Distinct Physiologic Properties of Microglia and Blood-Borne Cells in Rat Brain Slices After Permanent Middle Cerebral Artery Occlusion

• Published in: Journal of cerebral blood flow and metabolism 2000-11, Vol.20 (11), p.1537-1549
• Main Authors: Lyons, Susan A., Pastor, Andrea, Ohlemeyer, Carsten, Kann, Oliver, Wiegand, Frank, Prass, Konstantin, Knapp, Felix, Kettenmann, Helmut, Dirnagl, Ulrich
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Brain Ischemia - immunology; Brain Ischemia - metabolism; Brain Ischemia - physiopathology; Cell Movement - immunology; Cerebral Cortex - blood supply; Cerebral Cortex - cytology; Cerebral Cortex - physiology; Immunophenotyping; Infarction, Middle Cerebral Artery - immunology; Infarction, Middle Cerebral Artery - metabolism; Infarction, Middle Cerebral Artery - physiopathology; Leukocytes - chemistry; Leukocytes - cytology; Leukocytes - immunology; Male; Medical sciences; Membrane Potentials - immunology; Microglia - chemistry; Microglia - cytology; Microglia - physiology; Microscopy, Video; Neurology; Organ Culture Techniques; Patch-Clamp Techniques; Potassium - physiology; Potassium Channels - analysis; Potassium Channels - metabolism; Rats; Rats, Wistar; Vascular diseases and vascular malformations of the nervous system
• ISSN: 0271-678X; 1559-7016
• DOI: 10.1097/00004647-200011000-00003

The authors investigated the time course of leukocyte infiltration compared with microglial activation in adult rat brain slices after permanent middle cerebral artery occlusion (MCAO). To distinguish peripheral leukocytes from microglia, the blood cells were prelabeled in vivo with Rhodamine 6G (Rhod6G) IV before induction of ischemia. At specific times after infarct, invading leukocytes, microglia, and endothelial cells were labeled in situ with isolectin (IL)B4-FITC (ILB4). Six hours after MCAO only a few of the ILB4+ cells were colabeled by Rhod6G. These cells expressed the voltage-gated inwardly and outwardly rectifying K+ currents characteristic of macrophages. The majority of the ILB4+ cells were Rhod6G− and expressed a lack of voltage-gated channels, recently described for ramified microglial cells in brain slices, or exhibited only an inward rectifier current, a unique marker for cultured (but unstimulated) microglia. Forty-eight hours after MCAO, all blood-borne and the majority of Rhod6G− cells expressed outward and inward currents indicating that the intrinsic microglial population exhibited physiologic features of stimulated, cultured microglia. The ILB4+/Rhod6G− intrinsic microglial population was more abundant in the border zone of the infarct and their morphology changed from radial to ameboid. Within this zone, the authors observed rapidly migrating cells and recorded this movement by time-lapse microscopy. The current findings indicate that microglial cells acquire physiologic features of leukocytes at a later time point after MCAO.