2020
DOI: 10.1016/j.actbio.2020.07.028
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Fibrinogen and magnesium combination biomaterials modulate macrophage phenotype, NF-kB signaling and crosstalk with mesenchymal stem/stromal cells

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Cited by 50 publications
(26 citation statements)
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“…After the scaffold material was implanted into the tissue, the phagocytosis of macrophages plays an important role in controlling inflammatory response ( Bessa-Gonçalves et al, 2020 ; Mahon et al, 2020 ; Yang et al, 2020 ). Macrophages can phagocytize apoptotic cells and eliminate pathogenic microorganisms, which is more conducive to the implantation of scaffold materials.…”
Section: Effects Of Hydrogel Stiffness On Tissue Repairmentioning
confidence: 99%
“…After the scaffold material was implanted into the tissue, the phagocytosis of macrophages plays an important role in controlling inflammatory response ( Bessa-Gonçalves et al, 2020 ; Mahon et al, 2020 ; Yang et al, 2020 ). Macrophages can phagocytize apoptotic cells and eliminate pathogenic microorganisms, which is more conducive to the implantation of scaffold materials.…”
Section: Effects Of Hydrogel Stiffness On Tissue Repairmentioning
confidence: 99%
“…Reducing the host responses through modulating macrophage polarization has been the focus of many recent studies. 18 , 21 24 In addition, the monocyte-macrophage cell lineage is known as a key player in bone regeneration and acute inflammatory response. This is largely owing to their high plasticity in response to environmental signals and their multiple roles in bone homeostasis.…”
Section: Introductionmentioning
confidence: 99%
“…Our results demonstrated that both uExo and dExo had ROS-scavenging activities and significantly reduced the oxidative stress in rSCs. Several studies have reported that MSC-derived exosomes combat oxidative stress-induced damage through adaptive regulation of the nuclear factor erythroid 2-related factor 2 (Nrf2) defense system [ 59 , 90 , 91 ]. Both dExo and uExo significantly improved the ROS defense capacity compared to control group.…”
Section: Discussionmentioning
confidence: 99%
“…Monocytes isolated from peripheral blood mononuclear cells from anonymous human blood samples and were provided by the Elutriation Core Facility at the University of Nebraska Medical Center. Differentiation of monocytes into Mɸ and M1 macrophage was performed following a protocol modified from previous studies [ 59 , 60 ]. Briefly, 5 × 10 5 monocytes were seeded on sterile glass coverslips in 24-well plates and then cultured for 6 days in RPMI 1640 medium (Gibco) containing 10% FBS, 1% P/S, and 50 ng/mL of recombinant granulocyte macrophage colony-stimulating factor (GM-CSF, PeproTech).…”
Section: Methodsmentioning
confidence: 99%