Video Experimental Relacionado
Updated: Sep 28, 2026

16:01
Investigating Mast Cell Secretory Granules; from Biosynthesis to Exocytosis
Published on: January 26, 2015
Exposición de un antígeno de gránulos de cromafina en la superficie celular durante la exocitosis
Nature
|February 17, 1983
Resumen
Las membranas de gránulos de cromafina se recuperan y se reutilizan para la secreción. Este estudio cuantifica la eliminación de la membrana de la superficie celular después de la exocitosis, mostrando una desaparición significativa en 30 minutos.
Área de la Ciencia:
- Biología celular Biología celular.
- La neurociencia es la neurociencia.
- El tráfico de membranas.
Sus antecedentes:
- La tasa de síntesis de las proteínas de membrana en las vesículas de almacenamiento de catecolaminas (gránulos de cromafina) es menor que la de las proteínas secretoras.
- Esto sugiere que las membranas de gránulos de cromafina se recuperan y reutilizan para múltiples ciclos de secreción después de la exocitosis.
- Estudios previos mostraron la absorción de marcadores exógenos en los orgánulos de Golgi y inmaduros, apoyando la reutilización de la membrana.
Objetivo del estudio:
- Investigar si las membranas secretoras de los orgánulos se eliminan específica y completamente de la membrana plasmática después de la exocitosis.
- Para determinar la velocidad a la que se produce este proceso de eliminación de la membrana.
Principales métodos:
- Utilizando un antisuero contra una glicoproteína de membrana específica que se encuentra en los gránulos de cromafina.
- Analizar cuantitativamente la exposición y la posterior desaparición de este antígeno en la superficie celular después de la exocitosis.
Principales resultados:
- El antígeno glicoproteínico de membrana de los gránulos de cromafina queda expuesto en la superficie celular durante la exocitosis.
- Los datos cuantitativos muestran que este antígeno desaparece en gran medida de la superficie celular en 30 minutos.
Conclusiones:
- De hecho, las membranas de gránulos de cromafina se eliminan de la membrana plasmática después de la exocitosis.
- El proceso de eliminación es relativamente rápido, con una porción significativa de los componentes de la membrana desapareciendo en 30 minutos, apoyando el concepto de recuperación y reutilización de la membrana.
Videos de Conceptos Relacionados
Exocytosis
Exocytosis is used to release material from cells. Like other bulk transport mechanisms, exocytosis requires energy.
Exocytosis
Exocytosis is a process that releases molecules outside the cell. Like other bulk transport mechanisms, exocytosis requires energy.
Exocytosis is the opposite of endocytosis, which brings molecules inside the cell. Sometimes, the released materials are signaling molecules. For example, neurons typically use exocytosis to release neurotransmitters. Cells also use exocytosis to insert proteins such as ion channels into their cell membranes, secrete proteins for use in the extracellular matrix, or...
Exocytosis is the opposite of endocytosis, which brings molecules inside the cell. Sometimes, the released materials are signaling molecules. For example, neurons typically use exocytosis to release neurotransmitters. Cells also use exocytosis to insert proteins such as ion channels into their cell membranes, secrete proteins for use in the extracellular matrix, or...
Overview of Secretory Vesicles
Secretory vesicles, also known as dense core vesicles (DCVs), are membrane-bound vesicles that transport secretory proteins, such as hormones or neurotransmitters. Regulated secretory vesicles transport proteins from the trans-Golgi network to the exterior of the cell. Proteins present in regulated secretory vesicles are required to be rapidly exocytosed in large amounts upon a specific stimulus.
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
Fusion of Secretory Vesicles with the Plasma Membrane
Proteins and neurotransmitters in secretory vesicles can be released from a cell upon vesicle docking, priming, and fusion with the plasma membrane. Vesicles are docked and primed in preparation for the quick exocytosis of their contents in response to a stimulus. The fusion process is mainly carried out by a SNAP Receptor or SNARE complex, consisting of synaptobrevin, syntaxin-1, and SNAP-25.
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
Insulin Secretory Vesicles
Insulin secretory vesicles release insulin to stimulate blood glucose uptake and regulate carbohydrate metabolism. When the blood glucose levels increase, glucose enters the pancreatic β-islet cells through glucose transporters. Once inside, glucose is metabolized through glycolysis, the citric acid cycle, and the electron transport chain, producing ATP. This increase in ATP concentration closes ATP-sensitive potassium channels, leading to depolarization of the membrane and the opening of...
Vesicular Trasport: Endocytosis, Transcytosis and Exocytosis
Vesicular transport is a cellular process that encompasses the engulfment of particles or dissolved substances by cells. It involves endocytosis, transcytosis, and exocytosis.
Endocytosis is a cellular mechanism that involves the inward folding of the cell membrane to create vesicles that capture and transport large drug molecules. This process comprises two distinct methods: pinocytosis (often referred to as "cell drinking") and phagocytosis (often referred to as "cell eating"). Pinocytosis is...
Endocytosis is a cellular mechanism that involves the inward folding of the cell membrane to create vesicles that capture and transport large drug molecules. This process comprises two distinct methods: pinocytosis (often referred to as "cell drinking") and phagocytosis (often referred to as "cell eating"). Pinocytosis is...

