Microglial repopulation model reveals a robust homeostatic process for replacing CNS myeloid cells

Proceedings of the National Academy of Sciences of the United States of America

Volumn 109, Issue 44, 2012, Pages 18150-18155

  Varvel, Nicholas H ^a   Grathwohl, Stefan A ^a   Baumann, Frank ^a   Liebig, Christian ^a   Bosch, Andrea ^a   Brawek, Bianca ^b   Thal, Dietmar R ^c   Charo, Israel F ^d   Heppner, Frank L ^e   Aguzzi, Adriano ^f   Garaschuk, Olga ^b   Ransohoff, Richard M ^g   Jucker, Mathias ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b UNIVERSITY OF TÜBINGEN   (Germany)

^c UNIVERSITY OF ULM   (Germany)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^f UNIVERSITY HOSPITAL ZURICH   (Switzerland)

^g LERNER RESEARCH INSTITUTE   (United States)

Author keywords

Chemokines; In vivo calcium imaging; Myeloid cell heterogeneity; Neuroinflammation

Indexed keywords

CD45 ANTIGEN; CHEMOKINE RECEPTOR CCR2;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; BLOOD VESSEL; BONE MARROW CELL; BRAIN REGION; CALCIUM CELL LEVEL; CELL DEATH; CELL STRUCTURE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; ENGRAFTMENT; FEMALE; HOMEOSTASIS; MALE; MICROGLIA; MOUSE; NONHUMAN; PRIORITY JOURNAL;

ADENOSINE TRIPHOSPHATE; ANIMALS; CENTRAL NERVOUS SYSTEM; HOMEOSTASIS; MICE; MICROGLIA; THYMIDINE KINASE;

MUS MUSCULUS;

EID: 84868092714     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1210150109     Document Type: Article

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