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1.
ACS Nano ; 18(24): 15815-15830, 2024 Jun 18.
Artigo em Inglês | MEDLINE | ID: mdl-38833572

RESUMO

Amyloid-like fibrils are garnering keen interest in biotechnology as supramolecular nanofunctional units to be used as biomimetic platforms to control cell behavior. Recent insights into fibril functionality have highlighted their importance in tissue structure, mechanical properties, and improved cell adhesion, emphasizing the need for scalable and high-kinetics fibril synthesis. In this study, we present the instantaneous and bulk formation of amyloid-like nanofibrils from human platelet lysate (PL) using the ionic liquid cholinium tosylate as a fibrillating agent. The instant fibrillation of PL proteins upon supramolecular protein-ionic liquid interactions was confirmed from the protein conformational transition toward cross-ß-sheet-rich structures. These nanofibrils were utilized as building blocks for the formation of thin and flexible free-standing membranes via solvent casting to support cell self-aggregation. These PL-derived fibril membranes reveal a nanotopographically rough surface and high stability over 14 days under cell culture conditions. The culture of mesenchymal stem cells or tumor cells on the top of the membrane demonstrated that cells are able to adhere and self-organize in a three-dimensional (3D) spheroid-like microtissue while tightly folding the fibril membrane. Results suggest that nanofibril membrane incorporation in cell aggregates can improve cell viability and metabolic activity, recreating native tissues' organization. Altogether, these PL-derived nanofibril membranes are suitable bioactive platforms to generate 3D cell-guided microtissues, which can be explored as bottom-up strategies to faithfully emulate native tissues in a fully human microenvironment.


Assuntos
Plaquetas , Nanofibras , Humanos , Plaquetas/metabolismo , Plaquetas/química , Nanofibras/química , Células-Tronco Mesenquimais/citologia , Células-Tronco Mesenquimais/metabolismo , Agregação Celular/efeitos dos fármacos , Adesão Celular/efeitos dos fármacos , Amiloide/química , Amiloide/metabolismo , Membranas Artificiais
2.
Ann Biomed Eng ; 2024 May 25.
Artigo em Inglês | MEDLINE | ID: mdl-38796670

RESUMO

Biomimetic tumor microenvironment models bridge the gap between in vitro and in vivo systems and serve as a useful way to address the modeling challenge of how to recreate the cell and system complexity associated with real tissues. Our laboratory has developed an ex vivo rat mesentery culture model, which allows for simultaneous investigation of blood and lymphatic microvascular network remodeling in an intact tissue environment. Given that angiogenesis and lymphangiogenesis are key contributors to the progression of cancer, the objective of this study was to combine tissue and tumor spheroid culture methods to establish a novel ex vivo tumor spheroid-tissue model by verifying its use for evaluating the effects of cancer cell behavior on the local microvascular environment. H1299 or A549 tumor spheroids were formed via hanging drop culture and seeded onto rat mesenteric tissues harvested from adult male Wistar rats. Tissues with transplanted spheroids were cultured in serum-free media for 3 to 5 days. PECAM, NG2, CD11b, and αSMA labeling identified endothelial cells, pericytes, immune cells, and smooth muscle cells, respectively. Time-lapse imaging confirmed cancer cell type specific migration. In addition to increasing PECAM positive capillary sprouting and LYVE-1 positive endothelial cell extensions indicative of lymphangiogenesis, tumor spheroid presence induced the formation of lymphatic/blood vessel connections and the formation of hybrid, mosaic vessels that were characterized by discontinuous LYVE-1 labeling. The results support the application of a novel tumor spheroid microenvironment model for investigating cancer cell-microvascular interactions.

