c2c12 myoblasts
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2021 ◽  
Vol 22 (24) ◽  
pp. 13352
Author(s):  
Mingfa Ling ◽  
Lulu Quan ◽  
Xumin Lai ◽  
Limin Lang ◽  
Fan Li ◽  
...  

It has been demonstrated that vascular endothelial growth factor B (VEGFB) plays a vital role in regulating vascular biological function. However, the role of VEGFB in regulating skeletal muscle cell proliferation and differentiation remains unclear. Thus, this study aimed to investigate the effects of VEGFB on C2C12 myoblast proliferation and differentiation and to explore the underlying mechanism. For proliferation, VEGFB significantly promoted the proliferation of C2C12 myoblasts with the upregulating expression of cyclin D1 and PCNA. Meanwhile, VEGFB enhanced vascular endothelial growth factor receptor 1 (VEGFR1) expression and activated the PI3K/Akt signaling pathway in a VEGFR1-dependent manner. In addition, the knockdown of VEGFR1 and inhibition of PI3K/Akt totally abolished the promotion of C2C12 proliferation induced by VEGFB, suggesting that VEGFB promoted C2C12 myoblast proliferation through the VEGFR1-PI3K/Akt signaling pathway. Regarding differentiation, VEGFB significantly stimulated the differentiation of C2C12 myoblasts via VEGFR, with elevated expressions of MyoG and MyHC. Furthermore, the knockdown of VEGFR1 rather than NRP1 eliminated the VEGFB-stimulated C2C12 differentiation. Moreover, VEGFB activated the PI3K/Akt/mTOR signaling pathway in a VEGFR1-dependent manner. However, the inhibition of PI3K/Akt/mTOR blocked the promotion of C2C12 myoblasts differentiation induced by VEGFB, indicating the involvement of the PI3K/Akt pathway. To conclude, these findings showed that VEGFB promoted C2C12 myoblast proliferation and differentiation via the VEGFR1-PI3K/Akt signaling pathway, providing new insights into the regulation of skeletal muscle development.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Haiwen Li ◽  
Li Xu ◽  
Yandi Gao ◽  
Yuanbojiao Zuo ◽  
Zuocheng Yang ◽  
...  

Abstract Background Anoctamin 5 (ANO5) is a membrane protein belonging to the TMEM16/Anoctamin family and its deficiency leads to the development of limb girdle muscular dystrophy R12 (LGMDR12). However, little has been known about the interactome of ANO5 and its cellular functions. Results In this study, we exploited a proximal labeling approach to identify the interacting proteins of ANO5 in C2C12 myoblasts stably expressing ANO5 tagged with BioID2. Mass spectrometry identified 41 unique proteins including BVES and POPDC3 specifically from ANO5-BioID2 samples, but not from BioID2 fused with ANO6 or MG53. The interaction between ANO5 and BVES was further confirmed by co-immunoprecipitation (Co-IP), and the N-terminus of ANO5 mediated the interaction with the C-terminus of BVES. ANO5 and BVES were co-localized in muscle cells and enriched at the endoplasmic reticulum (ER) membrane. Genome editing-mediated ANO5 or BVES disruption significantly suppressed C2C12 myoblast differentiation with little impact on proliferation. Conclusions Taken together, these data suggest that BVES is a novel interacting protein of ANO5, involved in regulation of muscle differentiation.


2021 ◽  
Author(s):  
Haiwen Li ◽  
Li Xu ◽  
Yandi Gao ◽  
Yuanbojiao Zuo ◽  
Zuocheng Yang ◽  
...  

Abstract Background: Anoctamin 5 (ANO5) is a membrane protein belonging to the TMEM16/Anoctamin family and its deficiency leads to the development of limb girdle muscular dystrophy R12 (LGMDR12). However, little has been known about the interactome of ANO5 and its cellular functions. Results: In this study, we exploited a proximal labeling approach to identify the interacting proteins of ANO5 in C2C12 myoblasts stably expressing ANO5 tagged with BioID2. Mass spectrometry identified 41 unique proteins specifically from ANO5-BioID2 samples but not BioID2 fused with ANO6 or MG53, including BVES and POPDC3. The interaction between ANO5 and BVES was further confirmed by co-immunoprecipitation (Co-IP), and the N-terminus of ANO5 mediated the interaction with BVES through its C-terminus. ANO5 and BVES were co-localized in muscle cells and enriched at the endoplasmic reticulum (ER) membrane. Genome editing-mediated ANO5 or BVES disruption significantly suppressed C2C12 myoblast differentiation with little impact on proliferation. Conclusions:Taken together, these data suggest that BVES is a novel interacting protein of ANO5, involved in regulation of muscle differentiation.


