2022
DOI: 10.1111/acel.13583
|View full text |Cite
|
Sign up to set email alerts
|

Coordination of mitochondrial and lysosomal homeostasis mitigates inflammation and muscle atrophy during aging

Abstract: This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
27
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 37 publications
(28 citation statements)
references
References 47 publications
1
27
0
Order By: Relevance
“…Interestingly, inflammation and mDAMPs synergistically contribute to sarcopenia [ 56 ]; for example, mDAMPs can activate the Toll-like receptor (TLR) pathway and trigger NF-κB signaling, thus increasing the expression of IL-6 and TNF-α [ 57 ]. Damaged mitochondria can activate the NLRP3 inflammasome, triggering the expression of the proteolytic cytokines IL-18 and IL-1β and enhancing inflammation, likely causing pyroptosis ( Figure 1 ) [ 58 ].…”
Section: Inflammation In Sarcopeniamentioning
confidence: 99%
“…Interestingly, inflammation and mDAMPs synergistically contribute to sarcopenia [ 56 ]; for example, mDAMPs can activate the Toll-like receptor (TLR) pathway and trigger NF-κB signaling, thus increasing the expression of IL-6 and TNF-α [ 57 ]. Damaged mitochondria can activate the NLRP3 inflammasome, triggering the expression of the proteolytic cytokines IL-18 and IL-1β and enhancing inflammation, likely causing pyroptosis ( Figure 1 ) [ 58 ].…”
Section: Inflammation In Sarcopeniamentioning
confidence: 99%
“…These compounds demonstrate a strong ability to activate anabolic pathways and to counteract age/disease-related changes involved in muscle degeneration, such as mitochondrial alterations and inflammatory processes [132]. In particular, several studies point to the role of EVOO in maintaining mitochondrial homeostasis through modulation of Sirt1 and PGC1-α expression (Figure 4), and this data appears extremely interesting, especially in light of the fact that accumulation of dysfunctional mitochondria is a major contributing factor to the development of sarcopenia [133][134][135]. Therefore, examining more closely the efficacy of EVOO phenols and studying their mechanisms of action in skeletal muscle models of aging both in vivo and in vitro are essential for designing new therapeutic approaches with the aim of treating sarcopenia.…”
Section: Discussionmentioning
confidence: 99%
“…Both sarcopenia and myosteatosis represent a loss of muscle function and quality. Inflammatory responses and oxidative stress are primary etiological factors in muscle wasting 39 . Inflammatory cytokines can disrupt the balance between muscle protein synthesis and degradation, leading to muscle wasting, 40 including chronic inflammation driven by interleukin‐1, interleukin‐6, and tumor necrosis factor‐alpha, which are associated with sarcopenia 41 .…”
Section: Discussionmentioning
confidence: 99%