Comparative distribution of tau phosphorylated at Ser262 in pre-tangles and tangles

Neurobiol Aging. 2003 Oct;24(6):767-76. doi: 10.1016/s0197-4580(02)00228-2.

Abstract

The Phospho-Ser(262) epitope of phosphorylated tau, which accumulates in tangles in Alzheimer's disease (AD) brains, has been shown to have a strong disruptive effect on microtubules. Using antibodies which specifically recognize the Phospho-Ser(262) of tau, we compared the presence of this epitope in normal appearing neurons (pre-tangles) and tangles, with the presence of Phospho-Ser(199/202) (AT-8) and Phospho-Ser(396/404) (PHF-1) epitopes. All antibodies visualized lightly or darkly stained pre-tangles, neurons with immunoreactive clumps, intracellular and extracellular tangles. Pre-tangles were more abundant in control cases which showed some pathology, when compared with AD brains. Immunoreactivity for Phospho-Ser(262) was preferentially present in intracellular and extracellular tangles and was found in a significantly smaller number of pre-tangles when compared with the other epitopes. These results indicate the presence of various epitopes of Phospho-Tau in a substantial number of pre-tangles which may represent an early marker of tangle formation. The differential distribution of various epitopes suggests that the presence of the Phospho-Ser(262) epitope of tau either accelerates the transition form pre-tangle to tangle, or appears later than the other epitopes in the process of tangle formation.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / pathology
  • Alzheimer Disease / physiopathology*
  • Cerebral Cortex / physiopathology*
  • Epitopes / metabolism
  • Humans
  • Immunohistochemistry
  • Middle Aged
  • Neurofibrillary Tangles / classification
  • Neurofibrillary Tangles / metabolism*
  • Neurons / metabolism*
  • Neurons / pathology
  • Phosphorylation
  • Serine / metabolism
  • Tissue Distribution
  • tau Proteins / metabolism*

Substances

  • Epitopes
  • tau Proteins
  • Serine