Secreted APP regulates the function of full-length APP in neurite outgrowth through interaction with integrin beta1
2008

How APP and its secreted form affect nerve growth

publication 10 minutes Evidence: moderate

Author Information

Author(s): Young-Pearse Tracy L, Chen Allen C, Chang Rui, Marquez Cesar, Selkoe Dennis J

Primary Institution: Center for Neurologic Diseases, Brigham and Women's Hospital and Harvard Medical School

Hypothesis

APPs-α may act to oppose effects of cell-surface APP and its homologues by competitively binding to factors that normally interact with the holoprotein to inhibit neurite outgrowth.

Conclusion

APPs-α regulates the function of APP in neurite outgrowth via the novel mechanism of competing with the binding of APP to Itgβ1.

Supporting Evidence

  • Neurons lacking APP showed longer neurite lengths, indicating APP's role in regulating neurite outgrowth.
  • APPs-α application promoted neurite outgrowth in wild-type neurons but had no effect in APP knock-out neurons.
  • Blocking Integrin β1 inhibited the neurite outgrowth effects of both APP deletion and APPs-α application.

Takeaway

This study shows that a protein called APP helps nerve cells grow, and its secreted form, APPs-α, can actually stop it from working too much.

Methodology

The study involved culturing primary neurons from APP knock-out and wild-type mice and measuring neurite lengths after treatment with APPs-α.

Limitations

The study primarily focuses on in vitro results, which may not fully represent in vivo conditions.

Participant Demographics

Neurons from embryonic day 18 (E18) mice were used.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1749-8104-3-15

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