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Microglia and Astrocytes in Disease: Dynamic Duo or Partners in Crime?

Journal

TRENDS IN IMMUNOLOGY
Volume 41, Issue 9, Pages 820-835

Publisher

CELL PRESS
DOI: 10.1016/j.it.2020.07.006

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Categories

Funding

  1. National Institute on Aging [P30AG10161, R01AG15819, R01AG17917, R01AG30146, R01AG36836, U01AG32984, U01AG46152]
  2. Illinois Department of Public Health
  3. Translational Genomics Research Institute
  4. University of California, Irvine Startup funds
  5. American Federation of Aging Research
  6. Cure Alzheimer's Fund

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Microglia-astrocyte interactions represent a delicate balance affecting neural cell functions in health and disease. Tightly controlled to maintain homeostasis during physiological conditions, rapid and prolonged departures during disease, infection, and following trauma drive multiple outcomes: both beneficial and detrimental. Recent sequencing studies at the bulk and single-cell level in humans and rodents provide new insight into microglia-astrocyte communication in homeostasis and disease. However, the complex changing ways these two cell types functionally interact has been a barrier to understanding disease initiation, progression, and disease mechanisms. Single cell sequencing is providing new insights; however, many questions remain. Here, we discuss how to bridge transcriptional states to specific functions so we can develop therapies to mediate negative effects of altered microglia-astrocyte interactions.

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