Macropinocytosis

Macropinocytosis is a form of endocytosis in which cells nonselectively internalize large volumes of extracellular fluid and dissolved molecules, making it important for nutrient uptake, signaling, and disease biology. It begins when actin-driven plasma-membrane ruffles fold back onto the cell surface, enclosing fluid in large vesicles called macropinosomes that mature through the endosomal system and may fuse with lysosomes for degradation. In medicine, macropinocytosis helps explain how immune cells sample their surroundings, how some pathogens enter host cells, and how cancer cells acquire nutrients in nutrient-poor environments. Its pathways are also being investigated for drug and vaccine delivery.

Macropinocytosis - Related Videos

Research

JoVE Journal - Biology
Free Sample

High-throughput Measurement of Dictyostelium discoideum Macropinocytosis by Flow Cytometry

0 Views •

Cited by 8 •

2018

Macropinocytosis, large-scale non-specific fluid uptake, is important in many areas of clinical biology including immunology, infection, cancer, and neurodegenerative diseases. Here, existing techniques have been adapted to allow high-throughput, single-cell resolution measurement of macropinocytosis in the macropinocytosis model organism Dictyostelium discoideum using flow cytometry.

Research

JoVE Journal - Cancer Research

Fluorescence Microscopy for ATP Internalization Mediated by Macropinocytosis in Human Tumor Cells and Tumor-xenografted Mice

0 Views •

Cited by 3 •

2021

We developed a reproducible method to visualize the internalization of nonhydrolyzable fluorescent adenosine triphosphate (ATP), an ATP surrogate, with high cellular resolution. We validated our method using independent in vitro and in vivo assays-human tumor cell lines and immunodeficient mice xenografted with human tumor tissue.

Models and Methods to Evaluate Transport of Drug Delivery Systems Across Cellular Barriers

0 Views •

Cited by 58 •

2013

Many therapeutic applications require safe and efficient transport of drug carriers and their cargoes across cellular barriers in the body. This article describes an adaptation of established methods to evaluate the rate and mechanism of transport of drug nanocarriers (NCs) across cellular barriers, such as the gastrointestinal (GI) epithelium.

Quantification of Membrane Ruffle Formation Using Scanning Electron Microscopy

0 Views •

2025

This video demonstrates sample preparation, fixation, and imaging of a macrophage cell that displays membrane ruffles using scanning electron microscopy, SEM. Detailed information about membrane morphology and organization is crucial for understanding the physiological condition of the cells.

View All Results

FAQs

Related Topics