journal
https://read.qxmd.com/read/34631910/a-method-for-the-efficient-iron-labeling-of-patient-derived-xenograft-cells-and-cellular-imaging-validation
#21
JOURNAL ARTICLE
Natasha N Knier, Veronica P Dubois, Yuanxin Chen, John A Ronald, Paula J Foster
There is momentum towards implementing patient-derived xenograft models (PDX) in cancer research to reflect the histopathology, tumor behavior, and metastatic properties observed in the original tumor. To study PDX cells preclinically, we used both bioluminescence imaging (BLI) to evaluate cell viability and magnetic particle imaging (MPI), an emerging imaging technology to allow for detection and quantification of iron nanoparticles. The goal of this study was to develop the first successful iron labeling method of breast cancer cells derived from patient brain metsastases and validate this method with imaging during tumor development...
2021: Journal of Biological Methods
https://read.qxmd.com/read/34631909/getting-two-birds-with-one-stone-combining-immunohistochemistry-and-azan-staining-in-animal-morphology
#22
JOURNAL ARTICLE
Patrick Beckers, Claudia Müller, Christiane Wallnisch, Thomas Bartolomaeus
Classical histological stained sections have the disadvantage that fine structures, like individual neurites, or specific macromolecules, like neurotransmitters cannot be visualized. Due to its highly specific staining of only one target molecule within the cell, the visualization of delicate structures, which would be superimposed by other tissue layers in classical Azan staining, is possible with immunohistochemistry. However, using immunohistological methods not all tissues of a specimen can be visualized at once...
2021: Journal of Biological Methods
https://read.qxmd.com/read/34514013/tissue-specific-damid-protocol-using-nanopore-sequencing
#23
JOURNAL ARTICLE
Georgina Gómez-Saldivar, Dominique A Glauser, Peter Meister
DNA adenine methylation identification (DamID) is a powerful method to determine DNA binding profiles of proteins at a genomic scale. The method leverages the fusion between a protein of interest and the Dam methyltransferase of E. coli , which methylates proximal DNA in vivo . Here, we present an optimized procedure, which was developed for tissue-specific analyses in Caenorhabditis elegans and successfully used to footprint genes actively transcribed by RNA polymerases and to map transcription factor binding in gene regulatory regions...
2021: Journal of Biological Methods
https://read.qxmd.com/read/34514012/comparison-of-crispr-and-adenovirus-mediated-myd88-knockdown-in-raw-264-7-cells-and-responses-to-lipopolysaccharide-stimulation
#24
JOURNAL ARTICLE
Alexander L Kolb, Marinaliz Reynoso, Ronald W Matheny
Genomic manipulation offers the possibility for novel therapies in lieu of medical interventions in use today. The ability to genetically restore missing inflammatory genes will have a monumental impact on our current immunotherapy treatments. This study compared the efficacy of two different genetic manipulation techniques: clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR associated protein 9 (Cas9) transfection to adenoviral transduction to determine which method would provide the most transient and stable knockdown of myeloid differentiation primary response 88 (MyD88)...
2021: Journal of Biological Methods
https://read.qxmd.com/read/34258308/an-efficient-method-to-generate-kidney-organoids-at-the-air-liquid-interface
#25
JOURNAL ARTICLE
Ashwani Kumar Gupta, David Z Ivancic, Bilal A Naved, Jason A Wertheim, Leif Oxburgh
The prevalence of kidney dysfunction continues to increase worldwide, driving the need to develop transplantable renal tissues. The kidney develops from four major renal progenitor populations: nephron epithelial, ureteric epithelial, interstitial and endothelial progenitors. Methods have been developed to generate kidney organoids but few or dispersed tubular clusters within the organoids hamper its use in regenerative applications. Here, we describe a detailed protocol of asynchronous mixing of kidney progenitors using organotypic culture conditions to generate kidney organoids tightly packed with tubular clusters and major renal structures including endothelial network and functional proximal tubules...
