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1.
Cell Physiol Biochem ; 37(2): 651-65, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26344791

RESUMO

BACKGROUND: Clinical results of regenerative treatments for osteoarthritis are becoming increasingly significant. However, several questions remain UNANSWERED concerning mesenchymal stem cell (MSC) adhesion and incorporation into cartilage. METHODS: To this end, peripheral blood (PB) MSCs were chondrogenically induced and/or stimulated with pulsed electromagnetic fields (PEMFs) for a brief period of time just sufficient to prime differentiation. In an organ culture study, PKH26 labelled MSCs were added at two different cell densities (0.5 x106 vs 1.0 x106). In total, 180 explants of six horses (30 per horse) were divided into five groups: no lesion (i), lesion alone (ii), lesion with naïve MSCs (iii), lesion with chondrogenically-induced MSCs (iv) and lesion with chondrogenically-induced and PEMF-stimulated MSCs (v). Half of the explants were mechanically loaded and compared with the unloaded equivalents. Within each circumstance, six explants were histologically evaluated at different time points (day 1, 5 and 14). RESULTS: COMP expression was selectively increased by chondrogenic induction (p = 0.0488). PEMF stimulation (1mT for 10 minutes) further augmented COL II expression over induced values (p = 0.0405). On the other hand, MSC markers remained constant over time after induction, indicating a largely predifferentiated state. In the unloaded group, MSCs adhered to the surface in 92.6% of the explants and penetrated into 40.7% of the lesions. On the other hand, physiological loading significantly reduced surface adherence (1.9%) and lesion filling (3.7%) in all the different conditions (p < 0.0001). Remarkably, homogenous cell distribution was characteristic for chondrogenic induced MSCs (+/- PEMFs), whereas clump formation occurred in 39% of uninduced MSC treated cartilage explants. Finally, unloaded explants seeded with a moderately low density of MSCs exhibited greater lesion filling (p = 0.0022) and surface adherence (p = 0.0161) than explants seeded with higher densities of MSCs. In all cases, the overall amount of lesion filling decreased from day 5 to 14 (p = 0.0156). CONCLUSION: The present study demonstrates that primed chondrogenic induction of MSCs at a lower cell density without loading results in significantly enhanced and homogenous MSC adhesion and incorporation into equine cartilage.


Assuntos
Condrogênese , Células-Tronco Mesenquimais/citologia , Técnicas de Cultura de Órgãos/métodos , Animais , Proteína de Matriz Oligomérica de Cartilagem/metabolismo , Adesão Celular , Contagem de Células , Diferenciação Celular , Células Cultivadas , Colágeno Tipo II/metabolismo , Campos Eletromagnéticos , Cavalos
2.
J Mater Chem B ; 2(4): 357-362, 2014 Jan 28.
Artigo em Inglês | MEDLINE | ID: mdl-32261380

RESUMO

Magnetic microrobots have potential use in biomedical applications such as minimally invasive surgery, targeted diagnosis and therapy. Inspired by nature, artificial bacterial flagella (ABFs) are a form of microrobot powered by magnetic helical propulsion. For the promise of ABFs to be realized, issues of biocompatibility must be addressed and the materials used in their fabrication should be carefully considered. In this work, we fabricate the helical bodies of ABFs from a commercially available biocompatible photoresist, ORMOCOMP, by subsequently coating them with Fe for magnetic actuation. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays show that Fe-coated ORMOCOMP layers do not undermine the cell viability during 72 hours of incubation compared to control substrates. Cells exhibit normal morphology on ABF arrays and show good lamellipodial and filopodial interactions with the ABF surfaces. The swimming performance of Fe-coated ABFs is characterized using a three-pair Helmholtz coil arrangement. ABFs exhibit a maximum forward speed of 48.9 µm s-1 under a field of 9 mT at a frequency of 72 Hz. In summary, our Fe-coated ABFs exhibit little cytotoxicity and have potential for in vivo applications, especially those involving difficult to access regions within the human body.

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