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Related Concept Videos

Autophagy01:27

Autophagy

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Autophagy is a self-digesting process by which a cell protects itself from threats both within and outside the cell, ranging from abnormal proteins to invading bacteria. In this process, obsolete components of the cell and invading microbes are degraded by hydrolytic enzymes active in an acidic environment of the lysosomal lumen.
An autophagic pathway consists of a series of signaling events activated in response to diverse stress and physiological conditions such as food deprivation,...
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Delivery Pathways to the Lysosome01:36

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Eukaryotic cells use different mechanisms to eliminate toxic waste obsolete and worn-out substances. Lysosomes play a pivotal role in this, and hence, these substances are carried to the lysosome from other parts of the cell and extracellular space through different pathways. The most elaborately studied pathways to the lysosome are the endocytic pathways.
Endocytosis
In endocytosis, the cell membrane takes up macromolecules and particles from the surrounding medium. Clathrin-mediated...
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Cellular Injury V: Apoptosis and Autophagy01:22

Cellular Injury V: Apoptosis and Autophagy

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Cells respond to damage and stress through highly coordinated processes that decide whether they survive or undergo controlled self-destruction. Two major pathways involved in this regulation are apoptosis, a type of programmed cell death, and autophagy, a survival mechanism that helps cells adapt to adverse conditions.ApoptosisApoptosis removes aged or injured cells to maintain tissue balance. During this process, the cell shrinks, chromatin condenses and fragments, and membrane-bound...
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Lysosomal Hydrolases01:22

Lysosomal Hydrolases

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Lysosomes are the site for the degradation of macromolecules and biological polymers released during membrane trafficking events such as secretory, endocytic, autophagic, and phagocytic pathways. The membrane-enclosed area of the lysosome, called the lumen, contains hydrolytic enzymes active in an acidic environment. These acid hydrolases are functional at a pH between 4.5 and 5 and are involved in cellular processes such as cell signaling, energy metabolism, restoration of the plasma membrane,...
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Autophagic Cell Death01:18

Autophagic Cell Death

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Christian de Duve discovered “autophagy,” a process in which cellular components are engulfed by membrane-bound organelles called autophagosomes. The autophagosomes then fuse with lysosomes to digest the enclosed contents. Autophagy is generally activated in cells to prevent cell death. However, cell death is triggered when the damage is beyond repair.
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mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

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The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
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Related Experiment Video

Updated: May 3, 2026

In Situ Immunofluorescent Staining of Autophagy in Muscle Stem Cells
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Autophagy Modulation in Disease Therapy: Where Do We Stand?

Michael P Nelson1, John J Shacka2

  • 1Department of Pathology, Neuropathology Division, University of Alabama at Birmingham, Sparks Clinics Room SC 930B, 1720 7 Ave S., Birmingham, AL 35294, USA.

Current Pathobiology Reports
|January 29, 2014
PubMed
Summary

Autophagy research has advanced, enabling new therapies for diseases like cancer. This review explores current autophagy modulation strategies and drug development for various conditions.

Keywords:
Alzheimer's diseaseParkinson's diseaseautophagycancerdisease treatmentischemianeurodegenerationneuropathologypathobiologypharmacological therapyreperfusionstroke

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Area of Science:

  • Cellular Biology
  • Molecular Biology
  • Pharmacology

Background:

  • Autophagy, a fundamental cellular process, has been studied for over 50 years.
  • Recent advancements have unlocked its therapeutic potential for diverse diseases.
  • The field is rapidly growing, with increasing research and therapeutic applications.

Purpose of the Study:

  • To provide a comprehensive overview of the current landscape of autophagy modulation in disease therapy.
  • To highlight the expanding role of autophagy research in developing targeted therapeutics.
  • To review novel and repurposed drugs being investigated for autophagy-related conditions.

Main Methods:

  • Literature review of recent studies on autophagy and its therapeutic applications.
  • Analysis of emerging treatment strategies involving autophagy modulators.
  • Examination of drug repurposing efforts for autophagy-targeted therapies.

Main Results:

  • Autophagy modulation is a promising therapeutic avenue for various diseases, notably cancer.
  • Established modulators like chloroquine and rapamycin are being creatively applied.
  • Repurposed drugs, such as astemizole, show potential in autophagy-related treatments.
  • The field is dynamic, with ongoing development of novel therapeutic approaches.

Conclusions:

  • Autophagy research has matured, leading to the development of targeted therapeutics.
  • The strategic modulation of autophagy holds significant promise for treating complex diseases.
  • Continued investigation into autophagy mechanisms and drug development is crucial for future therapies.