2021: Journal of Biological Methods
https://read.qxmd.com/read/34258307/assessment-of-galactose-1-phosphate-uridyltransferase-activity-in-cells-and-tissues
#26
JOURNAL ARTICLE
Megan L Brophy, John E Murphy, Robert D Bell
Galactosemias are a family of autosomal recessive genetic disorders resulting from impaired enzymes of the Leloir pathway of galactose metabolism including galactokinase, galactose uridyltransferase, and UDP-galactose 4-epimerase that are critical for conversion of galactose into glucose-6-phosphate. To better understand pathophysiological mechanisms involved in galactosemia and develop novel therapies to address the unmet need in patients, it is important to develop reliable assays to measure the activity of the Leloir pathway enzymes...
2021: Journal of Biological Methods
https://read.qxmd.com/read/34104665/-in-vitro-fermentation-test-bed-for-evaluation-of-engineered-probiotics-in-polymicrobial-communities
#27
JOURNAL ARTICLE
Steven Arcidiacono, Amy M Ehrenworth Breedon, Michael S Goodson, Laurel A Doherty, Wanda Lyon, Grace Jimenez, Ida G Pantoja-Feliciano, Jason W Soares
In vitro fermentation systems offer significant opportunity for deconvoluting complex metabolic dynamics within polymicrobial communities, particularly those associated with the human gut microbiome. In vitro gut models have broad experimental capacity allowing rapid evaluation of multiple parameters, generating knowledge to inform design of subsequent in vivo studies. Here, our method describes an in vitro fermentation test bed to provide a physiologically-relevant assessment of engineered probiotics circuit design functions...
2021: Journal of Biological Methods
https://read.qxmd.com/read/34104664/virtual-screening-on-the-web-for-drug-repurposing-a-primer
#28
JOURNAL ARTICLE
Yu Wai Chen, Chin-Pang Bennu Yiu, Kwok-Yin Wong
We describe a procedure of performing in silico (virtual) screening using a web-based service, the MTiOpenScreen, which is freely accessible to non-commercial users. We shall use the SARS-CoV-2 main protease as an example. Starting from a structure downloaded from the Protein Data Bank, we discuss how to prepare the coordinates file, taking into account the known biochemical background information of the target protein. The reader will find that this preparation step takes up most of the effort before the target is ready for screening...
2021: Journal of Biological Methods
https://read.qxmd.com/read/33889653/fabricating-spatially-functionalized-3d-printed-scaffolds-for-osteochondral-tissue-engineering
#29
JOURNAL ARTICLE
Paula Camacho, Matthew Fainor, Kelly B Seims, John W Tolbert, Lesley W Chow
Three-dimensional (3D) printing of biodegradable polymers has rapidly become a popular approach to create scaffolds for tissue engineering. This technique enables fabrication of complex architectures and layer-by-layer spatial control of multiple components with high resolution. The resulting scaffolds can also present distinct chemical groups or bioactive cues on the surface to guide cell behavior. However, surface functionalization often includes one or more post-fabrication processing steps, which typically produce biomaterials with homogeneously distributed chemistries that fail to mimic the biochemical organization found in native tissues...
2021: Journal of Biological Methods
https://read.qxmd.com/read/33889652/high-yield-purification-of-exceptional-quality-single-molecule-dna-substrates
#30
JOURNAL ARTICLE
Yue Lu, Piero Bianco
Single-molecule studies involving DNA or RNA, require homogeneous preparations of nucleic acid substrates of exceptional quality. Over the past several years, a variety of methods have been published describing different purification methods but these are frustratingly inconsistent with variable yields even in the hands of experienced bench scientists. To address these issues, we present an optimized and straightforward, column-based approach that is reproducible and produces high yields of substrates or substrate components of exceptional quality...
2021: Journal of Biological Methods
https://read.qxmd.com/read/33604396/using-a-variant-of-the-optomotor-response-as-a-visual-defect-detection-assay-in-zebrafish
#31
JOURNAL ARTICLE
Matthew K LeFauve, Cassie J Rowe, Mikayla Crowley-Perry, Jenna L Wiegand, Arthur G Shapiro, Victoria P Connaughton
We describe a visual stimulus that can be used with both larval and adult zebrafish (Danio rerio). This protocol is a modification of a standard visual behavior analysis, the optomotor response (OMR). The OMR is often used to determine the spatial response or to detect directional visuomotor deficiencies. An OMR can be generated using a high contrast grated pattern, typically vertical bars. The spatial sensitivity is measured by detection and response to a change in grating bar width and is reported in cycles per degree (CPD)...
