scholarly journals Development of the Arterial Supply of the Spinal Cord Tissue Based on Radioanatomical and Histological Studies in Cattle

Author(s):  
Armin Thron ◽  
Peter Stoeter ◽  
Jasmin Schiessl ◽  
Andreas Prescher

Abstract Purpose Angiographic techniques have gained increasing importance in suspected vascular disease of the spinal cord. This demands an advanced understanding of spinal cord blood vessel anatomy and its embryologically founded broad spectrum of variations. The aim of this study was to improve knowledge on contentious issues concerning the development of spinal cord arterial supply in higher mammals and to offer visual information of high didactic value. Methods The prenatal development was examined in cattle, using multiplanar high-resolution microangiography of injected specimens and microscopic sections. The gestational ages of the 15 specimens were between the late embryonic and the early fetal period (5–11 weeks). Microangiography of the human spinal cord from an earlier published study were used to envisage an adult arterial vascularization pattern in higher mammals. Results Establishment of the unpaired anterior spinal artery (ASA) goes through two procedures of reconfiguration until achieving its final design. Regression of the primarily established anteromedian tract is observed in cattle fetuses of 9–10 weeks. Return to the ontogenetic disposition of bilateral symmetry and a burst of vascularization from all parts of the spinal meninges follow and include the anterior median fissure as a preferred vascular pathway. Large sulcal/central arteries longitudinally anastomosing between each other emerge on both sides of the midline. The embryological pattern of exclusive peripheral medullary supply must have been converted into a combined system of predominant central (centrifugal) supply of the enlargements before a final unpaired ASA can be reconstructed. Conclusion Previous investigators focused on the early embryonic development of spinal cord arteries and missed the profound remodeling of the vascular architecture in the early fetal period.

2016 ◽  
Vol 163 ◽  
pp. 177-184 ◽  
Author(s):  
Shuang Wang ◽  
Zhuowen Liang ◽  
Yuzhe Gong ◽  
Yaning Yin ◽  
Kaige Wang ◽  
...  

2020 ◽  
Vol 21 (24) ◽  
pp. 9356
Author(s):  
Marija Jurić ◽  
Julia Zeitler ◽  
Katarina Vukojević ◽  
Ivana Bočina ◽  
Maximilian Grobe ◽  
...  

Direct intercellular communication via gap junctions has an important role in the development of the nervous system, ranging from cell migration and neuronal differentiation to the formation of neuronal activity patterns. This study characterized and compared the specific spatio-temporal expression patterns of connexins (Cxs) 37, 43 and 45 during early human developmental stages (since the 5th until the 10th developmental week) in the spinal cord (SC) and dorsal root ganglia (DRG) using double immunofluorescence and transmission electron microscopy. We found the expression of all three investigated Cxs during early human development in all the areas of interest, in the SC, DRG, developing paravertebral ganglia of the sympathetic trunk, notochord and all three meningeal layers, with predominant expression of Cx37. Comparing the expression of different Cxs between distinct developmental periods, we did not find significant differences. Specific spatio-temporal pattern of Cxs expression might reflect their relevance in the development of all areas of interest via cellular interconnectivity and synchronization during the late embryonic and early fetal period of human development.


2013 ◽  
Vol 85 (18) ◽  
pp. 8741-8748 ◽  
Author(s):  
Jörg Hanrieder ◽  
Per Malmberg ◽  
Olle R. Lindberg ◽  
John S. Fletcher ◽  
Andrew G. Ewing

PLoS ONE ◽  
2012 ◽  
Vol 7 (9) ◽  
pp. e44184 ◽  
Author(s):  
Ernesto Picardi ◽  
Angela Gallo ◽  
Federica Galeano ◽  
Sara Tomaselli ◽  
Graziano Pesole

Author(s):  
Phan H. Truong ◽  
Peter J. Crouch ◽  
James B. W. Hilton ◽  
Catriona A. McLean ◽  
Roberto Cappai ◽  
...  

AbstractMotor neurone disease (MND) is a neurodegenerative disorder characterised by progressive destruction of motor neurons, muscle paralysis and death. The amyloid precursor protein (APP) is highly expressed in the central nervous system and has been shown to modulate disease outcomes in MND. APP is part of a gene family that includes the amyloid precursor-like protein 1 (APLP1) and 2 (APLP2) genes. In the present study, we investigated the role of APLP2 in MND through the examination of human spinal cord tissue and by crossing APLP2 knockout mice with the superoxide dismutase 1 (SOD1-G37R) transgenic mouse model of MND. We found the expression of APLP2 is elevated in the spinal cord from human cases of MND and that this feature of the human disease is reproduced in SOD1-G37R mice at the End-stage of their MND-like phenotype progression. APLP2 deletion in SOD1-G37R mice significantly delayed disease progression and increased the survival of female SOD1-G37R mice. Molecular and biochemical analysis showed female SOD1-G37R:APLP2−/− mice displayed improved innervation of the neuromuscular junction, ameliorated atrophy of muscle fibres with increased APP protein expression levels in the gastrocnemius muscle. These results indicate a sex-dependent role for APLP2 in mutant SOD1-mediated MND and further support the APP family as a potential target for further investigation into the cause and regulation of MND.


1986 ◽  
Vol 64 (3) ◽  
pp. 483-490 ◽  
Author(s):  
T. A. Rizvi ◽  
S. Wadhwa ◽  
R. D. Mehra ◽  
V. Bijlani

1982 ◽  
Vol 7 (4) ◽  
pp. 437-441 ◽  
Author(s):  
G. Rath ◽  
G. Gopinath ◽  
V. Bijlani

2000 ◽  
Vol 119 (2) ◽  
pp. 376-379 ◽  
Author(s):  
P. Biglioli ◽  
R. Spirito ◽  
M. Roberto ◽  
F. Grillo ◽  
A. Cannata ◽  
...  

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