AI Article Synopsis

  • - The study explores how brain injuries trigger specific responses in cells, indicating that there's a system in place to communicate injury details at the molecular level, though the exact mechanisms aren't fully understood.
  • - Researchers discovered a phenomenon called Inflares, which are bursts of ATP released from astrocytes (a type of brain cell) that signal injury characteristics like intensity and location.
  • - The findings suggest that when there's a mismatch in the injury signals (Inflares) and actual injury severity, it can lead to problems with microglia (immune cells in the brain), worsening recovery; blocking Inflares in stroke models helps reduce damage and improve healing.

Article Abstract

Injuries to the brain result in tunable cell responses paired with stimulus properties, suggesting the existence of intrinsic processes that encode and transmit injury information; however, the molecular mechanism of injury information encoding is unclear. Here, using ATP fluorescent indicators, we identify injury-evoked spatiotemporally selective ATP dynamics, Inflares, in adult mice of both sexes. Inflares are actively released from astrocytes and act as the internal representations of injury. Inflares encode injury intensity and position at their population level through frequency changes and are further decoded by microglia, driving changes in their activation state. Mismatches between Inflares and injury severity lead to microglia dysfunction and worsening of injury outcome. Blocking Inflares in ischemic stroke in mice reduces secondary damage and improves recovery of function. Our results suggest that astrocytic ATP dynamics encode injury information and are sensed by microglia.

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Source
http://dx.doi.org/10.1038/s41593-024-01680-wDOI Listing

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