2021: Journal of Biological Methods
https://read.qxmd.com/read/33604395/optimization-of-small-scale-sample-preparation-for-high-throughput-openarray-analysis
#32
JOURNAL ARTICLE
Neeta A Abraham, Anne C Campbell, Warren D Hirst, Catherine L Nezich
OpenArray is one of the most high-throughput qPCR platforms available but its efficiency can be limited by sample preparation methods that are slow and costly. To optimize the sample workflow for high-throughput qPCR processing by OpenArray, small-scale sample preparation methods were compared for compatibility with this system to build confidence in a method that maintains quality and accuracy while using less starting material and saving time and money. This study is the first to show that the Cells-to-CT kit can be used to prepare samples within the dynamic range of OpenArray directly from cultured cells in a single well of a 96-well plate when used together with a cDNA preamplification PCR step...
2021: Journal of Biological Methods
https://read.qxmd.com/read/33604394/visualization-of-subdiffusive-sites-in-a-live-single-cell
#33
JOURNAL ARTICLE
Zeno Földes-Papp, Gerd Baumann, Long-Cheng Li
We measured anomalous diffusion in human prostate cancer cells which were transfected with the Alexa633 fluorescent RNA probe and co-transfected with enhanced green fluorescent protein-labeled argonaute2 protein by laser scanning microscopy. The image analysis arose from diffusion based on a "two-level system". A trap was an interaction site where the diffusive motion was slowed down. Anomalous subdiffusive spreading occurred at cellular traps. The cellular traps were not immobile. We showed how the novel analysis method of imaging data resulted in new information about the number of traps in the crowded and heterogeneous environment of a single human prostate cancer cell...
2021: Journal of Biological Methods
https://read.qxmd.com/read/33564693/comparison-of-different-clearing-and-acquisition-methods-for-3d-imaging-of-murine-intestinal-organoids
#34
JOURNAL ARTICLE
Louison Lallemant, Corinne Lebreton, Meriem Garfa-Traoré
An organoid is a three-dimensional multicellular structure that shows realistic micro-anatomy of an organ. This in vitro model mimics the in vivo environment, architecture and multi-lineage differentiation of the original organs and allows to answer many interesting biological questions. For these reasons, they are widely used in stem cell, regenerative medicine, toxicology, pharmacology, and host-microbe interactions research. In order to study organoids, microscopy is very useful: It is possible to make three-dimensional reconstruction of serial sections but it is time consuming and error-prone...
2020: Journal of Biological Methods
https://read.qxmd.com/read/33564692/a-streamlined-crispr-cas9-approach-for-fast-genome-editing-in-toxoplasma-gondii-and-besnoitia-besnoiti
#35
JOURNAL ARTICLE
Rahel R Winiger, Adrian B Hehl
Toxoplasma gondii ( T. gondii ) and Besnoitia besnoiti ( B. besnoiti ) are closely related coccidian parasites belonging to the phylum Apicomplexa, which comprises many other important pathogens of humans and livestock. T. gondii is considered a model organism for studying the cell biology of Apicomplexa mainly due to the ease of propagation in diverse host cells and the availability of a wide range of genetic tools. Conversely, B. besnoiti in vitro culture systems currently exist only for the acute phase of infection, and genetic manipulation has proven much more challenging...
2020: Journal of Biological Methods
https://read.qxmd.com/read/33204742/an-adapted-novel-flow-cytometry-methodology-to-delineate-types-of-cell-death-in-airway-epithelial-cells
#36
JOURNAL ARTICLE
Samuel T Montgomery, Stephen M Stick, Anthony Kicic
Current methodologies to measure apoptotic and necrotic cell death using flow cytometry do not adequately differentiate between the two. Here, we describe a flow cytometry methodology adapted to airway epithelial cells (AEC) to sufficiently differentiate apoptotic and necrotic AEC. Specifically, cell lines and primary AEC ( n = 12) were permeabilized or infected with rhinovirus 1b (RV1b) over 48 h. Cell death was then measured via annexin V/propidium iodide (A5/PI) or annexin V/TO-PRO-3 (A5/TP3) staining using a novel flow cytometry and gating methodology adapted to AEC...
