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Batt, J.

Publications and source records attributed to Batt, J..

2 recordsLinked to original sources

Prostaglandin E2 is a Negative Regulator of Fibroadipogenic Progenitor Differentiation in Traumatically Denervated Skeletal Muscle

BackgroundPeripheral nerve trauma denervates skeletal muscle resulting in paralysis and atrophy that is reversible if timely reinnervation occurs, due to its regenerative capacity. If reinnervation is delayed muscles regenerative ability is exhausted and resident fibroadipogenic progenitors (FAPs) differentiate into adipocytes and fibroblasts that replace muscle with non-contractile fibrotic tissue and fat, resulting in physical disability. Prostaglandin E2 (PGE2) inhibits adipogenesis and fibrosis in other tissues. We determined whether PGE2 could inhibit fibro-fatty degradation of long-term denervated muscle. MethodsWe utilized the rat tibial nerve transection model, denervating the gastrocnemius and selected a 5 week post-denervation time point to represent short-term muscle denervation injury (reversible with reinnervation), and 12 weeks to represent sustained, irreversible injury. Gastrocnemius FAPs were isolated via FACS and grown in culture to assess endogenous PGE2 production and the proliferative and differentiation response to exogenous PGE2. We evaluated transcript and protein expression of PGE2 synthesizing enzyme PTGS2, PGE2 degrading enzyme 15-PGDH and markers of proliferation, adipogenesis and fibrogenesis using RT-qPCR, immunofluorescence and SDS-PAGE/Western blotting. Paracrine impact of FAPs produced PGE2 was assessed by treating C2C12 myoblasts with FAPs conditioned media. ResultsTranscript expression of PTGS2 was increased and 15-PGDH decreased (4.37{+/-}2.63 and -3.06{+/-}0.85 fold change respectively, p<0.05) in 5 week, but not 12 week denervated gastrocnemius, consistent with increased PGE2 production in 5 week denervated muscle. Similarly, PTGS2 transcript levels were significantly increased (2.58{+/-}0.33 fold change, p<0.05) and 15-PGDH decreased (-5.24{+/-}3.19 fold change, p<0.05) in FAPs isolated from 5 week, but not 12 week denervated muscle, demonstrating that FAPs are a source of PGE2 in short-term denervated muscle. 16,16-dimethyl PGE2 did not impact naive FAPs in vitro proliferation, but significantly inhibited their differentiation as demonstrated by 88.9%, 82.3% and 94.2% decreases in FAPs expression of adipogenic marker perilipin-1, fibrogenic marker -smooth muscle actin (-SMA) and lipid content respectively, mediated via PGE2 binding to the FAPs EP4 receptor. FAPs isolated from 12 week denervated muscle demonstrated increased adipogenesis and fibrogenesis vs. naive FAPs (perilipin-1 and -SMA 7.93{+/-}2.96 and 2.00{+/-}0.33 fold increase respectively, p<0.05) and remained fully susceptible to PGE2 inhibition of fibro-adipogenic differentiation. Conditioned media from FAPs derived from 5 week, but not 12 week, denervated gastrocnemius stimulated C2C12 myoblast proliferation which was prevented by EP4 blockade. ConclusionsPGE2 is identified as a novel negative regulator of FAPs differentiation in traumatically denervated muscle, suggesting the therapeutic potential of PGE2 to prevent fibro-fatty degradation of long-term denervated muscle awaiting reinnervation.

cell biology↗

Clinical risk factors of intensive care unit acquired weakness predicted by human muscle microtissue response to humoral factors

1.ICUAW is an acquired phenomenon in the critically ill patient that is characterized by severe muscle weakness and atrophy. It results from both myopathic and neuropathic injury and is associated with heightened patient morbidity and mortality. Critical illness survivors exhibit variable functional outcomes following ICUAW, ranging from full recovery to persistent weakness with a significant negative impact on quality of life. Despite clinical importance, the mechanistic understanding of ICUAW remains incomplete, in part due to a paucity of tractable, species-specific experimental models. Previous studies have suggested a potential causative role of bloodborne factors, though this remains a matter of debate. To address these technological and knowledge gaps, we leveraged a 3-D human skeletal muscle microtissue (hMMT) culture platform to investigate the ability of humoral factors to directly impact pathogenesis of the myopathic component of ICUAW; critical illness myopathy (CIM). Blood serum collected from ICU patients within 72 hours of ICU admission was used to treat hMMTs for 6 days starting at a time-point when the myotubes were multinucleated, striated, and capable of generating force. hMMTs treated with serum from patients that survived the ICU stay exhibited several hallmarks of CIM including; significant reductions in myotube diameter (atrophy) and striation density, alongside functional declines in calcium release, peak force, and force kinetics. The in vitro profiles of ICU serum treated hMMTs displayed significant associations with known ICUAW and CIM clinical risk factors (e.g. age, length of ICU stay) such that individual patient risk factors could be predicted from serum-induced hMMT responses. An evaluation of hMMT responses enabled delineation of ICU non-survivors from healthy control and ICU survivors. This study offers an enabling technology for studies of CIM biology in the context of human cells while also delivering compelling evidence that humoral factors directly influence ICU-associated skeletal muscle pathogenesis. Together, these advances may inform strategies for preventing or treating ICUAW.

bioengineering↗