PLoS ONE ◽  
2021 ◽  
Vol 16 (10) ◽  
pp. e0258419
Author(s):  
Michal Mielcarek ◽  
Mark Isalan

Kinetin or N6-furfuryladenine (K) belongs to a class of plant hormones called cytokinins, which are biologically active molecules modulating many aspects of plant growth and development. However, biological activities of cytokinins are not only limited to plants; their effects on animals have been widely reported in the literature. Here, we found that Kinetin is a potent small molecule that efficiently stimulates differentiation of C2C12 myoblasts into myotubes in vitro. The highest efficacy was achieved at 1μM and 10μM Kinetin concentrations, in both mitogen-poor and rich media. More importantly, Kinetin was able to strongly stimulate the MyoD-dependent conversion of fibroblasts into myotubes. Kinetin alone did not give rise to fibroblast conversion and required MyoD; this demonstrates that Kinetin augments the molecular repertoire of necessary key regulatory factors to facilitate MyoD-mediated myogenic differentiation. This novel Kinetin pro-myogenic function may be explained by its ability to alter intracellular calcium levels and by its potential to impact on Reactive Oxygen Species (ROS) signalling. Taken together, our findings unravel the effects of a new class of small molecules with potent pro-myogenic activities. This opens up new therapeutic avenues with potential for treating skeletal muscle diseases related to muscle aging and wasting.


Cells ◽  
2021 ◽  
Vol 10 (10) ◽  
pp. 2725
Author(s):  
Mai Thi Nguyen ◽  
Wan Lee

Skeletal myogenesis is required to maintain muscle mass and integrity, and impaired myogenesis is causally linked to the etiology of muscle wasting. Recently, it was shown that excessive uptake of saturated fatty acids (SFA) plays a significant role in the pathogenesis of muscle wasting. Although microRNA (miRNA) is implicated in the regulation of myogenesis, the molecular mechanism whereby SFA-induced miRNAs impair myogenic differentiation remains largely unknown. Here, we investigated the regulatory roles of miR-325-3p on CFL2 expression and myogenic differentiation in C2C12 myoblasts. PA impeded myogenic differentiation, concomitantly suppressed CFL2 and induced miR-325-3p. Dual-luciferase analysis revealed that miR-325-3p directly targets the 3′UTR of CFL2, thereby suppressing the expression of CFL2, a crucial factor for actin dynamics. Transfection with miR-325-3p mimic resulted in the accumulation of actin filaments (F-actin) and nuclear Yes-associated protein (YAP) in myoblasts and promoted myoblast proliferation and cell cycle progression. Consequently, miR-325-3p mimic significantly attenuated the expressions of myogenic factors and thereby impaired the myogenic differentiation of myoblasts. The roles of miR-325-3p on CFL2 expression, F-actin modulation, and myogenic differentiation suggest a novel miRNA-mediated regulatory mechanism of myogenesis and PA-inducible miR-325-3p may be a critical mediator between obesity and muscle wasting.


2021 ◽  
Vol 12 ◽  
Author(s):  
Ling Zhang ◽  
Jianguo Wang ◽  
Yu Tina Zhao ◽  
Patrycja Dubielecka ◽  
Gangjian Qin ◽  
...  

Background: p38 regulated/activated protein kinase (PRAK) plays a crucial role in modulating cell death and survival. However, the role of PRAK in the regulation of metabolic stress remains unclear. We examined the effects of PRAK on cell survival and mitochondrial function in C2C12 myoblasts in response to high glucose stresses.Methods: PRAK of C2C12 myoblasts was knocked out by using CRISPR/Cas-9 genome editing technology. Both wild type and PRAK−/− C2C12 cells were exposed to high glucose at the concentration of 30 mmol/L to induce metabolic stress. The effect of irisin, an adipomyokine, on both wild type and PRAK−/− cells was determined to explore its relationship with RPAK. Cell viability, ATP product, glucose uptake, mitochondrial damage, and insulin signaling were assessed.Results: PRAK knockout decreased C2C12 viability in response to high glucose stress as evident by MTT assay in association with the reduction of ATP and glucose uptake. PRAK knockout enhanced apoptosis of C2C12 myoblasts in response to high glucose, consistent with an impairment in mitochondrial function, by decreasing mitochondrial membrane potential. PRAK knockout induced impairment of mitochondrial and cell damage were rescued by irisin. PRAK knockout caused decrease in phosphorylated PI3 kinase at Tyr 485, IRS-1 and AMPKα and but did not affect non-phosphorylated PI3 kinase, IRS-1 and AMPKα signaling. High glucose caused the further reduction of phosphorylated PI3 kinase, IRS-1 and AMPKα. Irisin treatment preserved phosphorylated PI3 kinase, IRS-1by rescuing PRAK in high glucose treatment.Conclusion: Our finding indicates a pivotal role of PRAK in preserving cellular survival, mitochondrial function, and high glucose stress.


