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1.
J Bone Miner Res ; 39(2): 177-189, 2024 Mar 22.
Artigo em Inglês | MEDLINE | ID: mdl-38477760

RESUMO

Bone histomorphometry is a well-established approach to assessing skeletal pathology, providing a standard evaluation of the cellular components, architecture, mineralization, and growth of bone tissue. However, it depends in part on the subjective interpretation of cellular morphology by an expert, which introduces bias. In addition, diseases like osteogenesis imperfecta (OI) and fibrous dysplasia are accompanied by changes in the morphology and function of skeletal tissue and cells, hindering consistent evaluation of some morphometric parameters and interpretation of the results. For instance, traditional histomorphometry combined with collagen turnover markers suggested that reduced bone formation in classical OI is accompanied by increased bone resorption. In contrast, the well-documented postpubertal reduction in fractures would be easier to explain by reduced bone resorption after puberty, highlighting the need for less ambiguous measurements. Here we propose an approach to histomorphometry based on in situ mRNA hybridization, which uses Col1a1 as osteoblast and Ctsk as osteoclast markers. This approach can be fully automated and eliminates subjective identification of bone surface cells. We validate these markers based on the expression of Bglap, Ibsp, and Acp5. Comparison with traditional histological and tartrate-resistant acid phosphatase staining of the same sections suggests that mRNA-based analysis is more reliable. Unlike inconclusive traditional histomorphometry of mice with α2(I)-Gly610 to Cys substitution in the collagen triple helix, mRNA-based measurements reveal reduced osteoclastogenesis in 11-wk-old animals consistent with the postpubertal catch-up osteogenesis observed by microCT. We optimize the technique for cryosections of mineralized bone and sections of paraffin-embedded decalcified tissue, simplifying and broadening its applications. We illustrate the application of the mRNA-based approach to human samples using the example of a McCune-Albright syndrome patient. By eliminating confounding effects of altered cellular morphology and the need for subjective morphological evaluation, this approach may provide a more reproducible and accessible evaluation of bone pathology.


Assuntos
Osso e Ossos , Colágeno Tipo I , Modelos Animais de Doenças , Osteogênese Imperfeita , Osteogênese Imperfeita/patologia , Osteogênese Imperfeita/metabolismo , Osteogênese Imperfeita/genética , Animais , Camundongos , Osso e Ossos/patologia , Osso e Ossos/metabolismo , Colágeno Tipo I/metabolismo , Colágeno Tipo I/genética , Cadeia alfa 1 do Colágeno Tipo I , RNA Mensageiro/metabolismo , RNA Mensageiro/genética , Osteoclastos/metabolismo , Osteoclastos/patologia , Puberdade , Osteoblastos/metabolismo , Osteoblastos/patologia , Biomarcadores/metabolismo , Osteogênese
2.
ISME J ; 15(9): 2643-2654, 2021 09.
Artigo em Inglês | MEDLINE | ID: mdl-33746203

RESUMO

Demographic noise, the change in the composition of a population due to random birth and death events, is an important driving force in evolution because it reduces the efficacy of natural selection. Demographic noise is typically thought to be set by the population size and the environment, but recent experiments with microbial range expansions have revealed substantial strain-level differences in demographic noise under the same growth conditions. Many genetic and phenotypic differences exist between strains; to what extent do single mutations change the strength of demographic noise? To investigate this question, we developed a high-throughput method for measuring demographic noise in colonies without the need for genetic manipulation. By applying this method to 191 randomly-selected single gene deletion strains from the E. coli Keio collection, we find that a typical single gene deletion mutation decreases demographic noise by 8% (maximal decrease: 81%). We find that the strength of demographic noise is an emergent trait at the population level that can be predicted by colony-level traits but not cell-level traits. The observed differences in demographic noise from single gene deletions can increase the establishment probability of beneficial mutations by almost an order of magnitude (compared to in the wild type). Our results show that single mutations can substantially alter adaptation through their effects on demographic noise and suggest that demographic noise can be an evolvable trait of a population.


Assuntos
Escherichia coli , Seleção Genética , Escherichia coli/genética , Mutação , Fenótipo , Densidade Demográfica
3.
Animals (Basel) ; 9(4)2019 Apr 05.
Artigo em Inglês | MEDLINE | ID: mdl-30959748

RESUMO

Pig producers are required to provide environmental enrichment to provide pigs the opportunity to perform investigative and manipulative behaviours (EU directive 2001/93/EC). Preventing enrichment from losing its novelty and decreasing the rate at which animals become habituated is important to maintain use of enrichment over time. A comparative study was formulated to identify whether weaner pigs housed in a semi-barren environment displayed a preference for olfactory enrichment compared to non-scented enrichment. Pigs (n = 146) were selected at 28 days old from two different batches (n = 76 and n = 70) and divided into pens. All pigs were given a control and a treatment (garlic scented) rope. Behavioural observations and rope interactions were assessed through direct observation. Throughout the entire study, the length of interaction with the garlic device was significantly higher (p < 0.02), indicating that there was a preference for olfactory enrichment compared to an odourless device. There was no significant occurrence of tail, ear, or flank biting in both batches. Weaner pigs showed a preference towards olfactory enrichment. Although habituation began to occur, this effect was mitigated by re-spraying the ropes, which resulted in increased interactions.

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