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2.
Neuromolecular Med ; 26(1): 17, 2024 Apr 29.
Artículo en Inglés | MEDLINE | ID: mdl-38684592

RESUMEN

Post-stroke neuroinflammation affects the damage and recovery of neurological functions. T cells including CD8+ T cells were present in the ipsilateral hemisphere in the subacute and late phases of ischemic stroke. However, the potential roles of CD8+ T cell subsets in the progression of neuroinflammation have not been characterized. In the current mouse transient middle cerebral artery occlusion model, we investigated the existence of CD8+ T cell subsets in the ipsilateral hemisphere in the subacute and late phases of stroke. We found that ipsilateral CD8+ T cells were present on post-stroke day 3 and increased on post-stroke day 30. The day-3 ipsilateral CD8+ T cells predominantly produced interferon-γ (IFN-γ), while the day-30 ipsilateral CD8+ T cells co-expressed IFN-γ and interleukin-17A (IL-17A). In addition, evaluation of cytokines and transcription factors of the day-30 ipsilateral CD8+ T cells revealed the presence of T cytotoxic 1 (Tc1), T cytotoxic 17 (Tc17), and T cytotoxic 17/1 (Tc17/1) cells. Furthermore, based on the expression of a series of chemokine/cytokine receptors, viable ipsilateral Tc1, Tc17, and Tc17.1 cells were identified and enriched from the day-30 ipsilateral CD8+ T cells, respectively. Co-culture of microglia with ipsilateral Tc1, Tc17, or Tc17.1 cells indicated that the three CD8+ T cell subsets up-regulated the expression of pro-inflammatory mediators by microglia, with Tc17.1 cells being the most potent cell in doing so. Collectively, this study sheds light on the contributions of Tc1, Tc17, and Tc17.1 cells to long-term neuroinflammation after ischemic stroke.


Asunto(s)
Infarto de la Arteria Cerebral Media , Interleucina-17 , Ratones Endogámicos C57BL , Microglía , Enfermedades Neuroinflamatorias , Linfocitos T Citotóxicos , Animales , Microglía/metabolismo , Ratones , Masculino , Infarto de la Arteria Cerebral Media/inmunología , Infarto de la Arteria Cerebral Media/patología , Linfocitos T Citotóxicos/inmunología , Enfermedades Neuroinflamatorias/etiología , Accidente Cerebrovascular Isquémico/inmunología , Interferón gamma/biosíntesis , Encéfalo , Células Th17/inmunología , Modelos Animales de Enfermedad , Linfocitos T CD8-positivos , Técnicas de Cocultivo , Células Cultivadas
3.
J Biol Chem ; 300(3): 105783, 2024 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-38395309

RESUMEN

Poly(ethylene terephthalate) (PET) is a major plastic polymer utilized in the single-use and textile industries. The discovery of PET-degrading enzymes (PETases) has led to an increased interest in the biological recycling of PET in addition to mechanical recycling. IsPETase from Ideonella sakaiensis is a candidate catalyst, but little is understood about its structure-function relationships with regards to PET degradation. To understand the effects of mutations on IsPETase productivity, we develop a directed evolution assay to identify mutations beneficial to PET film degradation at 30 °C. IsPETase also displays enzyme concentration-dependent inhibition effects, and surface crowding has been proposed as a causal phenomenon. Based on total internal reflectance fluorescence microscopy and adsorption experiments, IsPETase is likely experiencing crowded conditions on PET films. Molecular dynamics simulations of IsPETase variants reveal a decrease in active site flexibility in free enzymes and reduced probability of productive active site formation in substrate-bound enzymes under crowding. Hence, we develop a surface crowding model to analyze the biochemical effects of three hit mutations (T116P, S238N, S290P) that enhanced ambient temperature activity and/or thermostability. We find that T116P decreases susceptibility to crowding, resulting in higher PET degradation product accumulation despite no change in intrinsic catalytic rate. In conclusion, we show that a macromolecular crowding-based biochemical model can be used to analyze the effects of mutations on properties of PETases and that crowding behavior is a major property to be targeted for enzyme engineering for improved PET degradation.


Asunto(s)
Burkholderiales , Hidrolasas , Tereftalatos Polietilenos , Hidrolasas/química , Hidrolasas/genética , Hidrolasas/metabolismo , Tereftalatos Polietilenos/química , Tereftalatos Polietilenos/metabolismo , Reciclaje , Cinética , Burkholderiales/enzimología , Modelos Químicos
4.
Langmuir ; 38(26): 8114-8124, 2022 07 05.
Artículo en Inglés | MEDLINE | ID: mdl-35731984

