TY - JOUR
T1 - Origin and Emergence of Microglia in the CNS—An Interesting (Hi)story of an Eccentric Cell
AU - Dermitzakis, Iasonas
AU - Manthou, Maria Eleni
AU - Meditskou, Soultana
AU - Tremblay, Marie Ève
AU - Petratos, Steven
AU - Zoupi, Lida
AU - Boziki, Marina
AU - Kesidou, Evangelia
AU - Simeonidou, Constantina
AU - Theotokis, Paschalis
N1 - Publisher Copyright:
© 2023 by the authors.
PY - 2023/3
Y1 - 2023/3
N2 - Microglia belong to tissue-resident macrophages of the central nervous system (CNS), representing the primary innate immune cells. This cell type constitutes ~7% of non-neuronal cells in the mammalian brain and has a variety of biological roles integral to homeostasis and pathophysiology from the late embryonic to adult brain. Its unique identity that distinguishes its “glial” features from tissue-resident macrophages resides in the fact that once entering the CNS, it is perennially exposed to a unique environment following the formation of the blood–brain barrier. Additionally, tissue-resident macrophage progenies derive from various peripheral sites that exhibit hematopoietic potential, and this has resulted in interpretation issues surrounding their origin. Intensive research endeavors have intended to track microglial progenitors during development and disease. The current review provides a corpus of recent evidence in an attempt to disentangle the birthplace of microglia from the progenitor state and underlies the molecular elements that drive microgliogenesis. Furthermore, it caters towards tracking the lineage spatiotemporally during embryonic development and outlining microglial repopulation in the mature CNS. This collection of data can potentially shed light on the therapeutic potential of microglia for CNS perturbations across various levels of severity.
AB - Microglia belong to tissue-resident macrophages of the central nervous system (CNS), representing the primary innate immune cells. This cell type constitutes ~7% of non-neuronal cells in the mammalian brain and has a variety of biological roles integral to homeostasis and pathophysiology from the late embryonic to adult brain. Its unique identity that distinguishes its “glial” features from tissue-resident macrophages resides in the fact that once entering the CNS, it is perennially exposed to a unique environment following the formation of the blood–brain barrier. Additionally, tissue-resident macrophage progenies derive from various peripheral sites that exhibit hematopoietic potential, and this has resulted in interpretation issues surrounding their origin. Intensive research endeavors have intended to track microglial progenitors during development and disease. The current review provides a corpus of recent evidence in an attempt to disentangle the birthplace of microglia from the progenitor state and underlies the molecular elements that drive microgliogenesis. Furthermore, it caters towards tracking the lineage spatiotemporally during embryonic development and outlining microglial repopulation in the mature CNS. This collection of data can potentially shed light on the therapeutic potential of microglia for CNS perturbations across various levels of severity.
KW - development
KW - microglia
KW - molecular cues
KW - origin
KW - progeny
KW - yolk sac
UR - https://www.scopus.com/pages/publications/85151146844
U2 - 10.3390/cimb45030171
DO - 10.3390/cimb45030171
M3 - Review Article
C2 - 36975541
AN - SCOPUS:85151146844
SN - 1467-3037
VL - 45
SP - 2609
EP - 2628
JO - Current Issues in Molecular Biology
JF - Current Issues in Molecular Biology
IS - 3
ER -