Emerging roles for ITAM and ITIM receptor signaling in microglial biology and Alzheimer's disease‐related amyloidosis

Author:

Samuels Joshua D.123,Lukens John R.12ORCID,Price Richard J.23

Affiliation:

1. Department of Neuroscience, Center for Brain Immunology and Glia (BIG) University of Virginia (UVA) Charlottesville Virginia USA

2. Neuroscience Graduate Program University of Virginia Charlottesville Virginia USA

3. Department of Biomedical Engineering University of Virginia Charlottesville Virginia USA

Abstract

AbstractMicroglia are critical responders to amyloid beta (Aβ) plaques in Alzheimer's disease (AD). Therefore, the therapeutic targeting of microglia in AD is of high clinical interest. While previous investigation has focused on the innate immune receptors governing microglial functions in response to Aβ plaques, how microglial innate immune responses are regulated is not well understood. Interestingly, many of these microglial innate immune receptors contain unique cytoplasmic motifs, termed immunoreceptor tyrosine‐based activating and inhibitory motifs (ITAM/ITIM), that are commonly known to regulate immune activation and inhibition in the periphery. In this review, we summarize the diverse functions employed by microglia in response to Aβ plaques and also discuss the innate immune receptors and intracellular signaling players that guide these functions. Specifically, we focus on the role of ITAM and ITIM signaling cascades in regulating microglia innate immune responses. A better understanding of how microglial innate immune responses are regulated in AD may provide novel therapeutic avenues to tune the microglial innate immune response in AD pathology.image

Funder

National Institute of Neurological Disorders and Stroke

National Institute of Biomedical Imaging and Bioengineering

Brain Institute, University of Virginia

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

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