Fibroblast growth factors (FGFs) are believed to play a key role in tissue differentiation and maturation, Thus, the expression of the four members of the high-affinity tyrosine kinase FGF receptor family (FGFRs) and of the low-affinity heparan sulphate proteoglycan binding sites, syndecan-1 and perlecan, was studied in the human skeletal muscle during development. Northern blot analysis demonstrated a developmentally regulated expression of the mRNAs for FGFR-1, FGFR-3, FGFR-4, whereas only traces of FGFR-2 mRNA were found, Each receptor type had a different developmental pattern, suggesting an independent regulation, Signal for FGFR-3 was retained only in the adult muscle, Among the low-affinity FGF binding sites, perlecan was absent, whereas RNA transcript for syndecan-1 peaked at week 13 of gestation, after which a significant decrease was observed. Immunohistochemistry for FGFRs revealed that their localization changed with muscle maturation, At early embryonic stages, FGFR-3 and FGFR-4 had a scattered distribution in the tissue, and FGFR-1 was found on myotube and myofiber plasma membranes, At later stages, FGFR-1 positivity decreased and was found in a few areas of the muscle, FGFR-3 was concentrated in the nuclei of some, but not all, muscle fibers, and FGFR-4 maintained an association with plasma membrane, In adult tissue, weak positivity for FGFR-3 and FGFR-4 was observed in the connective tissue only, When immunocytochemistry was performed on human fetal myoblasts in culture, confocal microscope analysis revealed a nonhomogeneous cell membrane distribution of FGFRs. Taken together, the data strongly suggest that developmentally regulated expression and cell distribution of FGFRs play a role during muscle maturation. (C) 1998 Wiley-Liss, Inc.

Developmentally regulated expression and localization of fibroblast growth factor receptors in the human muscle

SOGOS, VALERIA;BALACI, LENUTA;ENNAS, MARIA GRAZIA;
1998-01-01

Abstract

Fibroblast growth factors (FGFs) are believed to play a key role in tissue differentiation and maturation, Thus, the expression of the four members of the high-affinity tyrosine kinase FGF receptor family (FGFRs) and of the low-affinity heparan sulphate proteoglycan binding sites, syndecan-1 and perlecan, was studied in the human skeletal muscle during development. Northern blot analysis demonstrated a developmentally regulated expression of the mRNAs for FGFR-1, FGFR-3, FGFR-4, whereas only traces of FGFR-2 mRNA were found, Each receptor type had a different developmental pattern, suggesting an independent regulation, Signal for FGFR-3 was retained only in the adult muscle, Among the low-affinity FGF binding sites, perlecan was absent, whereas RNA transcript for syndecan-1 peaked at week 13 of gestation, after which a significant decrease was observed. Immunohistochemistry for FGFRs revealed that their localization changed with muscle maturation, At early embryonic stages, FGFR-3 and FGFR-4 had a scattered distribution in the tissue, and FGFR-1 was found on myotube and myofiber plasma membranes, At later stages, FGFR-1 positivity decreased and was found in a few areas of the muscle, FGFR-3 was concentrated in the nuclei of some, but not all, muscle fibers, and FGFR-4 maintained an association with plasma membrane, In adult tissue, weak positivity for FGFR-3 and FGFR-4 was observed in the connective tissue only, When immunocytochemistry was performed on human fetal myoblasts in culture, confocal microscope analysis revealed a nonhomogeneous cell membrane distribution of FGFRs. Taken together, the data strongly suggest that developmentally regulated expression and cell distribution of FGFRs play a role during muscle maturation. (C) 1998 Wiley-Liss, Inc.
fibroblast growth factors; receptors;syndecan-1; muscle; muscle proteins;human fetus; development
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11584/95963
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