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Cross-bridge Cycle01:26

Cross-bridge Cycle

As muscle contracts, the overlap between the thin and thick filaments increases, decreasing the length of the sarcomere—the contractile unit of the muscle—using energy in the form of ATP. At the molecular level, this is a cyclic, multistep process that involves binding and hydrolysis of ATP, and movement of actin by myosin.
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Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds the telomeric...
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The Effect of Aging on Tissues

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Related Experiment Video

Updated: Jun 21, 2026

Preparation and Culture of Myogenic Precursor Cells/Primary Myoblasts from Skeletal Muscle of Adult and Aged Humans
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Centrosome misorientation reduces stem cell division during ageing.

Jun Cheng1, Nezaket Türkel, Nahid Hemati

  • 1Department of Biomedical Engineering, Center for Ultrafast Optical Science, University of Michigan, Ann Arbor, Michigan 48109, USA.

Nature
|October 17, 2008
PubMed
Summary

Stem cell aging in Drosophila is linked to misoriented centrosomes, disrupting asymmetric division and leading to reduced sperm production. Correcting orientation allows stem cells to re-enter the cell cycle.

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Area of Science:

  • Developmental Biology
  • Cell Biology
  • Aging Research

Background:

  • Adult stem cells maintain tissue homeostasis through asymmetric division.
  • Stem cell function decline contributes to tissue aging, but mechanisms are unclear.
  • Spermatogenesis decline in aged Drosophila males suggests stem cell dysfunction.

Purpose of the Study:

  • Investigate the mechanism linking stem cell aging to reduced spermatogenesis in Drosophila.
  • Determine the role of stem cell orientation and centrosome positioning in aging.

Main Methods:

  • Microscopy to observe centrosome orientation in Drosophila germline stem cells (GSCs).
  • Analysis of cell cycle progression in GSCs with varying centrosome orientation.
  • Tracking GSCs and spermatogonia to identify origins of misoriented cells.

Main Results:

  • Aging Drosophila GSCs accumulate with misoriented centrosomes.
  • Misoriented GSCs exhibit cell cycle arrest or delay.
  • Transient cell cycle arrest is resolved upon correction of centrosome orientation.
  • Some misoriented GSCs may arise from dedifferentiation of spermatogonia.

Conclusions:

  • Centrosome misorientation in aging GSCs disrupts asymmetric division and contributes to spermatogenesis decline.
  • Cell cycle arrest linked to misorientation acts as a safeguard for asymmetric division.
  • Maintaining correct stem cell orientation is crucial for tissue homeostasis during aging.