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Related Concept Videos

Cellular Injury V: Apoptosis and Autophagy01:22

Cellular Injury V: Apoptosis and Autophagy

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...
Apoptosis01:30

Apoptosis

Apoptosis is a combination of two Greek words, 'apo' and 'ptosis,' meaning separation and falling off, respectively. Hippocrates used this word to describe gangrene, which was caused due to bandaging of fractured bones. Apoptosis was distinguished from necrosis in 1970 when John Kerr reported observations of morphological changes occurring during apoptosis. During one experiment, he observed that the disruption of blood supply to the liver tissue resulted in a size reduction of the tissue.
The Intrinsic Apoptotic Pathway01:31

The Intrinsic Apoptotic Pathway

Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
The Extrinsic Apoptotic Pathway01:17

The Extrinsic Apoptotic Pathway

The extrinsic apoptotic pathway is initiated when extracellular death-inducing signals, such as specific cytokines, activate the death receptors expressed on the cell surface. The immune cells involved in this pathway are natural killer cells (NK cells) and cytotoxic T-lymphocytes. NK cells are critical in innate immune response, while cytotoxic T-lymphocytes are associated with adaptive immune response. These cells recognize specific receptors expressed on the altered cells and activate...
Autophagic Cell Death01:18

Autophagic Cell Death

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.
Autophagy and Apoptosis
Autophagy can activate apoptosis. In normal conditions, the autophagy activating protein Beclin-1 and pro-apoptotic...
Overview of Cell Death01:30

Overview of Cell Death

Cell death is an essential process where the body gets rid of old or damaged cells. Cell proliferation and death need to be balanced, as an imbalance between the two may lead to cancer or autoimmune diseases.
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the 20th century...

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Related Experiment Video

Updated: Jun 20, 2026

Activation of Apoptosis by Cytoplasmic Microinjection of Cytochrome c
07:42

Activation of Apoptosis by Cytoplasmic Microinjection of Cytochrome c

Published on: June 29, 2011

Coupling cellular mitogenesis to apoptosis by designed biomolecules.

Qiong Lin1, Fengchang Zhu, Wannian Yang

  • 1Weis Center for Research, Geisinger Clinic, Danville, PA 17822, United States.

Cellular Signalling
|September 17, 2009
PubMed
Summary
This summary is machine-generated.

Researchers engineered a molecular device (MCAMD) to link cancer cell growth signals directly to cell death pathways. This novel approach shows promise for developing new cancer gene therapies by targeting constitutively active mitogenesis.

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Area of Science:

  • Molecular Biology
  • Cell Signaling
  • Biotechnology

Background:

  • Cellular signal transduction pathways are crucial for regulating cell responses to external stimuli.
  • Aberrant signaling, particularly constitutive mitogenesis in cancer, drives uncontrolled cell proliferation.
  • Targeting these pathways offers potential therapeutic strategies for cancer treatment.

Purpose of the Study:

  • To engineer a novel molecular system that couples mitogenic (growth-promoting) signals to apoptotic (programmed cell death) outputs.
  • To investigate the feasibility of manipulating cellular signaling to induce cancer cell death.

Main Methods:

  • Reconstruction of key components from both mitogenic (Ras, Raf) and apoptotic (caspase-3) signaling pathways.
  • Integration of these components to create a synthetic biological circuit.

Main Results:

  • Successfully engineered a molecular device, termed "mitogenesis coupled-apoptosis molecular device" (MCAMD).
  • Demonstrated the ability of MCAMD to couple mitogenic signal input to apoptotic output in cells.
  • MCAMD effectively links growth signals to cell death machinery.

Conclusions:

  • MCAMD represents a novel biomolecular tool for redirecting cellular signaling.
  • The constitutive activation of mitogenesis in cancer cells makes MCAMD a potential candidate for cancer gene therapy applications.
  • This synthetic biology approach offers a new avenue for cancer treatment development.