Publication: Sialic acid expression in human fetal skeletal muscle during limb early myogenesis
Authors
Marini, Mirca ; Sarchielli, Erica ; Zappoli Thyrion, Giorgia Donata ; Ambrosini, Stefano ; Sgambati, Eleonora
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Publisher
Universidad de Murcia. Departamento de BiologĂa Celular e HistologĂa
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DOI
DOI: 10.14670/HH-11-901
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info:eu-repo/semantics/article
Description
Abstract
Investigations on animal models
demonstrated that changes of sialic acid (SA)
expression, particularly the polymeric form, in the
skeletal muscle during embryonic and post-natal
development seem to be related to muscle differentiation
and functionality onset. The aim of this study was to
evaluate the monomeric and polymeric SA expression in
human skeletal muscle during early stages of fetal
development, when important morphofunctional events
occur. Specimens of fetal skeletal muscle from limb,
between 9 and 12 weeks of gestation (wg), were
obtained from 19 pregnant women. To investigate some
morphofunctional features occurring during this
development period, haematoxylin-eosin staining, tunel
assay and immunohistochemistry for connexin-43
(Cx43) and parvalbumin were performed. SA expression
and characterization was evaluated using lectin
histochemistry (MAA, SNA, PNA, SBA, DBA),
associated with enzymatic and chemical treatments.
Polysialic acid (PSA) expression was also evaluated
using immunohistochemistry. The results showed
apoptotic myotubes between 9 and 10.5 wg,
disappearing from 11 wg; Cx43 was more abundant in
myotubes/myoblasts between 9 and 9.5 wg, decreasing
and/or disappearing from 10 wg and parvalbumin was
present in myotubes between 10 and 10.5 wg. PSA was
revealed in myotubes/myoblasts from 9 to 10.5 wg; from
11 wg it was reduced or disappeared. Monomeric SA
appeared in myotubes/myoblasts from 10 wg, increasing
successively; acetylated SA was present from 11 wg.
These findings demonstrated that changes in expression
of various types of SA, occurring in human fetal skeletal
muscle during early development, seem to be related to
some morphofunctional aspects distinctive of this
organogenesis crucial period.
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Citation
Histology and Histopathology, Vol.32, nÂş11, (2017)
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