Biomolecules ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 1454
Author(s):  
Jia Wang ◽  
Huayue Zhang ◽  
Ashish Kaul ◽  
Kejuan Li ◽  
Didik Priyandoko ◽  
...  

Withania somnifera (Ashwagandha) is used in Indian traditional medicine, Ayurveda, and is believed to have a variety of health-promoting effects. The molecular mechanisms and pathways underlying these effects have not yet been sufficiently explored. In this study, we investigated the effect of Ashwagandha extracts and their major withanolides (withaferin A and withanone) on muscle cell differentiation using C2C12 myoblasts. We found that withaferin A and withanone and Ashwagandha extracts possessing different ratios of these active ingredients have different effects on the differentiation of C2C12. Withanone and withanone-rich extracts caused stronger differentiation of myoblasts to myotubes, deaggregation of heat- and metal-stress-induced aggregated proteins, and activation of hypoxia and autophagy pathways. Of note, the Parkinson’s disease model of Drosophila that possess a neuromuscular disorder showed improvement in their flight and climbing activity, suggesting the potential of Ashwagandha withanolides for the management of muscle repair and activity.


Molecules ◽  
2021 ◽  
Vol 26 (18) ◽  
pp. 5685
Author(s):  
Kento Mori ◽  
Hongkai Sun ◽  
Kazuki Miura ◽  
Siro Simizu

DPY19L3 has been identified as a C-mannosyltransferase for thrombospondin type-1 repeat domain-containing proteins. In this study, we focused on the role of DPY19L3 in the myogenic differentiation of C2C12 mouse myoblast cells. We carried out DPY19L3 gene depletion using the CRISPR/Cas9 system. The result showed that these DPY19L3-knockout cells could not be induced for differentiation. Moreover, the phosphorylation levels of MEK/ERK and p70S6K were suppressed in the DPY19L3-knockout cells compared with that of parent cells, suggesting that the protein(s) that is(are) DPY19L3-mediated C-mannosylated and regulate(s) MEK/ERK or p70S6K signaling is(are) required for the differentiation.


2021 ◽  
Vol 18 (1) ◽  
Author(s):  
Shaoting Fu ◽  
Xiaojing Lin ◽  
Lijun Yin ◽  
Xiaohui Wang

Abstract Background Androgen receptor (AR) exerts important roles in exercise-induced alterations of muscle mass, in which the proliferation and differentiation of satellite cells or myoblasts are crucial. Our previous study in C2C12 myoblasts demonstrated that 15% (mimic appropriate exercise) and 20% (mimic excessive exercise) stretches promoted and inhibited the proliferation respectively; and AR played a crucial role in 15% stretch-induced pro-proliferation through IGF-1-modulated PI3K/Akt, p38 and ERK1/2 pathways, but AR’s role in stretches-modulated proliferation of general myoblasts, especially 20% stretch, remains unclear, and the mechanisms need to be further clarified. Methods Firstly, the discrepancy in proliferation and the above indicators between L6 (without AR) and C2C12 (with AR) myoblasts were compared under 15% or 20% stretch. Then the influences of transfection AR or exogenous IGF-1 treatment on proliferation and these indicators were detected in stretched L6 myoblasts. Results (1) Under un-stretched state, the proliferation of L6 was slower than C2C12 cells. Furthermore, AR knockdown in C2C12 myoblasts repressed, while AR overexpression in L6 myoblasts promoted the proliferation. (2) 15% stretch-induced increases in the proliferation and activities of p38 and ERK1/2 were lower in L6 than C2C12 cells; AR overexpression enhanced the proliferation of 15% stretched L6 cells accompanied with the increases of p38 and ERK1/2 activities. (3) 20% stretch-induced anti-proliferation and inhibition of p38 activity were severer in L6 than C2C12 myoblasts; AR overexpression reversed the anti-proliferation of 20% stretch and enhanced p38 activity in L6 myoblasts. (4) In stretched L6 myoblasts, AR overexpression increased IGF-1R level despite no detectable IGF-1; and recombinant IGF-1 increased the proliferation, the level of IGF-1R, and the activities of p38 and ERK1/2 in 15% stretched L6 myoblasts. Conclusions The study demonstrated AR's crucial roles in stretches-regulated proliferation of myoblasts, and increased AR fulfilled 15% stretch's pro-proliferation via activating IGF-1R- p38 and ERK1/2 pathways while decreased AR achieved 20% stretch's anti-proliferation via inhibiting IGF-1R- p38 pathway, which is useful to understand in depth the role and mechanisms of AR in appropriate exercise increasing while excessive exercise decreasing muscle mass.


