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1.
Plant Biol (Stuttg) ; 21(6): 1110-1118, 2019 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-31173441

RESUMO

Seedling establishment is a critical step in environment colonisation by higher plants that frequently occurs under adverse conditions. Thus, we carried out an integrated analysis of seedling growth, water status, ion accumulation, reserve mobilisation, metabolite partitioning and hydrolase activity during seedling establishment of the native Caatinga species Piptadenia moniliformis (Benth.) Luckow & R.W. Jobson under salinity. Two-day-old seedlings were cultivated in vitro for 4 days in water agar (control) or supplemented with 50 or 100 mm NaCl. Biochemical determinations were performed according to standard spectrophotometric protocols. We found that 100 mm NaCl stimulated starch degradation, amylase activity and soluble sugar accumulation, but limited storage protein hydrolysis in the cotyledons of P. moniliformis seedlings. Although Na+ accumulation in the seedling affected K+ partitioning between different organs, it was not possible to associate the salt-induced changes in reserve mobilisation with Na+ toxicity, or water status, in the cotyledons. Remarkably, we found that starch content increased in the roots of P. moniliformis seedlings under 100 mm NaCl, probably in response to the toxic effects of Na+ . The mobilisation of carbon and nitrogen reserves is independently regulated in P. moniliformis seedlings under salt stress. The salt-induced delay in seedling establishment and the resulting changes in the source-sink relationship may lead to storage protein retention in the cotyledons. Possibly, the intensification of starch mobilisation in the cotyledons supported starch accumulation in the root as a potential mechanism to mitigate Na+ toxicity.


Assuntos
Carbono/metabolismo , Moniliformis/metabolismo , Nitrogênio/metabolismo , Plântula/metabolismo , Animais , Cotilédone/efeitos dos fármacos , Cotilédone/metabolismo , Moniliformis/efeitos dos fármacos , Salinidade , Plântula/efeitos dos fármacos , Sódio/metabolismo , Cloreto de Sódio/farmacologia
2.
Plant Biol (Stuttg) ; 19(3): 335-344, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-28039918

RESUMO

Reserve mobilisation, metabolite partitioning and reserve-degrading enzyme activity were studied in sunflower seedlings cultivated in vitro under a 12-h photoperiod or in the dark to investigate the involvement of source-sink relation and carbon starvation in the regulation of reserve mobilisation under continuous darkness. Reserves, metabolites and enzyme activity were determined with standard spectrophotometric methods. At the first 24 h of treatment (acclimation phase), darkness did not affect growth, but restricted carbon and nitrogen use, as indicated by sugar and amino acid accumulation in the different seedling parts. After 5 days of treatment (survival phase), extended darkness limited growth and retarded storage lipid mobilisation due to carbon starvation, as evidenced by the depletion of carbohydrates in cotyledons and hypocotyl, as well as the consumption of amino acids in hypocotyls and roots. Alterations in the source-sink relationship might have been a response to prolonged darkness, instead of a mechanism used to regulate reserve mobilisation, as these alterations cannot be associated with negative feedback mediated by metabolite accumulation. Storage lipid degradation depends, at least in part, on mechanisms that co-ordinately regulate the activities of lipases and isocitrate lyase. Taking these results together, it is possible that reserve mobilisation in sunflower seedlings cultivated in the dark might be regulated by mechanisms that perceive the absence of light and predict carbon starvation, adjusting reserve use according to future energy demands to allow, at least in the short term, seedling survival.


Assuntos
Enzimas/metabolismo , Helianthus/fisiologia , Plântula/crescimento & desenvolvimento , Plântula/metabolismo , Carbono/metabolismo , Carotenoides/metabolismo , Clorofila/metabolismo , Cotilédone/crescimento & desenvolvimento , Escuridão , Metabolismo dos Lipídeos , Fotoperíodo , Proteínas de Plantas/metabolismo , Raízes de Plantas/crescimento & desenvolvimento , Plântula/fisiologia
3.
J Periodontal Res ; 51(5): 577-85, 2016 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26564991

