Hypertrophic scarring is a common occurrence for severe burn victims leading to major functional, physiological, and aesthetic effects to the patients. Limiting the hypertrophic scarring of the patients alleviates the functional, physiological, and aesthetic effects. Silicone gels, over the past decade, have been widely used to remediate and limit hypertrophic scarring but the mechanism of action is yet to be determined. One explanation has been that hydration of the outermost area of the burn is induced by the silicone gel . However, non-silicone polymers which increase hydration could not mimic the effect. An alternative interpretation is that there may be silicone species that migrate from the silicone gel into the viable tissue to mediate reactions in the extra-cellular matrix that result in a decreased deposition of excessive amounts of collagen - a central feature of the hypertrophic scar. A novel and informative technique to study these species is MALDI-TOF/MS (Matrix Assisted Laser Desorption Ionisation-Time of Flight Mass Spectrometry) in conjunction with gel permeation chromatography. MALDI-TOF/MS, which has allowed the detection of intact molecular species that were not possible with more established mass spectrometric techniques. The mobile species that may migrate from polydimethylsiloxane medical gel sheeting into skin have been identified by MALDI-MS. The bulk gel contains predominantly cyclic oligomers with a mass distribution peaking at n = 19 (number of repeating siloxane units), but in an aqueous environment the species at the surface of the silicone medical gel are predominantly methyl/methylol-terminated linear siloxanes. By using a gelatine matrix as a model substrate, the distribution of silicon after application of the silicone gel for 16 weeks was determined by Energy-dispersive X-Ray mapping of the sectioned gelatine. The association of the linear and cyclic oligomers with proteins relevant in hypertrophic scarring are considered. The mobility of silicone species across stratum corneum was confirmed by Attenuated Total Reflectance Fourier Transform Infrared spectroscopy (ATR-FT/IR). This method confirms our hypothesis that not only are the low molecular weight silicone species mobile, but also that they do traverse the natural barrier, the stratum corneum, to levels that are detectable by ATR after a continuous application over approximately 11 days. Invitro studies of the effects of LMWS on primary line fibroblast cells indicate a response that down regulates the proliferation of fibroblast cells and protein production. Preliminary results indicate that a family of pendant functional LMWS are effective in down regulating hypertrophic-derived fibroblast primary cells. Studies on hypertrophic scar tissue treated with silicone medical gel indicate that LMWS permeate across the stratum corneum into viable scar tissue. In some areas, the LMWS tend to pool as detected by SEM/EDX elemental silicon analysis. These areas of LMWS pooling tend to be composed of highly disorganised collagen nodules.

Diss. (sammanfattning) Umeå : Univ., 2007. / Härtill 3 uppsatser.

Thesis (Ph.D.). / Written for the Division of Experimental Medicine, Dept. of Medicine. Title from title page of PDF (viewed 2008/07/23). Includes bibliographical references.

Diss. (sammanfattning) Umeå : Univ., 2008. / Härtill 3 uppsatser.

Thesis (Ph. D.)--University of Washington, 2007. / Vita. Includes bibliographical references (leaves 117-139).

Rupture of the anterior cruciate ligament (ACL) of the knee leads to chronic joint instability and reduced range of motion while the long term results are marred by a high prevalence of degenerative joint disease especially osteoarthritis. Bundles of collagen threads have been widely investigated for the repair of torn ACL, but are limited by insufficient tissue ingrowth to repopulate and completely regenerate these grafts. We have developed a novel in vitro method of characterizing fiber-based thread matrices by probing their ability to promote tissue ingrowth from a wound margin as a measure of their ability to promote repopulation and regeneration. This method is useful in the optimization of thread scaffolds, and is sensitive enough to distinguish between subtle variations in biopolymer chemistry and organization. Furthermore, this method was used to characterize the effects of crosslinking on the cell outgrowth and correlated the findings with the mechanical properties of collagen threads. The results suggest that crosslinking is required to achieve sufficient mechanical properties for high stress applications such as ACL replacement, but regardless of technique, crosslinking attenuated the cell outgrowth properties of the threads. To improve the regenerative capacity of these scaffolds, novel fibrin microthread matrices were developed with a similar morphology to collagen threads and sufficient mechanical strength to be incorporated in composite thread scaffold systems. These fibrin microthreads were loaded with FGF-2, a potent mitogen and chemotactic agent that works synergistically with fibrin in regulating cell signaling and gene expression. Increases in fibroblast migration and proliferation in FGF-2-loaded fibrin threads were successfully demonstrated with the concomitant promotion of oriented, aligned, spindle-like fibroblast morphology. These results suggest that fibrin-FGF-2 microthreads have distinct advantages as a biomaterial for the rapid regeneration of injured tissues such as the ACL.

