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Infection01:20

Infection

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When a pathogen enters the body and reproduces, it can cause an infection, damage body cells, and cause illness symptoms that eventually lead to disease. Therefore, its prevention requires breaking the chain of infection.
The chain begins with pathogens: bacteria, viruses, fungi, prions, or parasites such as protozoa helminths. These can be present on the skin as transient or resident flora, or they can be acquired from the environment. Identifying and treating the type of infection and...
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Urinary Tract Infection II: Pathophysiology01:25

Urinary Tract Infection II: Pathophysiology

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The pathophysiology of urinary tract infections (UTIs) encompasses several progressive stages, beginning with bacterial colonization and culminating in potential systemic complications if untreated. UTIs are primarily initiated by bacteria, such as Escherichia coli, which often originate from the gastrointestinal tract and migrate to the urinary system through the periurethral area. This migration can occur via several routes, including improper hygiene practices, sexual activity, or...
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Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

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Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
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Pneumonia II: Pathophysiology01:29

Pneumonia II: Pathophysiology

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The pathophysiology of pneumonia involves the following steps:
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Stages of Infection01:26

Stages of Infection

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Stages of infection describe what happens to a susceptible host once a pathogen invades the human body. The stages of infection are incubation, prodromal, illness, stage of decline, and convalescence. The incubation stage is the period from exposure to a pathogen until symptoms start. The infected person is unaware of impending illness as the pathogens grow and multiply within the body. The duration may vary depending on the type of infection. The incubation period of measles averages ten to...
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Defense Against Bacterial Pathogens01:31

Defense Against Bacterial Pathogens

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The human immune system is a complex network of cells, tissues, and organs that work together to defend the body against bacterial infections. It consists of various immune cells, each playing a specific role in the defense mechanism.
Phagocytes
Phagocytes are the frontline soldiers of the immune system. They include neutrophils and macrophages. Neutrophils are the most abundant type of white blood cell and are quickly mobilized to the site of infection. Macrophages are larger cells that patrol...
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Video Experimental Relacionado

Updated: Jan 7, 2026

Mouse Footpad Inoculation Model to Study Viral-Induced Neuroinflammatory Responses
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Mouse Footpad Inoculation Model to Study Viral-Induced Neuroinflammatory Responses

Published on: June 14, 2020

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Ciencia básica y patogénesis

Han Zhao1, Haowei Xu2, Junkai Xie1

  • 1Purdue University, West Lafayette, IN, USA.

Alzheimer's & dementia : the journal of the Alzheimer's Association
|December 24, 2025
PubMed
Resumen
Este resumen es generado por máquina.

Los investigadores desarrollaron un nuevo biosensor FRET para rastrear la agregación de TDP-43 en neuronas vivas, un factor clave en la enfermedad de Alzheimer y demencias relacionadas (ADRD). Esta herramienta ayuda a comprender la progresión de la enfermedad e identificar objetivos terapéuticos para la ADRD.

Palabras clave:
biosensor FRETTDP-43agregación de proteínasneuronasenfermedad de Alzheimerdemencias relacionadas con el Alzheimerneurocienciabiología molecularbioquímica

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Área de la Ciencia:

  • Neurociencia
  • Biología Molecular
  • Bioquímica

Sus antecedentes:

  • La enfermedad de Alzheimer y las demencias relacionadas (ADRD) afectan a millones de personas, y la patología de TDP-43 se relaciona cada vez más con el deterioro cognitivo.
  • Los mecanismos moleculares del papel de TDP-43 en la ADRD se comprenden mal debido a la falta de herramientas para monitorizar su agregación en células vivas.

Objetivo del estudio:

  • Ingenierizar un biosensor basado en la transferencia de energía por resonancia de Förster (FRET) para detectar la agregación de TDP-43 en tiempo real dentro de neuronas vivas.
  • Utilizar este biosensor para investigar la progresión de la patología de TDP-43 en condiciones que imitan el estrés celular relacionado con el envejecimiento.

Principales métodos:

  • Se diseñó un biosensor FRET utilizando varios isoformas de TDP-43 y construcciones de enlace.
  • Se validó la sensibilidad del biosensor utilizando condiciones de estrés de proteostasis y fibrillas de TDP-43 preformadas.
  • Se transpuso el biosensor a neuronas corticales derivadas de iPSC humanas y se monitorizaron los cambios en la señal FRET después del tratamiento con estresores que imitan el envejecimiento.

Principales resultados:

  • El biosensor FRET detectó con éxito la agregación de TDP-43 en respuesta a estresores de proteostasis.
  • Las neuronas tratadas con compuestos que imitan el envejecimiento mostraron un aumento de las señales FRET, lo que indica una agregación progresiva de TDP-43 con el tiempo.

Conclusiones:

  • Se desarrolló un nuevo biosensor FRET para la monitorización en tiempo real de la agregación de TDP-43 en neuronas vivas.
  • Esta herramienta facilita el estudio de la dinámica de la patología de TDP-43 y la identificación de vías moleculares alteradas en la ADRD.