3.
Artigo em Inglês | MEDLINE | ID: mdl-38546538

RESUMO

Biomaterial-mediated bone tissue engineering (BTE) offers an alternative, interesting approach for the restoration of damaged bone tissues in postsurgery osteosarcoma treatment. This study focused on synthesizing innovative composite inks, integrating self-assembled silk fibroin (SF), tannic acids (TA), and electrospun bioactive glass nanofibers 70SiO2-25CaO-5P2O5 (BGNF). By synergistically combining the unique characteristics of these three components through self-assembly and microextrusion-based three-dimensional (3D) printing, our goal was to produce durable and versatile aerogel-based 3D composite scaffolds. These scaffolds were designed to exhibit hierarchical porosity along with antibacterial, antiosteosarcoma, and bone regeneration properties. Taking inspiration from mussel foot protein attachment chemistry involving the coordination of dihydroxyphenylalanine (DOPA) amino acids with ferric ions (Fe3+), we synthesized a tris-complex catecholate-iron self-assembled composite gel. This gel formation occurred through the coordination of oxidized SF (SFO) with TA and polydopamine-modified BGNF (BGNF-PDA). The dynamic nature of the coordination ligand-metal bonds within the self-assembled SFO matrix provided excellent shear-thinning properties, allowing the SFO-TA-BGNF complex gel to be extruded through a nozzle, facilitating 3D printing into scaffolds with outstanding shape fidelity. Moreover, the developed composite aerogels exhibited multifaceted features, including NIR-triggered photothermal antibacterial and in vitro photothermal antiosteosarcoma properties. In vitro studies showcased their excellent biocompatibility and osteogenic features as seeded cells successfully differentiated into osteoblasts, promoting bone regeneration in 21 days. Through comprehensive characterizations and biological validations, our antibacterial scaffold demonstrated promise as an exceptional platform for concurrent bone regeneration and bone cancer therapy, setting the stage for their potential clinical application.

4.
Adv Mater ; 35(41): e2304659, 2023 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-37354139

RESUMO

There is a demand to design microparticles holding surface topography while presenting inherent bioactive cues for applications in the biomedical and biotechnological fields. Using the pool of proteins present in human-derived platelet lysates (PLs), the production of protein-based microparticles via a simple and cost-effective method is reported, exploring the prone redox behavior of cysteine (Cy-SH) amino acid residues. The forced formation of new intermolecular disulfide bonds results in the precipitation of the proteins as spherical, pompom-like microparticles with adjustable sizes (15-50 µm in diameter) and surface topography consisting of grooves and ridges. These PL microparticles exhibit extraordinary cytocompatibility, allowing cell-guided microaggregates to form, while also working as injectable systems for cell support. Early studies also suggest that the surface topography provided by these PL microparticles can support osteogenic behavior. Consequently, these PL microparticles may find use to create live tissues via bottom-up procedures or injectable tissue-defect fillers, particularly for bone regeneration, with the prospect of working under xeno-free conditions.


Assuntos
Regeneração Óssea , Engenharia Tecidual , Humanos , Engenharia Tecidual/métodos , Osteogênese
5.
Acta Biomater ; 149: 167-178, 2022 09 01.
Artigo em Inglês | MEDLINE | ID: mdl-35811072

RESUMO

Recreating the biological complexity of living bone marrow (BM) in a single in vitro strategy has faced many challenges. Most bioengineered strategies propose the co-culture of BM cellular components entrapped in different matrices limiting their migration and self-organization capacity or in open scaffolds enabling their escaping. We propose a methodology for fabricating a "human bone marrow-in-a-liquefied-capsule" to overcome these challenges, embracing the most important BM components in a single platform. Since free dispersion of the cells within the BM is an essential feature to maintain their in vivo properties, this platform provides a liquefied environment for the encapsulated cells to move freely and self-organize. Inside liquefied capsules, an engineered endosteal niche (eEN) is co-cultured with human umbilical cord cells, including endothelial cells and hematopoietic stem and progenitor cells (HSPCs). Two different human-like BM niches were recreated under static and dynamic systems. Although the culture of the engineered BM capsules (eBMC) in these different environments did not change the structural and compositional features of the BM niches, the biophysical stimulation potentiated the cellular intercommunication and the biomolecules secretion, demonstrating an enhanced in vitro bio performance. Moreover, while the eBMC without HSPCs provided the secretion of hematopoietic supportive factors, the presence of these cells recapitulated more closely the biological complexity of the native BM niches. This functional eBMC approach is an innovative platform capable of investigating several components and interactions of BM niches and how they regulate BM homeostasis and hematopoiesis. STATEMENT OF SIGNIFICANCE: The recapitulation of the multifaceted bone marrow (BM) microenvironment under in vitro conditions has gained intensive recognition to understand the intrinsic complexity of the native BM. While conventional strategies do not recapitulate the BM osteovascular niches nor give the cellular components a free movement, we report for the first time the development of human bone marrow-in-a-liquefied-capsule to overcome such limitations. Our engineered BM capsules (eBMC) partially mimic the complex structure, composition, and spatial organization of the native osteovascular niches present in the BM. This strategy offers a platform with physiological relevance to exploit the niches' components/networks and how they regulate the hematopoiesis and the initiation/progression of various BM-related pathologies.