Orientador: Prof. Dr. Arnaldo Rodrigues dos Santos Junior / Dissertação (mestrado) - Universidade Federal do ABC, Programa de Pós-Graduação em Biotecnociência, 2014. / Na engenharia de tecidos, a utilização de uma fonte de celular juntamente com um biomaterial, representa uma alternativa clínica a ser aplicada a pacientes com graves lesões no tecido ósseo. Este estudo teve como objetivo avaliar células Vero, uma linhagem de célula fibroblásticas, e uma linhagem de células-tronco mesenquimais (Rat (SD) Mesenchymal Stem Cells) em testes de biocompatibilidade in vitro com polímeros de poli(hidroxibutirato-co-hidroxivalerato) (PHBV), poli(caprolactona) (PCL) e blendas 75/25 e 50/50 desenvolvidos para a bioengenharia de tecido ósseo. A diferenciação osteogênica das CTMs sobre os polímeros também foi analisada. Os biomateriais foram caracterizados morfologicamente através de Microscopia Eletrônica de Varredura (MEV), Estereoscópio e Micrômetro. Polímeros porosos se mostram mais espesso que os densos. Através das imagens obtidas nota-se a distribuição, tamanho e morfologia dos poros, notando que os polímeros se mostram com características condizentes a de outros trabalhos. As células Vero e células-tronco mesenquimais (CTMs) foram cultivadas sobre as amostras citadas. Realizamos o ensaio com o MTT, análise morfológica e citoquímica. Para as CTMs fizemos ainda ensaios para avaliar a diferenciação osteogênica (fosfatase alcalina e vermelho alizarina). Nenhum dos polímeros foi considerado tóxico para as células Vero e na maioria deles foi notada atividade celular, camadas de células bem distribuídas. As blendas 50/50 mostraram resultados um pouco inferiores, quanto ao MTT, essa blenda porosa demonstrou ser a uma amostra onde adesão ocorre de forma bem mais lenta, os demais polímeros apresentaram resultados semelhantes e até superiores ao controle positivo de adesão, principalmente o PCL denso. Apesar das amostras 50/50 densa e porosa não se mostrarem tóxicas, aparentemente não funcionam com bons substratos como os demais polímeros, também apresentaram várias dificuldades na técnica de preparação, sendo assim descartadas. A relação das CTMs com os biomateriais se mostrou semelhante aos resultados com Vero. As células foram capazes de se espalhar por quase toda a superfície dos polímeros inclusive entre os poros dos materiais porosos. As CTMs apresentaram resultados de adesão (MTT) sobre os polímeros, mais rápido do que a Vero, demonstrando também maior afinidade pelo PCL denso. Através da análise da atividade da enzima fosfatase alcalina (usada como marcador de diferenciação), notamos que as células-tronco se mostraram capazes de se diferenciar em contato com os polímeros. Esses dados foram confirmados com o vermelho de alizarina, que também mostrou que a diferenciação celular se mostra um pouco mais lenta nos materiais do que nas placas. De uma forma geral os polímeros com exceção das blendas 50/50 se mostraram como bons substratos para as células, com ausência de toxicidade, características morfológicas dentro do recomendado e, além disso, não bloqueiam respostas biológicas específicas, como a diferenciação osteogênica. / In tissue engineering, the use of a cell source coupled with biomaterial represents a clinical alternative which can be applied to patients with severe bone damage. This study aimed to evaluate the biocompatibility between Vero a fibroblastic cell line and Mesenquymal stem cells (Rat (SD) MSC) with biomaterials developed as scaffolds for bone tissue engineering, bioresorbable polymers composed of poly ( hydroxybutyrate-co-hydroxyvalerate ) [ PHVB ] and poly ( caprolactone ) [ PCL ] pure and ratios of (75 /25) and (50 /50) blends. The osteogenic differentiation of MSCs on the polymers was also analyzed. Morphological characterization of the materials was performed by Scanning Electron Microscopy (SEM), Stereoscope and micrometer. The porous polymers are thicker than dense. Through the images obtained it is possible to note distribution, morphology and pore size. The biomaterials seem to the same consistent characteristics of other studies. Vero cells and mesenchymal stem cells (MSCs) were cultured on the samples mentioned. We performed the assay with MTT, morphological and histochemical analysis. About MSCs we also evaluated the osteogenic differentiation (alkaline phosphatase and Alizarin red). None of the polymers was considered toxic to Vero cells and most of them presented cellular activity, layers of well-distributed cells was noted in most of them. However 50/50 blends showed no such significant results as other. In the MTT assay, this porous blend demonstrated to be the only sample where adhesion occurs more slowly, other polymers showed similar and even higher results than the adhesion positive control, especially the dense PCL. Although the dense and porous 50/50 samples do not show toxic, apparently they are not good substrates as the other polymers, also presented several difficulties in their preparation thus being discarded. The ratio of MSCs with biomaterials was similar to the Vero cells results. They were able to spread to almost all surface of the polymers including into the pores of porous materials. MSCs showed adhesion (MTT) faster than the Vero cell, also demonstrated a greater affinity for dense PCL sample. Through analysis of the enzyme alkaline phosphatase activity (used as a marker for differentiation), we noticed that the stem cells showed differentiation into contact with the polymers. These data were confirmed by alizarin red, which also showed that the cell differentiation was slower on the materials than on the plates. In general all the polymer blends but the 50/50 proved to be good substrates for cells, with no toxicity, morphological characteristics within recommended and in addition do not block specific biological responses, such as osteogenic differentiation.

