| Autor: |
Marini M; Department of Experimental and Clinical Medicine, Section of Anatomy and Histology, Careggi Hospital, University of Florence, Florence, Italy., Sarchielli E; Department of Experimental and Clinical Medicine, Section of Anatomy and Histology, Careggi Hospital, University of Florence, Florence, Italy., Zappoli Thyrion GD; Department of Surgery and Translational Medicine, Careggi Hospital, University of Florence, Florence, Italy., Ambrosini S; Department of Experimental and Clinical Medicine, Section of Anatomy and Histology, Careggi Hospital, University of Florence, Florence, Italy., Sgambati E; Department of Biosciences and Territory, University of Molise, Pesche (Isernia), Italy. eleonora.sgambati@unimol.it. |
| Jazyk: |
angličtina |
| Zdroj: |
Histology and histopathology [Histol Histopathol] 2017 Nov; Vol. 32 (11), pp. 1207-1221. Date of Electronic Publication: 2017 May 09. |
| DOI: |
10.14670/HH-11-901 |
| Abstrakt: |
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. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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