Assuntos
Medula Óssea , Nicho de Células-Tronco , Bioengenharia , Células da Medula Óssea , Células Endoteliais , Células-Tronco Hematopoéticas , Humanos
6.
J Mater Chem B ; 9(45): 9285-9294, 2021 11 24.
Artigo em Inglês | MEDLINE | ID: mdl-34709285

RESUMO

Raman spectroscopy coupled with confocal microscopy offers an alternative bioimaging technique overcoming limitations associated with sensitivity, tissue penetration and image resolution. Allied to the surface-enhanced Raman scattering (SERS) properties of gold nanoparticles (AuNP), we designed SERS nanoprobes with enhanced properties and straightforward application as bio-labelling agents for gliomas. The ensuing nanoprobes coated with simple sugar units (galactose or glucose) allowed assessing information about their intracellular localization (vesicular structures), with impressive sensitivity towards complex environments and proved the ability to overcome biological auto-fluorescence and high penetration in tissues. We validate the use of sugars as an all-in-one vector (Raman reporter, conferring high stability, biocompatibility and affinity to glioma cells) as imaging agents using an impressive technique.


Assuntos
Galactose/química , Glucose/química , Ouro/química , Nanopartículas Metálicas/química , Análise Espectral Raman/métodos , Galactose/metabolismo , Galectinas/genética , Galectinas/metabolismo , Glucose/metabolismo , Proteínas de Transporte de Monossacarídeos/genética , Proteínas de Transporte de Monossacarídeos/metabolismo
7.
Adv Healthc Mater ; 10(19): e2100782, 2021 10.
Artigo em Inglês | MEDLINE | ID: mdl-34216107

RESUMO

Platforms with liquid cores are extensively explored as cell delivery vehicles for cell-based therapies and tissue engineering. However, the recurrence of synthetic materials can impair its translation into the clinic. Inspired by the adhesive proteins secreted by mussels, liquefied capsule is developed using gelatin modified with hydroxypyridinones (Gel-HOPO), a catechol analogue with oxidant-resistant properties. The protein-based liquefied macrocapsule permitted the compartmentalization of living cells by an approachable and non-time-consuming methodology resorting to i) superhydrophobic surfaces as a processing platform of hydrogel beads, ii) gelation of gelatin at temperatures < 25 °C, iii) iron coordination of the hydroxypyridinone (HOPO) moieties at physiological pH, and iv) core liquefaction at 37 °C. With the design of a proteolytically degradable shell, the possibility of encapsulating human adipose-derived mesenchymal stem cells (hASC) with and without the presence of polycaprolactone microparticles (µPCL) is evaluated. Showing prevalence toward adhesion to the inner shell wall, hASC formed a monolayer evidencing the biocompatibility and adequate mechanical properties of these platforms for proliferation, diminishing the need for µPCL as a supporting substrate. This new protein-based liquefied platform can provide biofactories devices of both fundamental and practical importance for tissue engineering and regenerative medicine or in other biotechnology fields.


