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Olympus BX60

This model was found in 1,166 unique locations in 47 countries, where it was mentioned from 1996 until recently.

  • epifluorescent microscope
  • light microscope
  • fluorescence microscope
  • microscope
locations where this model was found
1,166
countries where the model is used
47
related research fields
173
first year this model was mentioned
1996

About the Olympus BX60

Questpair Analytics found the Olympus BX60 at 1,166 research organisations and laboratories in 47 countries, in publications from 1996 until recently. It is used most in Molecular Biology, General Medicine and Genetics.

Usage over time

Mentions per year, 1996–2020

2020 has the most mentions so far.

Research fields

173 related research fields

The Olympus BX60 is used by scientists in research fields such as Molecular Biology, General Medicine, Genetics, Cell Biology and Cancer Research.

  • Molecular Biology
  • General Medicine
  • Genetics
  • Cell Biology
  • Cancer Research
  • Immunology
  • Microbiology
  • Ecology, Evolution, Behavior and Systematics
  • General Biochemistry, Genetics and Molecular Biology
  • Oncology
  • Biochemistry
  • Immunology and Allergy
  • Molecular Medicine
  • Cellular and Molecular Neuroscience
  • General Neuroscience
  • General Materials Science
  • Plant Science
  • Biotechnology
  • Pathology and Forensic Medicine
  • Neurology (clinical)
  • General Chemistry
  • Spectroscopy
  • Organic Chemistry
  • Physical and Theoretical Chemistry
  • Biomaterials
  • Biomedical Engineering
  • Developmental Biology
  • Physiology
  • Microbiology (medical)
  • Pharmacology
  • + 143 more

Organisations using this equipment

The model was found at 1,166 locations in 47 countries.

1,166 locations in 47 countries
OrganisationInstrumentCityCountry
University of Plymouth
Olympus BX60MPlymouthUnited Kingdom
McGill University
Olympus BX60MQuébecCanada
University of Oxford
Olympus BX60MOxfordUnited Kingdom
Delft University of Technology
Olympus BX60MDelftNetherlands
Auckland University of Technology
Olympus BX60MAucklandNew Zealand
TU Dortmund University
Olympus BX60MDortmundGermany
7–12 of 1,166

Research that uses the Olympus BX60

Only abstracts that are published under Creative Commons Attribution 4.0 are shown on this page.

Evaluation of Fibroblast Viability Seeded on Acellular Human Amniotic Membrane

Background. Investigating the viability and proliferative rates of fibroblast cells on human amniotic membrane (HAM) as a scaffold will be an important subject for further research. The aim of this study was to assess the fibroblast viability seeded on acellular HAM, since foreskin neonatal allogenic fibroblasts seeded on HAM accelerate the wound healing process. Methods. Fibroblasts were retrieved from the foreskin of a genetically healthy male infant, and we exploited AM of healthy term neonates to prepare the amniotic scaffold for fibroblast transfer. After cell culture, preparation of acellular HAM, and seeding of cells on HAM based on the protocol, different methods including 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), 4,6-Diamidino-2-phenylindole dihydrochloride (DAPI), and propidium iodide (PI) staining were employed for assessment of fibroblast viability on HAM. Results. Based on the results obtained from the DAPI and PI staining, the percentage of viable cells in the former staining was clearly higher than that of the dead cells in the latter one. The results of DAPI and PI staining were in accordance with the findings of MTT assay, confirming that fibroblasts were viable and even proliferate on HAM. Conclusion. Our findings showed the viability of fibroblasts seeded on the acellular HAM using MTT assay, DAPI, and PI staining; however, this study had some limitations. It would be an interesting subject for future research to compare the viability and proliferation rate of fibroblasts seeded on both cellular and acellular HAM.

Hamideh Moravvej, Hamed Memariani, Mojtaba Memariani, Maryam Kabir-Salmani, Alireza Shoae-Hassani, Fahimeh Abdollahimajd. BioMed Research International, 2021, 1-6, 2021.

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Tailored microstructure and robust joint of Inconel 718/316L bimetallic multi-material fabricated by selective laser melting

In this study, selective laser melting (SLM) technology was used to fabricate Inconel 718/316L bimetallic multi-material with robust bonding strength, and a deep insight into the microstructural morphology, mechanical property and its strengthening mechanism of the joint was taken. The transition region with a wide of approximately 150 μm was defined and showed a dominating columnar region which was embedded in dispersed Laves phase occupied the molten of Inconel 718 closed to the joint. X-ray diffraction (XRD) pattern detected the strong peaks of γ', γ'' and a weaker peak of d phase precipitates. Electron backscatter diffraction (EBSD) analysis showed that a distinct grain coarsened region existing and Inconel 718 region had a strong fabric texture with a <001>// Z (BD) orientation. The shear strength of the as-built joint was calculated to be 449.5 MPa, which was comparable to the nickel/steel multi-materials formed by other traditional processing technologies.

Shifeng Wen, Keyu Chen, Yusi Che, Yang Liu, Jie Gan, Yan Zhou. 2020.