2020: Journal of Biological Methods
https://read.qxmd.com/read/33204741/an-ex-vivo-skin-model-to-probe-modulation-of-local-cutaneous-arachidonic-acid-inflammation-pathway
#37
REVIEW
Charles M Heard
There is a need for inexpensive and reliable means to determine the modulation of cutaneous inflammation. The method outlined in this article draws together a number of scientific techniques and makes use of generally unwanted biological tissues as a means of determining skin inflammation ex vivo , and focuses on probing aspects of the arachidonic acid inflammation pathway. Freshly excised skin contains elevated levels of short-lived inducible cyclooxygenase-2 (COX-2) and, under viable conditions, COX-2 and its eicosanoid products will continue to be produced until tissue necrosis, providing a window of time in which relative levels can be probed to determine exacerbation due to an upregulating factor or downregulation due the presence of an agent exerting anti-inflammatory activity...
2020: Journal of Biological Methods
https://read.qxmd.com/read/33204740/a-simplified-design-for-the-c-elegans-lifespan-machine
#38
JOURNAL ARTICLE
Mark Abbott, Stephen A Banse, Ilija Melentijevic, Cody M Jarrett, Jonathan St Ange, Christine A Sedore, Ron Falkowski, Benjamin W Blue, Anna L Coleman-Hulbert, Erik Johnson, Max Guo, Gordon J Lithgow, Patrick C Phillips, Monica Driscoll
Caenorhabditis elegans ( C. elegans ) lifespan assays constitute a broadly used approach for investigating the fundamental biology of longevity. Traditional C. elegans lifespan assays require labor-intensive microscopic monitoring of individual animals to evaluate life/death over a period of weeks, making large-scale high throughput studies impractical. The lifespan machine developed by Stroustrup et al . (2013) adapted flatbed scanner technologies to contribute a major technical advance in the efficiency of C...
2020: Journal of Biological Methods
https://read.qxmd.com/read/33204739/a-simple-and-robust-cell-based-assay-for-the-discovery-of-novel-cytokinesis-inhibitors
#39
JOURNAL ARTICLE
Laszlo Radnai, Rebecca F Stremel, Thomas Vaissiere, Li Lin, Michael Cameron, William H Martin, Gavin Rumbaugh, Theodore M Kamenecka, Patrick R Griffin, Courtney A Miller
Cytokinesis is the last step of mitotic cell division that separates the cytoplasm of dividing cells. Small molecule inhibitors targeting either the elements of the regulatory pathways controlling cytokinesis, or the terminal effectors have been of interest as potential drug candidates for the treatment of various diseases. Here we present a detailed protocol for a cell-based cytokinesis assay that can be used for the discovery of novel cytokinesis inhibitors. The assay is performed in a 96-well plate format in 48 h...
2020: Journal of Biological Methods
https://read.qxmd.com/read/32934967/an-in-vitro-model-of-hepatic-steatosis-using-lipid-loaded-induced-pluripotent-stem-cell-derived-hepatocyte-like-cells
#40
JOURNAL ARTICLE
Hiraganahalli Bhaskar Deepak, Nellikalaya Shreekrishna, Zaheerbasha Sameermahmood, Niranjan Naranapur Anand, Raghotham Hulgi, Juluri Suresh, Sonal Khare, Saravanakumar Dhakshinamoorthy
Hepatic steatosis is a metabolic disease, characterized by selective and progressive accumulation of lipids in liver, leading to progressive non-alcoholic fatty liver disease (NAFLD), non-alcoholic steatohepatitis (NASH), and cirrhosis. The existing in vitro models of hepatic steatosis to elucidate the molecular mechanisms behind the onset of hepatic steatosis and to profile small molecule modulators uses lipid loaded primary hepatocytes, and cell lines like HepG2. The limitation of these models includes high variability between the different donor samples, reproducibility, and translatability to physiological context...
2020: Journal of Biological Methods
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