Molecular Neurobiology

, Volume 41, Issue 2, pp 115–128

Microglia Activation and Anti-inflammatory Regulation in Alzheimer’s Disease

  • Lih-Fen Lue
  • Yu-Min Kuo
  • Thomas Beach
  • Douglas G. Walker

DOI: 10.1007/s12035-010-8106-8

Cite this article as:
Lue, LF., Kuo, YM., Beach, T. et al. Mol Neurobiol (2010) 41: 115. doi:10.1007/s12035-010-8106-8


Inflammatory regulators, including endogenous anti-inflammatory systems, can down-regulate inflammation thus providing negative feedback. Chronic inflammation can result from imbalance between levels of inflammatory mediators and regulators during immune responses. As a consequence, there are heightened inflammatory responses and irreversible tissue damage associated with many age-related chronic diseases. Alzheimer’s disease (AD) brain is marked by prominent inflammatory features, in which microglial activation is the driving force for the elaboration of an inflammatory cascade. How the regulation of inflammation loses its effectiveness during AD pathogenesis remains largely unclear. In this article, we will first review current knowledge of microglial activation and its association with AD pathology. We then discuss four examples of anti-inflammatory systems that could play a role in regulating microglial activation: CD200/CD200 receptor, vitamin D receptor, peroxisome proliferator-activated receptors, and soluble receptor for advanced glycation end products. Through this, we hope to illustrate the diverse aspects of inflammatory regulatory systems in brain and neurodegenerative diseases such as AD. We also propose the importance of neuronal defense systems, because they are part of the integral inflammatory and anti-inflammatory systems. Augmenting the anti-inflammatory defenses of neurons can be included in the strategy for restoration of balanced immune responses during aging and neurodegenerative diseases.


AgingAlzheimer’s diseaseAnti-inflammationCD200CD200 receptorMicroglial activationPeroxisome proliferator-activated receptor γSoluble receptor for advanced glycation end productsVitamin D receptorVitamin D3

Copyright information

© Springer Science+Business Media, LLC 2010

Authors and Affiliations

  • Lih-Fen Lue
    • 1
  • Yu-Min Kuo
    • 2
  • Thomas Beach
    • 3
  • Douglas G. Walker
    • 4
  1. 1.Laboratory of NeuroregenerationBanner Sun Health Research InstituteSun CityUSA
  2. 2.Department of Cell Biology and AnatomyNational Cheng Kung University Medical CollegeTainanTaiwan
  3. 3.Civin Laboratory of NeuropathologySun CityUSA
  4. 4.Laboratory of NeuroinflammationBanner Sun Health Research InstituteSun CityUSA