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Aß40 mutants protect Drosophila against Aß42 toxicity despite their amyloidogenic properties in the non-transgenic mouse brain

BackgroundSelf-assembly of the amyloid-β (Aβ) peptide into aggregates, from small oligomers to amyloid fibrils, is fundamentally linked with Alzheimer’s disease (AD). However it is clear that not all forms of Aβ are equally harmful, and that linking a specific aggregate to toxicity also depends on the assays and model systems used [1, 2]. Though a central postulate of the amyloid cascade hypothesis, there remain many gaps in our understanding regarding the links between Aβ deposition and neurodegeneration.MethodsIn this study, we examined familial mutations of Aβ that increase aggregation and oligomerization, E22G and DE22, and induce cerebral amyloid angiopathy, E22Q and D23N. We also investigated synthetic mutations that stabilize dimerization, S26C, and a phospho-mimetic, S8E, and non-phospho-mimetic, S8A. To that end, we utilized BRI2-Aβ fusion technology and rAAV2/1 based somatic brain transgenesis in mice to selectively express individual mutant Aβ species in vivo . In parallel we generated PhiC31-based transgenic Drosophila melanogaster expressing wild type (WT) and Aβ40 and Aβ42 mutants, fused to the Argos signal peptide to assess the extent of Aβ42-induced toxicity as well as to interrogate the combined effect of different Aβ40 and Aβ42 species.ResultsWhen expressed in the mouse brain for 6 months, Aβ42 E22G, Aβ42 E22Q/D23N, and Aβ42WT formed amyloid aggregates consisting of some diffuse material as well as cored plaques, whereas other mutants formed predominantly diffuse amyloid deposits. Moreover, while Aβ40WT showed no distinctive phenotype, Aβ40 E22G and E22Q/D23N formed unique aggregates that accumulated in mouse brains. This is the first evidence that mutant Aβ40 overexpression leads to deposition under certain conditions. Interestingly, we found that mutant Aβ42 E22G, E22Q, and S26C, but not Aβ40, were toxic to the eye of Drosophila . In contrast, flies expressing a copy of Aβ40 (WT or mutants) in addition to Aβ42WT, showed improved phenotypes, suggesting possible protective qualities for Aβ40.ConclusionsThese studies suggest that some Aβ40 mutants form unique amyloid aggregates in mouse brains, despite protecting against Aβ42 toxicity in Drosophila , which highlights the significance of using different systems for a better understanding of AD pathogenicity and more accurate screening for new potential therapies.

Lorena de Mena, Michael A Smith, Jason Martin, Katie L Dunton, Carolina Ceballos-Diaz, Karen Jansen-West, Pedro E Cruz, Kristy D Dillon, Diego Rincon-Limas, Todd E Golde, Brenda D Moore, Yona Levites. 2020.

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Global Deletion of the Prolactin Receptor Aggravates Streptozotocin-Induced Diabetes in Mice

Prolactin (PRL) levels are reduced in the circulation of rats with diabetes or obesity, and lower circulating levels of PRL correlate with increased prevalence of diabetes and a higher risk of metabolic alterations in the clinic. Furthermore, PRL stimulates β-cell proliferation, survival, and insulin production and pregnant mice lacking PRL receptors in β-cells develop gestational diabetes. To investigate the protective effect of endogenous PRL against diabetes outside pregnancy, we compared the number of cases and severity of streptozotocin (STZ)-induced hyperglycemia between C57BL/6 mice null for the PRL receptor gene (Prlr-/-) and wild-type mice (Prlr+/+). STZ-treated diabetic Prlr-/- mice showed a higher number of cases and later recovery from hyperglycemia, exacerbated glucose levels, and glucose intolerance compared to the Prlr+/+ mice counterparts. Consistent with the worsening of hyperglycemia, pancreatic islet density, β-cell number, proliferation, and survival, as well as circulating insulin levels were reduced, whereas α-cell number and pancreatic inflammation were increased in the absence of PRL signaling. Deletion of the PRL receptor did not alter the metabolic parameters in vehicle-treated animals. We conclude that PRL protects whole body glucose homeostasis by reducing β-cell loss and pancreatic inflammation in STZ-induced diabetes. Medications elevating PRL circulating levels may prove to be beneficial in diabetes.

Gabriela Ramirez-Hernandez, Elva Adan-Castro, Nundehui Diaz-Lezama, Xarubet Ruiz-Herrera, Gonzalo Martinez de la Escalera, Yazmin Macotela, Carmen Clapp. Frontiers in Endocrinology, 12, 2021.