Made available in DSpace on 2016-06-02T20:19:05Z (GMT). No. of bitstreams: 1 1361.pdf: 7031010 bytes, checksum: e59579f600a182ade6d5f0cd26523978 (MD5) Previous issue date: 2007-02-27 / Universidade Federal de Sao Carlos / There is a rapid increase in the size of the elderly population due to a complex interaction of medical and epidemiological factors. Also, there is a parallel increase in morbidity associated with age-related delayed tendinopathy healing, and treatment of such acute and chronic condition costs the Health Services over 1 Billion dollars per year. Despite the obvious clinical impact, the basic cellular and molecular mechanisms underlying impaired human tendon healing are largely unknown. However, recent reports have showed the action mechanism of low level laser therapy (LLLT) in producing accelerated tendon healing, but the real effects of this therapy associated with aging effects are not yet known. This study evaluated the effects of the LLLT on repair process of rat calcaneal tendon in two different ages. Eighty male Wistar rats were divided in 2 experimental groups with 40 rats at each one: young group (4 weeks old, body mass = 111.3±34,3g) and mature adult group (27 weeks old, body mass = 385.4±34,3g). The young group was subdivided in subgroup Y3J (12 session, total energy = 101.7mJ, laser 685nm, 5.4W/cm2, 3J/cm2), subgroup Y10J (12 session, total energy = 339.6mJ, laser 685nm, 5.4W/cm2, 10J/cm2); subgroup YPL (placebo treatment) and subgroup YCL (no treatment). The mature adult group was subdivided in subgroup A3J (12 session, total energy = 101.7mJ, laser 685nm, 5.4W/cm2, 3J/cm2), subgroup A10J (12 session, total energy = 339.6mJ, laser 685nm, 5.4W/cm2, 10J/cm2); subgroup APL (placebo treatment) and subgroup ACL (no treatment). All animals had the medial region of right calcaneal tendon totally tenotomized. They were sacrified on the 13th post-operate day and their tendons were surgically removed for a quantitative and qualitative analysis The Atomic Force Microscopy analysis showed better organization quality (alignment, thickness and aggregation) of collagen bounds in mature irradiated groups. However, it was found differences (p < 0.05) in thickness of collagen bundles (TCBs) for several intersections among subgroups. The subgroup A10J presented greatest TCBs (5.69±0.69), and the ACL subgroup presented smallest TCBs (4.51±0.6) in the mature group. The dimensional data showed higher differences in the irradiated subgroup in mature group when compared to the same subgroup in young group. Histological analysis showed increase (p < 0.05) in the number of capillar vessels and fibroblast cell proliferation after LLLT in both young and mature groups, however the higher modulation was observed in the mature group. Minor influence of laser radiation in the young group may be justified by divergence on chemistry, physics and metabolic age-related. Maybe the accumulated oxidative stress resulting from a gradual shift in the redox status of tissues should be a key mechanism underlying the aging process and the higher laser effect noted in the mature group. Age should be considerated an important parameter to LLLT. / O envelhecimento biológico é uma das principais causas para a predisposição do tendão aos processos degenerativos, patológicos e retardo da reparação tecidual.Várias modalidades terapêuticas são utilizadas para promover a aceleração e melhora do reparo tendíneo, dentre elas a terapia laser de baixa intensidade (LLLT). Porém são pouco conhecidos os reais efeitos desta terapia quando se associa um fator potencialmente decisivo na resposta celular como o envelhecimento. Este estudo avaliou através de técnicas de microscopia de luz comum e de força atômica os efeitos da LLLT, aplicada na reparação do tendão calcanear em duas fases maturacionais. Um grupo de ratos jovens (4 semanas de idade, n = 40, massa = 111,3±8,3g), subdividido aleatoriamente em 4 subgrupos contendo cada um 10 animais: J3J (dose 3J/cm2, energia total = 101,7mJ), J10J (10J/cm2, energia total = 339,6mJ), placebo - JPL (dose 0J/cm2), controle - JCL (nenhum tratamento); e um grupo adulto (27 semanas de idade, n = 40, massa = 385,4±34,3g), subdividido aleatoriamente em 4 subgrupos: A3J (dose 3J/cm2, energia total = 101,7mJ), A10J (dose 10J/cm2, energia total = 339,6mJ), placebo - APL (dose 0J/cm2), controle - ACL (sem tratamento). Todos os animais foram submetidos ao procedimento de tenotomia radical do tendão direito, entre a inserção calcanear e a transição miotendínea, sem posterior tenorrafia. O laser utilizado (685nm, 5,4W/cm2) foi aplicado em 12 sessões, uma vez ao dia, em um único ponto sobre a região da lesão. No 13º dia pós-operatório os animais foram sacrificados e seus tendões removidos, processados e analisados qualitativa e quantitativamente, por meio de microscopia de força atômica (MFA) e análise histológica por morfometria. A análise dos dados mostrou significativa alteração (p< 0,05) da resposta do tecido à irradiação laser, tanto de forma idade-dependente como dose-dependente, sendo que, os resultados demonstram maior relevância para o grupo adulto que para o jovem. Comparativamente, o grupo adulto apresentou qualitativamente maior resposta biológica na agregação, organização, alinhamento do colágeno. Quantitativamente, o grupo adulto apresentou melhor resposta para a dose de 10J/cm2 principalmente em relação à angiogênese, contagem de fibroblastos e espessura dos feixes de colágeno. Esses resultados possivelmente podem ter uma relação com o maior estresse oxidativo característico ao incremento da idade.

