Pericytes are a distinct type of cells interacting with endothelial cells in blood vessels and contributing to endothelial barrier integrity. Furthermore, pericytes show mesenchymal stem cell properties. Muscle-derived pericytes can demonstrate both angiogenic and myogenic capabilities. It is well known that regenerative abilities and muscle stem cell potential decline during aging, leading to sarcopenia. Therefore, this study aimed to investigate the potential of pericytes in supporting muscle differentiation and angiogenesis in elderly individuals and in patients affected by Ullrich congenital muscular dystrophy or by Bethlem myopathy, two inherited conditions caused by mutations in collagen VI genes and sharing similarities with the progressive skeletal muscle changes observed during aging. The study characterized pericytes from different age groups and from individuals with collagen VI deficiency by mass spectrometry-based proteomic and bioinformatic analyses. The findings revealed that aged pericytes display metabolic changes comparable to those seen in aging skeletal muscle, as well as a decline in their stem potential, reduced protein synthesis, and alterations in focal adhesion and contractility, pointing to a decrease in their ability to form blood vessels. Strikingly, pericytes from young patients with collagen VI deficiency showed similar characteristics to aged pericytes, but were found to still handle oxidative stress effectively together with an enhanced angiogenic capacity.

Moriggi, M., Torretta, E., Cescon, M., Russo, L., Gregorio, I., Braghetta, P., et al. (2024). Characterization of Proteome Changes in Aged and Collagen VI-Deficient Human Pericyte Cultures. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 25(13) [10.3390/ijms25137118].

Characterization of Proteome Changes in Aged and Collagen VI-Deficient Human Pericyte Cultures

Cesare Gargioli;
2024-01-01

Abstract

Pericytes are a distinct type of cells interacting with endothelial cells in blood vessels and contributing to endothelial barrier integrity. Furthermore, pericytes show mesenchymal stem cell properties. Muscle-derived pericytes can demonstrate both angiogenic and myogenic capabilities. It is well known that regenerative abilities and muscle stem cell potential decline during aging, leading to sarcopenia. Therefore, this study aimed to investigate the potential of pericytes in supporting muscle differentiation and angiogenesis in elderly individuals and in patients affected by Ullrich congenital muscular dystrophy or by Bethlem myopathy, two inherited conditions caused by mutations in collagen VI genes and sharing similarities with the progressive skeletal muscle changes observed during aging. The study characterized pericytes from different age groups and from individuals with collagen VI deficiency by mass spectrometry-based proteomic and bioinformatic analyses. The findings revealed that aged pericytes display metabolic changes comparable to those seen in aging skeletal muscle, as well as a decline in their stem potential, reduced protein synthesis, and alterations in focal adhesion and contractility, pointing to a decrease in their ability to form blood vessels. Strikingly, pericytes from young patients with collagen VI deficiency showed similar characteristics to aged pericytes, but were found to still handle oxidative stress effectively together with an enhanced angiogenic capacity.
2024
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/13
Settore BIOS-10/A - Biologia cellulare e applicata
English
Con Impact Factor ISI
Bethlem myopathy
muscle aging
myogenic differentiation
pericyte
skeletal muscle
Ullrich congenital muscular dystrophy
Moriggi, M., Torretta, E., Cescon, M., Russo, L., Gregorio, I., Braghetta, P., et al. (2024). Characterization of Proteome Changes in Aged and Collagen VI-Deficient Human Pericyte Cultures. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 25(13) [10.3390/ijms25137118].
Moriggi, M; Torretta, E; Cescon, M; Russo, L; Gregorio, I; Braghetta, P; Sabatelli, P; Faldini, C; Merlini, L; Gargioli, C; Bonaldo, P; Gelfi, C; Capi...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/398403
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