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Counteracting the Negative Effects of Copper Limitations Through the Biostimulatory Action of a Tropical Plant Extract in Grapevine Under Pedo-Climatic Constraints

In southern Mediterranean areas, vineyards are facing the combination of increasing air temperature, drought and frequency of extreme events (e.g., heat waves) due to climate change. Since most of the berry growth and ripening phases occur during the aridity period, such environmental constraints are responsible for limitations in yield and berry quality. Within this scenario, to achieve vineyard sustainability, renewed approaches in vineyard management have been proposed and the use of plant biostimulants seems a prominent and environmental friendly practice. The aim of this study was to test four combinations of a tropical plant extract and conventional chemicals for disease control on morpho-anatomical, physiological, biochemical and berry quality in Vitis vinifera L. subsp. vinifera “Aglianico.” In particular, we aimed to evaluate the possibility to counteract the negative effects of the reductions in copper distribution, by applying the tropical plant extract enriched with: micronutrients, enzymes involved in the activation of natural defense, aminoacids, and vitamins. The halved dose of Cu in combination with the tropical plant extract allowed maintaining a reduced vegetative vigor. In the second year of treatment, the addition of the plant extract significantly improved leaf gas exchanges and photochemistry as well as the synthesis of photosynthetic pigments. At berry level, the plant extract induced an increase in phenolics accompanied by a decrease in soluble sugars. The overall results showed that the expected differences in growth performance and productivity in vines are linked to different eco-physiological and structural properties induced by the various treatments. The tropical plant extract also primed plant defenses at the leaf and fruit levels, mainly due to modifications of some structural and biochemical traits, respectively.

Chiara Cirillo, Carmen Arena, Youssef Rouphael, Rosanna Caputo, Chiara Amitrano, Francesca Petracca, Sara De Francesco, Ermenegilda Vitale, Arturo Erbaggio, Antonello Bonfante, Veronica De Micco. Frontiers in Environmental Science, 9, 2021.

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Effective Activation and Expansion of Canine Lymphocytes Using a Novel Nano-Sized Magnetic Beads Approach

Expansion protocols for human T lymphocytes using magnetic beads, which serve as artificial antigen presenting cells (aAPCs), is well-studied. Yet, the efficacy of magnetic beads for propagation and functionality of peripheral blood lymphocytes (PBLs) isolated from companion dogs still remains limited. Domestic dog models are important in immuno-oncology field. Thus, we built the platform for induction of canine PBLs function, proliferation and biological activity using nano-sized magnetic beads (termed as MicroBeads) coated with anti-canine CD3 and CD28 antibodies. Herein we reveal that activation of canine PBLs via MicroBeads induces a range of genes involved in immediate-early response to T cell activation in dogs. Furthermore, canine T lymphocytes are effectively activated by MicroBeads, as measured by cluster formation and induction of activation marker CD25 on canine T cells as quickly as 24 h post stimulation. Similar to human T cells, canine PBLs require lower activation signal strength for efficient proliferation and expansion, as revealed by titration studies using a range of MicroBeads in the culture. Additionally, the impact of temperature was assessed in multiple stimulation settings, showing that both 37°C and 38.5°C are optimal for the expansion of canine T cells. In contrast to stimulation using plant mitogen Concanavalin A (ConA), MicroBead-based activation did not increase activation-induced cell death. In turn, MicroBeads supported the propagation of T cells with an effector memory phenotype that secreted substantial IL-2 and IFN-γ. Thus, MicroBeads represent an accessible and affordable tool for conducting immunological studies on domestic dog models. Similarities in inducing intracellular signaling pathways further underscore the importance of this model in comparative medicine. Presented herein MicroBead-based expansion platforms for canine PBLs may benefit adoptive immunotherapy in dogs and facilitate the design of next-generation clinical trials in humans.

Iwona Monika Szopa, Monika Granica, Joanna Katarzyna Bujak, Agata Łabędź, Maciej Błaszczyk, Chrystal Mary Paulos, Kinga Majchrzak-Kuligowska. Frontiers in Immunology, 12, 2021.

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Remdesivir (GS-5734) Impedes Enterovirus Replication Through Viral RNA Synthesis Inhibition

Human enteroviruses are responsible for diverse diseases, from mild respiratory symptoms to fatal neurological complications. Currently, no registered antivirals have been approved for clinical therapy. Thus, a therapeutic agent for the enterovirus-related disease is urgently needed. Remdesivir (GS-5734) is a novel monophosphoramidate adenosine analog prodrug that exhibits potent antiviral activity against diverse RNA virus families, including positive-sense Coronaviridae and Flaviviridae and negative-sense Filoviridae, Paramyxoviridae, and Pneumoviridae. Currently, remdesivir is under phase 3 clinical development for disease COVID-19 treatment. Here, we found that remdesivir impeded both EV71 viral RNA (vRNA) and complementary (cRNA) synthesis, indicating that EV71 replication is inhibited by the triphosphate (TP) form of remdesivir. Moreover, remdesivir showed potent antiviral activity against diverse enteroviruses. These data extend the remdesivir antiviral activity to enteroviruses and indicate that remdesivir is a promising antiviral treatment for EV71 and other enterovirus infections.

Wei Ye, Min Yao, Yangchao Dong, Chuantao Ye, Dan Wang, He Liu, Hongwei Ma, Hui Zhang, Libin Qi, Yuewu Yang, Yuan Wang, Liang Zhang, Linfeng Cheng, Xin Lv, Zhikai Xu, Yingfeng Lei, Fanglin Zhang. Frontiers in Microbiology, 11, 2020.

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