Phagocytosis executes delayed neuronal death after focal brain ischemia

• Published in: Proceedings of the National Academy of Sciences - PNAS 2013-10, Vol.110 (43), p.E4098-E4107
• Main Authors: Neher, Jonas J, Emmrich, Julius V, Fricker, Michael, Mander, Palwinder K, Théry, Clotilde, Brown, Guy C
• Format: Article
• Language: English
• Subjects: Animals; Antigens, Surface - genetics; Antigens, Surface - metabolism; Atrophy; Biological Sciences; Blotting, Western; Brain; Brain - metabolism; Brain - pathology; Brain Infarction - genetics; Brain Infarction - metabolism; Brain Ischemia - genetics; Brain Ischemia - metabolism; c-Mer Tyrosine Kinase; Cell Death; Cells, Cultured; Dementia; Immunohistochemistry; Inflammation Mediators - metabolism; Ischemia; Macrophages - metabolism; Macrophages - pathology; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Microglia - metabolism; Microglia - pathology; Milk Proteins - genetics; Milk Proteins - metabolism; Neurons; Neurons - metabolism; Neurons - pathology; Phagocytosis; PNAS Plus; Proteins; Proto-Oncogene Proteins - genetics; Proto-Oncogene Proteins - metabolism; Rats; Rats, Mutant Strains; Receptor Protein-Tyrosine Kinases - genetics; Receptor Protein-Tyrosine Kinases - metabolism; Stroke; Time Factors; Up-Regulation
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1308679110

Delayed neuronal loss and brain atrophy after cerebral ischemia contribute to stroke and dementia pathology, but the mechanisms are poorly understood. Phagocytic removal of neurons is generally assumed to be beneficial and to occur only after neuronal death. However, we report herein that inhibition of phagocytosis can prevent delayed loss and death of functional neurons after transient brain ischemia. Two phagocytic proteins, Mer receptor tyrosine kinase (MerTK) and Milk fat globule EGF-like factor 8 (MFG-E8), were transiently up-regulated by macrophages/microglia after focal brain ischemia in vivo. Strikingly, deficiency in either protein completely prevented long-term functional motor deficits after cerebral ischemia and strongly reduced brain atrophy as a result of inhibiting phagocytosis of neurons. Correspondingly, in vitro glutamate-stressed neurons reversibly exposed the “ eat-me ” signal phosphatidylserine, leading to their phagocytosis by microglia; this neuronal loss was prevented in the absence of microglia and reduced if microglia were genetically deficient in MerTK or MFG-E8, both of which mediate phosphatidylserine-recognition. Thus, phagocytosis of viable neurons contributes to brain pathology and, surprisingly, blocking this process is strongly beneficial. Therefore, inhibition of specific phagocytic pathways may present therapeutic targets for preventing delayed neuronal loss after transient cerebral ischemia.