well as in the parenchymal regions of the tegmentum, are revealed in the mesencephalic tegmentum of juvenile chum salmon, which indicates a high level of constructive metabolism and constitutive neurogenesis. The expression of vimentin and nestin in the extracellular space, as well as additionally in the NSCs and NPCs of the neuroepithelial phenotype, which do not express nestin in the control animals, is enhanced during the traumatic process. As a result of the proliferation of such cells in the post-traumatic period, local Nes+ and Vim+ NPCs clusters are formed and become involved in the reparative response. Along with the primary traumatic lesion, which coincides with the injury zone, additional Nes+ and Vim+ secondary lesions are observed to form in the adjacent subventricular and parenchymal zones of the tegmentum. In the lateral tegmentum, the number of doublecortin-positive cells is higher compared to that in the medial tegmentum, which determines the different intensities and rates of neuronal differentiation in the sensory and motor regions of the tegmentum, respectively. In periventricular regions remote from the injury, the expression of doublecortin in single cells and their groups significantly increases compared to that in the damage zone.

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