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kidney cells

Identification of Candidate PAX2-Regulated Genes Implicated in Human Kidney Development

[Scientific Reports] Scientists hypothesized that key human PAX2-dependent kidney development genes are differentially expressed in nephron progenitor cells from induced pluripotent stem cells in patients with renal coloboma syndrome relative to healthy individuals.

Lithocholic Bile Acid Induces Apoptosis in Human Nephroblastoma Cells: A Non-Selective Treatment Option

[Scientific Reports] Scientists evaluated the effects of Lithocholic bile acid (LCA) on nephroblastoma. To test the effects of LCA, nephroblastoma cell line WT CLS1 was used.

Artificial Cells Drive Neural Differentiation

[Science Advances] Scientists suggested that artificial cells were a versatile chassis for the in situ synthesis and on-demand release of chemical signals that elicited desired phenotypic changes of eukaryotic cells, including neuronal differentiation.

T-Type Calcium Channel Antagonist, TTA-A2 Exhibits Anti-Cancer Properties in 3D Spheroids of A549, a Lung Adenocarcinoma Cell Line

[Life Sciences] Scientists studied TTA-A2 and paclitaxel in lung adenocarcinoma cell line- A549, cancer cells and human embryonic kidney cell line- HEK 293, control cell, in their monolayer and spheroids forms for viability, proliferation, morphology change, migration, and invasion-after 48–96 hours of treatment.

Formation and Optimization of Three-Dimensional Organoids Generated From Urine-Derived Stem Cells for Renal Function In Vitro

[Stem Cell Research & Therapy] Researchers aimed to develop a novel kind of 3D organoids generated from urine-derived stem cells and to explore whether kidney-specific extracellular matrix could enable such organoids for renal function in vitro.

Macrophage Metabolic Reprogramming Presents a Therapeutic Target in Lupus Nephritis

[Proceedings of the National Academy of Sciences of the United States of America] Investigators found that human and mouse macrophages underwent a switch to glycolysis in response to IgG immune complex stimulation, mirroring macrophage metabolic changes in inflamed tissue in vivo. This metabolic reprogramming was required to generate a number of proinflammatory mediators, including IL-1β, and was dependent on mTOR and hypoxia-inducible factor-1α.

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