RESUMO

BACKGROUND AND OBJECTIVE: Protease activated receptor type 1 (PAR1 ) seems to play a role in periodontal repair, while PAR2 is associated with periodontal inflammation. As diabetes is a known risk factor for periodontal disease, the aim of this study was to evaluate the influence of type 2 diabetes on PAR1 and PAR2 mRNA expression in the gingival crevicular fluid of patients with chronic periodontitis before and after non-surgical periodontal treatment. MATERIAL AND METHODS: Gingival crevicular fluid samples and clinical parameters consisting of measuring probing depth, clinical attachment level, bleeding on probing and plaque index were collected from systemically healthy patients and patients with type 2 diabetes and chronic periodontitis, at baseline and after non-surgical periodontal therapy. PAR1 and PAR2 , as well as the presence of the proteases RgpB gingipain and neutrophil proteinase-3 were assessed by quantitative polymerase chain reaction in the gingival crevicular fluid. RESULTS: The periodontal clinical parameters significantly improved after periodontal therapy (p < 0.01). Diabetes led to increased expression of PAR1 in gingival crevicular fluid, and in the presence of chronic periodontitis, it significantly decreased the expression of PAR1 and PAR2 (p < 0.05). Moreover, non-surgical periodontal treatment in diabetics resulted in increased expression of PAR1 and PAR2 (p < 0.05), and decreased expression of RgpB gingipain and proteinase-3 (p < 0.05). CONCLUSION: The present data demonstrated that diabetes was associated with an altered expression of PAR1 and PAR2 in the gingival crevicular fluid cells of subjects with chronic periodontitis. Future studies are necessary to elucidate the effects of PAR1 upregulation in periodontally healthy sites and PAR2 downregulation in chronic periodontitis sites on the increased susceptibility and severity of periodontitis in diabetes.


Assuntos
Periodontite Crônica/metabolismo , Diabetes Mellitus Tipo 2/metabolismo , Líquido do Sulco Gengival/química , Receptor PAR-1/análise , Receptor PAR-2/análise , Adulto , Periodontite Crônica/complicações , Periodontite Crônica/terapia , Índice de Placa Dentária , Diabetes Mellitus Tipo 2/complicações , Feminino , Fibroblastos/química , Humanos , Masculino , Pessoa de Meia-Idade , Mieloblastina/análise , Mieloblastina/genética , Mieloblastina/metabolismo , Perda da Inserção Periodontal , Bolsa Periodontal , RNA Mensageiro/biossíntese , Receptor PAR-1/genética , Receptor PAR-1/metabolismo , Receptor PAR-2/genética , Receptor PAR-2/metabolismo , Fatores de Risco
4.
Clin Oral Implants Res ; 20(3): 288-93, 2009 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19397640

RESUMO

OBJECTIVES: In regenerative medicine, surface engineering of bioinert synthetic materials is often required in order to introduce bioactive species that can promote cell adhesion, proliferation, viability and enhanced ECM-secretion functions. The aim of this work is to study cell interaction with alumina-modified surfaces. MATERIAL AND METHODS: In this work, chemical properties of alumina surface were changed by a reaction at the surface of alumina with low molecular weight dicarboxylic acid, which produced carboxyl groups. RESULTS: These carboxyl groups were able to complex with Ca2+ on the surface, forming sites of precipitation for calcium phosphates that make alumina biocompatible, as indicated by cell culture of pre-osteoblasts (MC3T3-E1 cell line). CONCLUSIONS: The procedure presented in this work shows that the insertion of specific functional groups on the surface of alumina increases cell interaction with the surface of alumina. This knowledge can be important in oral science and orthopedics, for the construction of prosthesis.


Assuntos
Alumínio/química , Materiais Biocompatíveis/química , Cálcio/química , Dióxido de Carbono/química , Osteoblastos/efeitos dos fármacos , Alumínio/farmacologia , Animais , Materiais Biocompatíveis/farmacologia , Dióxido de Carbono/farmacologia , Adesão Celular/efeitos dos fármacos , Diferenciação Celular/efeitos dos fármacos , Sobrevivência Celular/efeitos dos fármacos , Fibroblastos/citologia , Fibroblastos/efeitos dos fármacos , Camundongos , Osteoblastos/citologia , Propriedades de Superfície
5.
Nature ; 375(6534): 754-60, 1995 Jun 29.
Artigo em Inglês | MEDLINE | ID: mdl-7596406

RESUMO

Some cases of Alzheimer's disease are inherited as an autosomal dominant trait. Genetic linkage studies have mapped a locus (AD3) associated with susceptibility to a very aggressive form of Alzheimer's disease to chromosome 14q24.3. We have defined a minimal cosegregating region containing the AD3 gene, and isolated at least 19 different transcripts encoded within this region. One of these transcripts (S182) corresponds to a novel gene whose product is predicted to contain multiple transmembrane domains and resembles an integral membrane protein. Five different missense mutations have been found that cosegregate with early-onset familial Alzheimer's disease. Because these changes occurred in conserved domains of this gene, and are not present in normal controls, they are likely to be causative of AD3.


Assuntos
Doença de Alzheimer/genética , Cromossomos Humanos Par 14 , Clonagem Molecular , Proteínas de Membrana/genética , Mutação , Sequência de Aminoácidos , Animais , Sequência de Bases , Mapeamento Cromossômico , Feminino , Humanos , Masculino , Proteínas de Membrana/química , Camundongos , Dados de Sequência Molecular , Fases de Leitura Aberta , Linhagem , Presenilina-1 , Estrutura Secundária de Proteína , Transcrição Gênica
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