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Mitogens and the Cell Cycle02:38

Mitogens and the Cell Cycle

Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
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Cell size is a significant factor impacting cellular design, function, and fitness. There exists some internal coordination by which cells double their masses before division, thus, achieving homeostasis. Coordination between cell growth and proliferation depends on the checkpoints in between cell cycle phases. Loss of coordination or failure in the checkpoint mechanism can drive the cell to uncontrolled growth and loss of cellular function. Like dividing cells that coordinate cellular growth,...
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Regulation of Hematopoietic Stem Cells

All blood and immune cells are produced from the multipotent hematopoietic stem cells (HSCs) by the process of hematopoiesis. However, they all have a limited life span. In addition, many are depleted in immune surveillance or combatting an injury or infection. This makes blood one of the most regenerative tissues. Hematopoiesis helps replenish these blood and immune cells, restoring the body's normal functioning. However, overproduction of blood and immune cells can make them cancerous or...
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TGF - β Signaling Pathway

The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors are of three kinds RI, RII, and RIII. The RI...
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Related Experiment Video

Updated: Jun 10, 2026

Inducing Dendritic Growth in Cultured Sympathetic Neurons
09:52

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Published on: March 21, 2012

Schwann cell growth factors.

M C Raff, E Abney, J P Brockes

    Cell
    |November 1, 1978
    PubMed
    Summary

    Bovine pituitary and brain extracts significantly stimulate rat Schwann cell proliferation, independent of cyclic AMP levels. This suggests at least two distinct pathways regulate Schwann cell division.

    Area of Science:

    • Neuroscience
    • Cell Biology
    • Biochemistry

    Background:

    • Schwann cells are crucial for peripheral nerve function.
    • Understanding Schwann cell proliferation is key for nerve regeneration research.
    • Existing growth factors do not fully explain Schwann cell mitogenesis.

    Purpose of the Study:

    • To identify factors that promote Schwann cell proliferation.
    • To investigate the mechanisms underlying Schwann cell growth stimulation.
    • To explore potential synergistic effects with known mitogens.

    Main Methods:

    • Culturing purified rat Schwann cells.
    • Testing crude bovine tissue extracts (pituitary, brain, nerve roots, liver, kidney) for mitogenic activity.
    • Assessing the effect of fetal calf serum (FCS) and various hormones.

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  • Investigating the role of cyclic AMP (cAMP) and cholera toxin.
  • Main Results:

    • Crude pituitary and brain extracts markedly enhanced Schwann cell proliferation.
    • Pituitary extracts were more potent mitogens than brain extracts.
    • Neither pituitary nor brain extracts increased cAMP levels, but they synergized with cholera toxin.
    • FCS was required but insufficient alone for optimal proliferation.

    Conclusions:

    • Bovine pituitary and brain contain potent, heat-labile mitogens for Schwann cells.
    • At least two distinct signaling pathways stimulate Schwann cell division.
    • One pathway involves increased intracellular cAMP, while another does not.