Assuntos
Células-Tronco Mesenquimais , Engenharia Tecidual , Cápsulas , Gelatina , Humanos , Hidrogéis
8.
Sci Rep ; 11(1): 9099, 2021 04 27.
Artigo em Inglês | MEDLINE | ID: mdl-33907277

RESUMO

The sustainable cellular delivery of the pleiotropic drug curcumin encounters drawbacks related to its fast autoxidation at the physiological pH, cytotoxicity of delivery vehicles and poor cellular uptake. A biomaterial compatible with curcumin and with the appropriate structure to allow the correct curcumin encapsulation considering its poor solubility in water, while maintaining its stability for a safe release was developed. In this work, the biomaterial developed started by the preparation of an oil-in-water nanoemulsion using with a cytocompatible copolymer (Pluronic F 127) coated with a positively charged protein (gelatin), designed as G-Cur-NE, to mitigate the cytotoxicity issue of curcumin. These G-Cur-NE showed excellent capacity to stabilize curcumin, to increase its bio-accessibility, while allowing to arrest its autoxidation during its successful application as an anticancer agent proved by the disintegration of MDA-MB-231 breast cancer cells as a proof of concept.


Assuntos
Antineoplásicos Fitogênicos/farmacologia , Neoplasias da Mama/tratamento farmacológico , Curcumina/farmacologia , Emulsões/química , Nanoestruturas/química , Animais , Antineoplásicos Fitogênicos/administração & dosagem , Antineoplásicos Fitogênicos/química , Linhagem Celular Tumoral , Curcumina/administração & dosagem , Curcumina/química , Portadores de Fármacos/administração & dosagem , Portadores de Fármacos/química , Sistemas de Liberação de Medicamentos , Estabilidade de Medicamentos , Emulsões/administração & dosagem , Feminino , Fibroblastos , Gelatina/química , Humanos , Camundongos , Nanoestruturas/administração & dosagem , Azeite de Oliva/química , Poloxâmero/química , Água/química
9.
Liberabit ; 21(1): 91-101, ene.-jun.2015. tab
Artigo em Português | LILACS, LIPECS | ID: lil-783465

RESUMO

O consumo de álcool entre universitários tem sido um problema determinante para as relações interpessoais e desenvolvimento acadêmico, mas também um problema que traz um prejuízo social, econômico e de saúde. Medidas tem surgido e sugerida a reavaliação de outras para identificar o fenômeno do consumo de álcool. Porém, o Alcohol Use Disorders Identification Test (AUDIT) ainda tem sido o instrumento mais utilizado em estudos no mundo, o qual tem se revelado consistente. O presente estudo tem como objetivo avaliar a consistência interna e fatorial do AUDIT em universitários em diferentes estados brasileiros. O AUDIT e dados sociodemográficos foram respondidos por 639 universitários dos dois sexos, acima de 18 anos, distribuídos em diferentes cursos superiores de instituições particulares e públicas em quatro estados no Brasil. Realizando distintos cálculos estatísticos, observaram-se indicadores psicométricos que revelaram confiabilidade na medida do AUDIT na amostra pesquisada. Este procedimento tanto garantiu a medida sobre a identificação do problema do consumo de álcool quanto observou-se que, independente do contexto educacional dos universitários, nos referidos estados brasileiros, todos os respondentes revelaram problemas com o consumo alcoólico...


The consumption of alcohol in college students has been a crucial problem for interpersonal relationships and academic development; but it is also a problem that means a social, economic and health damage. It has been emerged and suggested measures to be ratified to identify the phenomenon of alcohol consumption. However, the Alcohol Use Disorders Identification Test (AUDIT) is still the most used instrument in world studies, the same one that has remained constant. The present research aims to assess the internal and factorial consistency of the AUDIT in college students from different Brazilian States. A total of 639 college students of both sexes over 18 years old, distributed in different advanced courses of public and private institutions in four Brazilian States, responded the AUDIT and socio-demographic data. Performing different statistical calculations, psychometric indicators were observed which gave confidence to the AUDIT measurement in the investigated sample. This procedure guaranteed the measure regarding the identification of the alcohol consumption problem, as it also observed that independent of the educational context of college students in the concerned Brazilian States, all respondents revealed problems with alcohol consumption...


Assuntos
Humanos , Masculino , Adolescente , Adulto , Feminino , Adulto Jovem , Consumo de Álcool por Menores , Consumo de Álcool na Faculdade
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