RESUMEN

Many biological species combine the helical organization of cellulose or chitin microfibrils with broadband light absorption of black melanin to produce brilliant structural colors with metallic and glossy effects and other diverse functions. In this work, based on core-shell CNC@PDA chiral nanorods consisting of cellulose nanocrystals (CNCs) as the core and melanin-like polydopamine (PDA) as the shell that can form well-defined chiral liquid crystal phases, we report chiral photonic materials that closely mimic the unique coloration mechanisms and functionalities mastered by several biological species. The photonic films formed by such single CNC@PDA nanorods have brilliant iridescent structural colors originating from selective reflection of circularly polarized lights by the helical organization of CNC@PDAs across the films. Furthermore, the colors of such films have background-independent brightness, high visibility, and metallic effects that arise from the light absorption of the PDA component. Especially, the color ranges and metallic effects of the films can be conveniently tuned by varying the thickness of the PDA shell. In addition, the UV absorption and hygroscopic properties of PDA endow these CNC@PDA films with efficient broadband UV shielding and sensitive humidity-induced dynamic color changes. Due to the mussel-like superior adhesion of PDA, CNC@PDA-based photonic coatings can be formed conformably onto diverse kinds of substrates. A shiny eye shadow with viewing angle-dependent colorful patterns was used to demonstrate the potential applications. With combinations of multiple unique properties in one photonic material fabricated from a single building block, these CNC@PDA-based films are expected to have potential applications in cosmetics, UV protection, anticounterfeiting, chiral reflectors, etc.


Asunto(s)
Cosméticos , Nanotubos , Biomimética , Celulosa/química , Humedad , Melaninas/química
5.
Anal Methods ; 12(19): 2476-2483, 2020 05 21.
Artículo en Inglés | MEDLINE | ID: mdl-32930237

RESUMEN

Two fluorescent probes (L1 and L2) based on an imidazole unit were synthesized for the specific detection of ClO- and HSO3-. Density functional theory (DFT) calculations were used to assist in designing the probes. As predicted, L1 could be used to detect ClO- in real water samples and in living cells. It was shown to be a quenching probe. L2 could be used to monitor HSO3- in living cells and is an enhanced fluorescence probe. Further details of the fluorescence recognition mechanism were obtained via HRMS analysis. Moreover, both fluorescent probes showed relatively low detection limits (0.96 and 0.59 µM, respectively), and fast and highly selective fluorescence responses.

6.
Biomacromolecules ; 21(6): 2376-2390, 2020 06 08.
Artículo en Inglés | MEDLINE | ID: mdl-32364722

RESUMEN

The current work investigates how the nanoscale conformal coating layers of non-chiral polymeric materials can influence the chiral nematic liquid crystal (CLC) behaviors of the rodlike cellulose nanocrystals (CNCs), the bio-derived nanomaterials that have attracted significant attention. For this, we developed strategies to coat the CNC rods on the single-particle level with a homogeneous bioinspired polydopamine (PDA) layer, leading to well-defined core-shell CNC@PDA rods with various PDA coating thicknesses and excellent colloidal stability. Comprehensive investigation revealed that the CNC@PDA hybrid nanorods in concentrated suspensions form well-defined nematic liquid crystal phases with clear phase separation behavior that depend on the rod concentrations and ionic strengths, typical of charged rods. Most intriguingly, the nematic LC phases formed by the CNC@PDA rods with the PDA coating thickness achieved herein are indeed the perfect CLC phases, which form following the classic pathway of nucleation and coalesce of chiral tactoids and have colorful chiral fingerprints standing out from the dark suspensions. The pitches of the CLC phase increase sharply with increasing PDA coating thicknesses and are significantly larger than those of the pristine CNCs. Such observations can be attributed to the blurring effects of the PDA coating on the intrinsic surface chiral features of CNC of whatever origins that drive the formation of the CLC phases, resulting in weakening chiral interactions between CNC@PDA rods. Besides benefiting the understanding of the long-sought origin of the CLC phases of the pristine CNC, the current work demonstrates the possibility of controlling the CLC phase behaviors of CNC by tuning the thickness of the coating materials and also serves as the first example of directly transferring the unique chirality of CNC to other non-chiral materials.


Asunto(s)
Cristales Líquidos , Nanopartículas , Nanoestructuras , Celulosa , Suspensiones
7.
Arch Virol ; 164(7): 1805-1814, 2019 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-31087190

RESUMEN

The recombinant vaccinia virus VG9 and the STAT3 inhibitor Stattic were combined to kill cancer cells via both oncolytic activity and inhibition of STAT3 phosphorylation in cells. The combinatory anti-tumour activity of these compounds was superior to the activity of VG9 or Stattic alone in vivo. The inhibition of tumour growth occurred via increased apoptosis and autophagy pathways. Furthermore, the combinatory anti-tumour activity was more efficient than that of VG9 or Stattic alone on xenografts, especially in nude mice.


Asunto(s)
Antineoplásicos/farmacología , Proliferación Celular/efectos de los fármacos , Óxidos S-Cíclicos/farmacología , Neoplasias/terapia , Virus Oncolíticos/metabolismo , Factor de Transcripción STAT3/antagonistas & inhibidores , Virus Vaccinia/metabolismo , Animales , Apoptosis/efectos de los fármacos , Línea Celular Tumoral , Células HeLa , Humanos , Ratones , Ratones Endogámicos BALB C , Ratones Desnudos , Viroterapia Oncolítica/métodos , Fosforilación/efectos de los fármacos , Ensayos Antitumor por Modelo de Xenoinjerto
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