2021 ◽  
Author(s):  
Jianhong Cheng ◽  
Shasha Hong ◽  
Lian Yang ◽  
Jianfeng Liu ◽  
Li Hong

Abstract Background: Macrophages are involved in the regeneration of skeletal muscle injury and the exosomes secreted by a variety of cells promote the regeneration of tissues after injury. However, the potential effect of exosomes secreted by polarized macrophages on the repair of skeletal muscle after injury remains unclear. This study explored the effect of exosomes derived from M1 macrophages (M1-Exo) on the repair of levator ani muscle in mice after Vaginal Dilation (VD) modeling and the viability of C2C12 myoblasts after mechanical injury.Methods: Differential ultracentrifugation was used to separate M1-Exo from 200 ng/mL lipopolysaccharide-induced polarization of M1 type macrophages culture medium. Nanoparticle tracking analysis, transmission electron microscopy, and western blotting of CD9 and Tsg101 proteins were employed to identify M1-Exo. In vivo experiment involving the vaginal balloon expansion method was used to simulate the trauma to the pelvic floor of the mouse during delivery. M1-Exo was injected into the levator ani muscle and its surroundings to detect the abdominal leak point pressure (ALPP) and the maximum bladder volume (MBV) of the VD mice at 3, 7, and 14 days. Then the levator ani muscle was taken for hematoxylin and eosin (H&E) staining to observe the muscle damage and repair. To evaluate the functional and anatomical recovery of M1-Exo on stress urinary incontinence (SUI) mice caused by VD model delivery trauma. Subsequently, an in vitro C2C12 myoblasts cyclic mechanical strain injury model was constructed to determine the best mechanical injury parameters. In the next step, through a series of in vitro functional tests, the effect of M1-Exo on the proliferation, senescence, and apoptosis of C2C12 myoblasts injured by cyclic mechanical strain was assessed. The effect of M1-Exo on the prevention and treatment of SUI caused by injury to the levator ani muscle after delivery was evaluated using animal experiments and cell-level studies.Results: Powerlab software test results showed that the injection of M1-Exo into the levator ani muscle of SUI mice and its surroundings can significantly increase the mouse's ALPP, and MBV. H&E staining results revealed that M1-Exo can prevent secondary necrosis of broken muscle fibers, reduce nuclear migration of muscle fibers, maintain the shape of the muscle bundles, and promote normal muscle regeneration. CCK-8 proliferation reagent, senescence-associated β-galactosidase (SA-β-Gal) staining, and flow cytometry (PE/7-AAD staining) were used to determine the best in vitro simulation of the C212 myoblasts. The best damage parameters of the C2C12 myoblast injury model occurred at 5333 μ strain for a duration of 8 hours at 1 Hz. Subsequently, the test results of the CCK-8 proliferation reagent and EdU cell proliferation reagent suggested that M1-Exo promoted the proliferation of C2C12 myoblasts subjected to mechanically induced damage. SA-β-Gal staining results indicated that M1-Exo delayed the senescence of C2C12 myoblasts subjected to mechanically induced injury. Hoechst 33258 staining reagent and flow cytometry (PE/7-AAD staining) revealed that M1-Exo inhibited mechanically induced apoptosis of the C2C12 myoblasts.Conclusions: Our experimental results established that M1-Exo helps in the functional and anatomical recovery of SUI mice caused by labor trauma. Furthermore, the findings imply that M1-Exo has a protective effect on C2C12 myoblasts after cyclic mechanical strain damage, promotes their proliferation, delays aging, and inhibits apoptosis.


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