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Title:
Human muscle satellite cells show age-related differential expression of S100B protein and RAGE | GeroScience
Description:
During aging, skeletal muscles show reduced mass and functional capacity largely due to loss of the regenerative ability of satellite cells (SCs), the quiescent stem cells located beneath the basal lamina surrounding each myofiber. While both the external environment and intrinsic properties of SCs appear to contribute to the age-related SC deficiency, the latter ones have been poorly investigated especially in humans. In the present work, we analyzed several parameters of SCs derived from biopsies of vastus lateralis muscle from healthy non-trained young (28.7â±â5.9 years; nâ=â10) and aged (77.3â±â6.4 years; nâ=â11) people. Compared with young SCs, aged SCs showed impaired differentiation when cultured in differentiation medium, and exhibited the following: (1) reduced proliferation; (2) higher expression levels of S100B, a negative regulator of myoblast differentiation; (3) undetectable levels in growth medium of full-length RAGE (receptor for advanced glycation end products), a multiligand receptor of the immunoglobulin superfamily, the engagement of which enhances myoblast differentiation; and (4) lower expression levels of the transcription factors, MyoD and Pax7. Also, either overexpression of full-length RAGE or knockdown of S100B in aged SCs resulted in enhanced differentiation, while overexpression of either a non-transducing mutant of RAGE (RAGEÎcyto) or S100B in young SCs resulted in reduced differentiation compared with controls. Moreover, while aged SCs maintained the ability to respond to mitogenic factors (e.g., bFGF and S100B), they were no longer able to secrete these factors, unlike young SCs. These data support a role for intrinsic factors, besides the extracellular environment in the defective SC function in aged skeletal muscles.
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Keywords {đ}
article, google, scholar, pubmed, cas, muscle, cell, cells, satellite, aging, skeletal, donato, rage, differentiation, sorci, biol, stem, human, riuzzi, scs, young, physiol, mol, myogenic, content, expression, myoblast, receptor, factor, beccafico, growth, products, access, privacy, cookies, agerelated, protein, puglielli, fulle, reduced, functional, aged, proliferation, levels, factors, sci, exp, myoblasts, data, publish,
Topics {âïž}
month download article/chapter rosa mancinelli & stefania fulle age-related sc deficiency satellite-cell pool size human satellite cells muscle satellite cells article age aims igf1/pi3k/akt pathways cell-mediated gene therapy nfâÎșb-dependent inhibition human endothelial cells satellite cells fail stefania fulle full article pdf age-dependent imbalance myod-/- satellite cells stem cells aging skeletal muscle vastus lateralis muscle age-related calcium-regulated proteins s100a1 inhibits myoblast differentiation glycogenosis type ii age-dependent effects myogenic progenitor cells rhabdomyosarcoma cells results privacy choices/manage cookies enhances myoblast differentiation higher expression levels lower expression levels satellite cell numbers satellite cell content acute muscle injury aged skeletal muscles author information authors stem cell growth factor-1 signalling satellite cells tumour necrosis factor myoblast cell lines nfâÎșb signaling muscle differentiation nerve growth factor muscle healthy aging skeletal muscle reduced differentiation compared ph-regulated effects nfâkappab require van hinsbergh vw van loon lj
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- Zammit PS (2008) All muscle satellite cells are equal, but are some more equal than others?
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headline:Human muscle satellite cells show age-related differential expression of S100B protein and RAGE
description:During aging, skeletal muscles show reduced mass and functional capacity largely due to loss of the regenerative ability of satellite cells (SCs), the quiescent stem cells located beneath the basal lamina surrounding each myofiber. While both the external environment and intrinsic properties of SCs appear to contribute to the age-related SC deficiency, the latter ones have been poorly investigated especially in humans. In the present work, we analyzed several parameters of SCs derived from biopsies of vastus lateralis muscle from healthy non-trained young (28.7â±â5.9 years; nâ=â10) and aged (77.3â±â6.4 years; nâ=â11) people. Compared with young SCs, aged SCs showed impaired differentiation when cultured in differentiation medium, and exhibited the following: (1) reduced proliferation; (2) higher expression levels of S100B, a negative regulator of myoblast differentiation; (3) undetectable levels in growth medium of full-length RAGE (receptor for advanced glycation end products), a multiligand receptor of the immunoglobulin superfamily, the engagement of which enhances myoblast differentiation; and (4) lower expression levels of the transcription factors, MyoD and Pax7. Also, either overexpression of full-length RAGE or knockdown of S100B in aged SCs resulted in enhanced differentiation, while overexpression of either a non-transducing mutant of RAGE (RAGEÎcyto) or S100B in young SCs resulted in reduced differentiation compared with controls. Moreover, while aged SCs maintained the ability to respond to mitogenic factors (e.g., bFGF and S100B), they were no longer able to secrete these factors, unlike young SCs. These data support a role for intrinsic factors, besides the extracellular environment in the defective SC function in aged skeletal muscles.
datePublished:2010-12-08T00:00:00Z
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Muscle satellite cells
Aging
Proliferation
Differentiation
S100B
RAGE
Cell Biology
Geriatrics/Gerontology
Molecular Medicine
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headline:Human muscle satellite cells show age-related differential expression of S100B protein and RAGE
description:During aging, skeletal muscles show reduced mass and functional capacity largely due to loss of the regenerative ability of satellite cells (SCs), the quiescent stem cells located beneath the basal lamina surrounding each myofiber. While both the external environment and intrinsic properties of SCs appear to contribute to the age-related SC deficiency, the latter ones have been poorly investigated especially in humans. In the present work, we analyzed several parameters of SCs derived from biopsies of vastus lateralis muscle from healthy non-trained young (28.7â±â5.9 years; nâ=â10) and aged (77.3â±â6.4 years; nâ=â11) people. Compared with young SCs, aged SCs showed impaired differentiation when cultured in differentiation medium, and exhibited the following: (1) reduced proliferation; (2) higher expression levels of S100B, a negative regulator of myoblast differentiation; (3) undetectable levels in growth medium of full-length RAGE (receptor for advanced glycation end products), a multiligand receptor of the immunoglobulin superfamily, the engagement of which enhances myoblast differentiation; and (4) lower expression levels of the transcription factors, MyoD and Pax7. Also, either overexpression of full-length RAGE or knockdown of S100B in aged SCs resulted in enhanced differentiation, while overexpression of either a non-transducing mutant of RAGE (RAGEÎcyto) or S100B in young SCs resulted in reduced differentiation compared with controls. Moreover, while aged SCs maintained the ability to respond to mitogenic factors (e.g., bFGF and S100B), they were no longer able to secrete these factors, unlike young SCs. These data support a role for intrinsic factors, besides the extracellular environment in the defective SC function in aged skeletal muscles.
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Aging
Proliferation
Differentiation
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RAGE
Cell Biology
Geriatrics/Gerontology
Molecular Medicine
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