TY - JOUR
T1 - Maternal immunoglobulin G affects brain development of mouse offspring
AU - Sadakata, Mizuki
AU - Fujii, Kazuki
AU - Kaneko, Ryosuke
AU - Hosoya, Emi
AU - Sugimoto, Hisako
AU - Kawabata-Iwakawa, Reika
AU - Kasamatsu, Tetsuhiro
AU - Hongo, Shoko
AU - Koshidaka, Yumie
AU - Takase, Akinori
AU - Iijima, Takatoshi
AU - Takao, Keizo
AU - Sadakata, Tetsushi
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/12
Y1 - 2024/12
N2 - Maternal immunoglobulin (Ig)G is present in breast milk and has been shown to contribute to the development of the immune system in infants. In contrast, maternal IgG has no known effect on early childhood brain development. We found maternal IgG immunoreactivity in microglia, which are resident macrophages of the central nervous system of the pup brain, peaking at postnatal one week. Strong IgG immunoreactivity was observed in microglia in the corpus callosum and cerebellar white matter. IgG stimulation of primary cultured microglia activated the type I interferon feedback loop by Syk. Analysis of neonatal Fc receptor knockout (FcRn KO) mice that could not take up IgG from their mothers revealed abnormalities in the proliferation and/or survival of microglia, oligodendrocytes, and some types of interneurons. Moreover, FcRn KO mice also exhibited abnormalities in social behavior and lower locomotor activity in their home cages. Thus, changes in the mother-derived IgG levels affect brain development in offsprings.
AB - Maternal immunoglobulin (Ig)G is present in breast milk and has been shown to contribute to the development of the immune system in infants. In contrast, maternal IgG has no known effect on early childhood brain development. We found maternal IgG immunoreactivity in microglia, which are resident macrophages of the central nervous system of the pup brain, peaking at postnatal one week. Strong IgG immunoreactivity was observed in microglia in the corpus callosum and cerebellar white matter. IgG stimulation of primary cultured microglia activated the type I interferon feedback loop by Syk. Analysis of neonatal Fc receptor knockout (FcRn KO) mice that could not take up IgG from their mothers revealed abnormalities in the proliferation and/or survival of microglia, oligodendrocytes, and some types of interneurons. Moreover, FcRn KO mice also exhibited abnormalities in social behavior and lower locomotor activity in their home cages. Thus, changes in the mother-derived IgG levels affect brain development in offsprings.
KW - Brain development
KW - Immunoglobulin G
KW - Microglia
UR - http://www.scopus.com/inward/record.url?scp=85191745783&partnerID=8YFLogxK
U2 - 10.1186/s12974-024-03100-z
DO - 10.1186/s12974-024-03100-z
M3 - 学術論文
C2 - 38698428
AN - SCOPUS:85191745783
SN - 1742-2094
VL - 21
JO - Journal of Neuroinflammation
JF - Journal of Neuroinflammation
IS - 1
M1 - 114
ER -