Results 81 to 90 of about 38,034 (262)

Extracellular Vesicles from the Myocyte Secretome Contribute In Vitro to Creating an Unfavourable Environment for Migrating Lung Carcinoma Cells

open access: yesBiology
Cancer progression in skeletal muscle (SkM) is very rare, and mechanisms remain unclear. This study assessed the potential of SkM (myocyte)-derived EVs (C2C12-EVs) as anti-cancer agents.
Dona Mannaperuma   +3 more
doaj   +1 more source

Dynamic Self‐Clickable Decellularized Matrix Hydrogels for Regulating Vascularity and Enhancing Muscle Regeneration

open access: yesAdvanced Science, EarlyView.
Dynamic decellularized hydrogels are prepared using bovine decellularized small intestine submucosa (SIS) norbornene (dSIS‐NB). Bovine dSIS contained significant amounts of disulfide‐rich fibrillin‐I, enabling ‘self‐clickable’ thiol‐norbornene gelation and spatiotemporal tuning of hydrogel physicochemical properties.
Van Thuy Duong   +4 more
wiley   +1 more source

Effects of Hoechst 33342 on C2C12 and PC12 cell differentiation [PDF]

open access: yesFEBS Letters, 2007
Accumulative evidence demonstrates that normal as well as cancer stem cells can be identified as a side population following Hoechst 33342 staining and flow cytometric analysis. This popular method is based on the ability of stem cells to efflux this fluorescent vital dye.
Adamski, Danièle   +5 more
openaire   +3 more sources

D151N/H155R double mutant rescues tubulation ability in C2C12 cells.

open access: yes, 2014
BIN N-BAR* WT and its mutants are fused to GFP and transiently transfected in C2C12 myoblasts. Cells are imaged by confocal fluorescence microscopy. Scale bar: 20 µm. Expression of BIN1 N-BAR* WT causes great membrane tubulation in C2C12 cells.
Zheng Shi (586636)   +2 more
core   +1 more source

Kinetin riboside but not Kinetin is toxic in C2C12 cells.

open access: yes, 2021
Kinetin but not Kinetin riboside supplement increased significantly A) fusion index and B) MCK activity, in C2C12 cells grown in GM with 15% FCS, in comparison to C2C12 myoblasts supplemented with DMSO only for 7 days. C) An MTT assay showed that Kinetin
Mark Isalan (26971)   +1 more
core   +1 more source

Myostatin promotes tenogenic differentiation of C2C12 myoblast cells through Smad3

open access: yesFEBS Open Bio, 2017
Myostatin, a member of the transforming growth factor‐β (TGF‐β) superfamily, is expressed in developing and adult skeletal muscle and negatively regulates skeletal muscle growth. Recently, myostatin has been found to be expressed in tendons and increases
Kazutaka Uemura   +7 more
doaj   +1 more source

Mechanosensitive Piezo1/Osteocalcin/Irisin Axis Protects Against Disuse‐Induced Muscle Atrophy

open access: yesAdvanced Science, EarlyView.
Mechanical unloading suppresses bone Piezo1 expression, which reduces circulating undercarboxylated osteocalcin (unOCN). unOCN reduction subsequently exacerbates IMM‐induced Fndc5/Irisin decrease and drives severe muscle atrophy. Bone Piezo1 activation or exogenous osteocalcin/Irisin ameliorate muscle atrophy, while muscle‐specific Gprc6a or Fndc5 ...
Zhaolu Wang   +5 more
wiley   +1 more source

Effect of mitochondrial fission inhibition on C2C12 differentiation

open access: yesData in Brief, 2016
The differentiation of skeletal muscle is commonly examined in cell culture using the C2C12 line of mouse skeletal myoblasts. This process shares many similarities with that which occurs during embryonic development, such as the transient activation of caspases.
Bloemberg, Darin, Quadrilatero, Joe
openaire   +3 more sources

Effects of thimerosal on proliferation of C2C12 myoblast cells.

open access: yes, 2013
C2C12 myoblast cells were treated with thimerosal (125, 250 and 500 nM) for 24, 48 or 72 h. A. C2C12 myoblast cell viability determined by WST-1. B. Cell cycle distribution of C2C12 myoblast cells analyzed by flow cytometry. C. The percentage of cells in
Hua-Zhang Liu (300078)   +6 more
core   +1 more source

Targeting PLD3 Reverses the Immunosuppressive Niche by Reprogramming Tumor‐Associated Macrophages and Potentiates Antitumor Immunity

open access: yesAdvanced Science, EarlyView.
PLD3 activates the lysosomal‐AKT‐NF‐κB axis to drive cellular senescence in macrophages, establishing an immunosuppressive TME by limiting the infiltration of cytotoxic T, NK, and NKT cells, which confers resistance to anti‐PD‐1 therapy. Abrine inhibits PLD3 expression, restoring antitumor immunity and synergizing with anti‐PD‐1 treatment.
Xingtu Qin   +11 more
wiley   +1 more source

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