Made available in DSpace on 2014-06-11T19:33:28Z (GMT). No. of bitstreams: 0 Previous issue date: 2005-06-06Bitstream added on 2014-06-13T19:23:26Z : No. of bitstreams: 1 ruiz_kgs_dr_arafo.pdf: 357284 bytes, checksum: 93541a495590ca3b701f6cf9ef876131 (MD5) / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) / O objetivo do presente estudo foi avaliar o efeito da combinação do fator de crescimento de fibroblastos básico (b-FGF) e fator de transformação de crescimento beta (TGF- beta) na proliferação, expressão de genes para colágeno tipos I e III, metaloproteases -1 e -2 e TIMPs 1, 2 e 3, e na síntese destes próprios fatores de crescimento pelas células do ligamento periodontal de humanos. A avaliação da proliferação celular foi realizada após os períodos de 24 e 48h na presença dos fatores de crescimento, através da mensuração do nível de MTS reduzido a formazan pelas células viáveis, e a síntese de b-FGF e TGF-b pelo teste ELISA empregando a técnica sandwich. Conclui-se que as associações do bFGF e do TGF-b atuaram de maneira dose-dependente no estímulo à proliferação celular, o aumento na expressão de genes para colágeno e TIMPs e redução para as metalproteases e modulação da síntese deles próprios. / The aim of this study was to evaluate the effect of association of basic fibroblast growth factor and transforming growth factor beta on the proliferation, expression of colagen type I e III, matrix metalloproteinases-1 e -2 e TIMPs 1, 2 e 3, and on the modulation of the syntheses oh these growth factors by humans periodontal ligament cells. The cellular proliferation was evaluated to 24 and 48 hours of incubation by the colorimetric method. The synthese of bFGF and TGF-ß was verificated by ELISA method, using a sandwich techinique, and mRNA expression by Real Time - PCR. In conlusion, the associations of bFGF e TGF-ß influenced of dose-dependent manner on the cellular proliferation, on the increasing of the expression to collagen and TIMPs, and on the reduction to metaloproteinases and, the modulation of these own synthesis.

