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Latest publication 05/04/2023

Muscle Injuries Induce a Prostacyclin-PPARγ and PGC1a-FAO Spike That Boosts Rege

It is well-known that muscle regeneration declines with aging, and aged muscles undergo degenerative atrophy or sarcopenia. While exercise and...

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    [title] => Muscle Injuries Induce a Prostacyclin-PPARγ and PGC1a-FAO Spike That Boosts Rege
    [paragraph] => Muscle Injuries Induce a Prostacyclin-PPARγ and PGC1a-FAO Spike That Boosts Regeneration
    [content] => 

Authors
Luo L, Chua YB, Liu T, Liang K, Chua MJ, Ma W, Goh JW, Wang Y, Su J, Ho YS, Li CW, Liu KH, Teh BT, Yu K, Shyh-Chang N


Lab
University of Chinese Academy of Sciences, Beijing, P. R. China

Journal
Adv Sci (Weinh)

Abstract
It is well-known that muscle regeneration declines with aging, and aged muscles undergo degenerative atrophy or sarcopenia. While exercise and acute injury are both known to induce muscle regeneration, the molecular signals that help trigger muscle regeneration have remained unclear. Here, mass spectrometry imaging (MSI) is used to show that injured muscles induce a specific subset of prostanoids during regeneration, including PGG1, PGD2, and the prostacyclin PGI2. The spike in prostacyclin promotes skeletal muscle regeneration via myoblasts, and declines with aging. Mechanistically, the prostacyclin spike promotes a spike in PPARγ/PGC1a signaling, which induces a spike in fatty acid oxidation (FAO) to control myogenesis. LC-MS/MS and MSI further confirm that an early FAO spike is associated with normal regeneration, but muscle FAO became dysregulated during aging. Functional experiments demonstrate that the prostacyclin-PPARγ/PGC1a-FAO spike is necessary and sufficient to promote both young and aged muscle regeneration, and that prostacyclin can synergize with PPARγ/PGC1a-FAO signaling to restore aged muscles' regeneration and physical function. Given that the post-injury prostacyclin-PPARγ-FAO spike can be modulated pharmacologically and via post-exercise nutrition, this work has implications for how prostacyclin-PPARγ-FAO might be fine-tuned to promote regeneration and treat muscle diseases of aging.

BIOSEB Instruments Used
Grip strength test (BIO-GS4)

Keywords/Topics
General muscular system [meta_description] => [meta_keywords] => https://onlinelibrary.wiley.com/doi/pdf/10.1002/advs.202301519 [meta_title] => [link_rewrite] => muscle-injuries-induce-a-prostacyclin-ppar-and-pgc1a-fao-spike-that-boosts-regeneration [actif_langue] => 1 [read] => 849 [count_comments] => 0 [id] => 1875 [categories] => Array ( [63] => Array ( [id_prestablog_categorie] => 63 [title] => General muscular system [link_rewrite] => General-muscular-system ) [2] => Array ( [id_prestablog_categorie] => 2 [title] => Publications [link_rewrite] => publications ) ) [authors] => [paragraph_crop] => Muscle Injuries Induce a Prostacyclin-PPARγ and PGC1a-FAO Spike That Boosts Regeneration [link_for_unique] => 1 [products_liaison] => Array ( [48] => Array ( [name] => Grip strength test [description_short] =>

An easy way to objectively quantify the muscular strength of mice and rats, and to assess the effect of drugs, toxins, muscular (i.e. myopathy) and neurodegenerative diseases on muscular degeneration. It is widely used in conjunction with the ROTAROD motor coordination test: a normally coordinated rodent will show a decreased latency to fall off the rotating rod if its muscular strength is low. The Grip Strength Test is a must for your research on activity, motor control & coordination, and is particularly well suited for studies on Parkinson's & Huntington's disease.

New features GS4 - 2023: Color display with permanent backlight screen for easier reading, reset by footswitch, Improved battery time, Larger data memory of 500 values, Animal counter, USB port (charging/data transfer)

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