About: Caspase1/11 signaling affects muscle regeneration and recovery following ischemia, and can be modulated by chloroquine

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About: Caspase1/11 signaling affects muscle regeneration and recovery following ischemia, and can be modulated by chloroquine Goto Sponge NotDistinct Permalink

An Entity of Type : schema:ScholarlyArticle, within Data Space : wasabi.inria.fr associated with source document(s)

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type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	Caspase1/11 signaling affects muscle regeneration and recovery following ischemia, and can be modulated by chloroquine
Creator	Reynolds, Michael Ambrosio, Fabrisia Cui, Xiangdong Ferrari, Ricardo Liao, Hong Loughran, Patricia Pius, Abish Sachdev, Ulka Sahu, Amrita Scott, Melanie Shinde, Sunita Shiva, Sruti Sun, Ping
Source	Medline; PMC
abstract	BACKGROUND: We previously showed that the autophagy inhibitor chloroquine (CQ) increases inflammatory cleaved caspase-1 activity in myocytes, and that caspase-1/11 is protective in sterile liver injury. However, the role of caspase-1/11 in the recovery of muscle from ischemia caused by peripheral arterial disease is unknown. We hypothesized that caspase-1/11 mediates recovery in muscle via effects on autophagy and this is modulated by CQ. METHODS: C57Bl/6 J (WT) and caspase-1/11 double-knockout (KO) mice underwent femoral artery ligation (a model of hind-limb ischemia) with or without CQ (50 mg/kg IP every 2nd day). CQ effects on autophagosome formation, microtubule associated protein 1A/1B-light chain 3 (LC3), and caspase-1 expression was measured using electron microscopy and immunofluorescence. Laser Doppler perfusion imaging documented perfusion every 7 days. After 21 days, in situ physiologic testing in tibialis anterior muscle assessed peak force contraction, and myocyte size and fibrosis was also measured. Muscle satellite cell (MuSC) oxygen consumption rate (OCR) and extracellular acidification rate was measured. Caspase-1 and glycolytic enzyme expression was detected by Western blot. RESULTS: CQ increased autophagosomes, LC3 consolidation, total caspase-1 expression and cleaved caspase-1 in muscle. Perfusion, fibrosis, myofiber regeneration, muscle contraction, MuSC fusion, OCR, ECAR and glycolytic enzyme expression was variably affected by CQ depending on presence of caspase-1/11. CQ decreased perfusion recovery, fibrosis and myofiber size in WT but not caspase-1/11KO mice. CQ diminished peak force in whole muscle, and myocyte fusion in MuSC and these effects were exacerbated in caspase-1/11KO mice. CQ reductions in maximal respiration and ATP production were reduced in caspase-1/11KO mice. Caspase-1/11KO MuSC had significant increases in protein kinase isoforms and aldolase with decreased ECAR. CONCLUSION: Caspase-1/11 signaling affects the response to ischemia in muscle and effects are variably modulated by CQ. This may be critically important for disease treated with CQ and its derivatives, including novel viral diseases (e.g. COVID-19) that are expected to affect patients with comorbidities like cardiovascular disease.
has issue date	2020-07-08(xsd:dateTime)
bibo:doi	10.1186/s10020-020-00190-2
bibo:pmid	32641037
has license	cc-by
sha1sum (hex)	ed0cefb9af3e576c6972fa33590aebac4e45038e
schema:url	https://doi.org/10.1186/s10020-020-00190-2
resource representing a document's title	Caspase1/11 signaling affects muscle regeneration and recovery following ischemia, and can be modulated by chloroquine
has PubMed Central identifier	PMC7341481
has PubMed identifier	32641037
schema:publication	Mol Med
resource representing a document's body	covid:ed0cefb9af3e576c6972fa33590aebac4e45038e#body_text
is schema:about of	named entity 'satellite cell' named entity 'effects' named entity 'extracellular' covid:arg/ed0cefb9af3e576c6972fa33590aebac4e45038e named entity 'LC3' named entity '7 days' named entity 'situ' named entity 'inhibitor' named entity 'inflammatory' named entity 'C57Bl/6' named entity 'After' named entity 'autophagy' named entity 'ligation' named entity 'chloroquine' named entity 'myocyte' named entity 'Muscle' named entity 'myocytes' named entity 'perfusion' named entity 'autophagy' named entity 'caspase-1' named entity 'fibrosis' named entity 'ischemia' named entity 'chloroquine' named entity 'immunofluorescence' named entity 'femoral artery' named entity 'caspase-1' named entity 'muscle' named entity 'gene' named entity 'GAPDH' named entity 'CD56' named entity 'PBS' named entity 'treatment groups' named entity 'caspase-1' named entity 'non-ischemic' named entity 'ischemic tissue' named entity 'actin' named entity 'caspase-1' named entity 'PBS' named entity 'autophagy' named entity 'non-ischemic' named entity 'secondary antibody' named entity 'myofibers' named entity 'Autophagosomes' named entity 'ligation' named entity 'IHC' named entity 'autophagy' named entity 'mice' named entity 'muscle' named entity 'myofiber' named entity 'surgical procedures' named entity 'hepatocytes' named entity 'ischemia' named entity 'PBS' named entity 'caspase-1' named entity 'liquid nitrogen' named entity 'autophagy' named entity 'HCQ' named entity 'proximal and distal' named entity 'twitch' named entity 'cell plate' named entity 'atrophy' named entity 'Caspase-1' named entity 'myofibrils' named entity 'tetanic force' named entity 'IL18' named entity '21 days' named entity 'ATP production' named entity 'caspase-1' named entity 'muscle'

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