Orientador: Ricardo Samih Georges Abi Rached / Banca: Silvana Regina Perez Orrico / Banca: Regina Maria Barretto Cicarelli / Banca: Francisco Humberto Nociti Junior / Banca: Márcio Zafallon Casati / Resumo: O objetivo do presente estudo foi avaliar o efeito da combinação do fator de crescimento de fibroblastos básico (b-FGF) e fator de transformação de crescimento beta (TGF- beta) na proliferação, expressão de genes para colágeno tipos I e III, metaloproteases -1 e -2 e TIMPs 1, 2 e 3, e na síntese destes próprios fatores de crescimento pelas células do ligamento periodontal de humanos. A avaliação da proliferação celular foi realizada após os períodos de 24 e 48h na presença dos fatores de crescimento, através da mensuração do nível de MTS reduzido a formazan pelas células viáveis, e a síntese de b-FGF e TGF-b pelo teste ELISA empregando a técnica "sandwich". Conclui-se que as associações do bFGF e do TGF-b atuaram de maneira dose-dependente no estímulo à proliferação celular, o aumento na expressão de genes para colágeno e TIMPs e redução para as metalproteases e modulação da síntese deles próprios. / Abstract: The aim of this study was to evaluate the effect of association of basic fibroblast growth factor and transforming growth factor beta on the proliferation, expression of colagen type I e III, matrix metalloproteinases-1 e -2 e TIMPs 1, 2 e 3, and on the modulation of the syntheses oh these growth factors by humans periodontal ligament cells. The cellular proliferation was evaluated to 24 and 48 hours of incubation by the colorimetric method. The synthese of bFGF and TGF-ß was verificated by ELISA method, using a "sandwich" techinique, and mRNA expression by Real Time - PCR. In conlusion, the associations of bFGF e TGF-ß influenced of dose-dependent manner on the cellular proliferation, on the increasing of the expression to collagen and TIMPs, and on the reduction to metaloproteinases and, the modulation of these own synthesis. / Doutor