Medical Hypotheses
Volume 52, Issue 6 , Pages 525-527, June 1999

Re-entry into the cell cycle: a mechanism for neurodegeneration in Alzheimer disease

  • A. McShea

      Affiliations

    • Bristol-Myers Squibb, Pharmaceutical Research Institute, Seattle, Washington, DC, U.S.A.
  • ,
  • A.F. Wahl

      Affiliations

    • Bristol-Myers Squibb, Pharmaceutical Research Institute, Seattle, Washington, DC, U.S.A.
  • ,
  • M.A. Smith

      Affiliations

    • Institute of Pathology, Case Western Reserve University, Cleveland, OH, U.S.A.

Received 24 July 1997; accepted 15 October 1997.

Abstract 

Several recent findings demonstrated increased expression of cell cycle-related proteins in the degenerating neurons found in Alzheimer disease. We hypothesize that this apparent attempt to re-enter the cell cycle is a neuronal response to external growth stimuli that leads to an abortive re-entry into the cell cycle. However, since neurons of adults apparently lack the capacity both to divide in vivo and in vitro, it is possible that they lack the components necessary to complete the cell division process. Nonetheless, the importance of these findings is that they provide an explanation for the increased phosphorylation of cytoskeletal proteins such as τ and neurofilaments that represent the most striking intracellular changes in the disease. Further, it is our contention that inappropriate re-entry into the cell cycle and interrupted mitotic processes are significant factors not only in the cytoskeletal pathology but also in the neuronal degeneration that characterizes the pathology of Alzheimer disease.

No full text is available. To read the body of this article, please view the PDF online.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0306-9877(97)90680-0

doi:10.1054/mehy.1997.0680

Medical Hypotheses
Volume 52, Issue 6 , Pages 525-527, June 1999