TY - JOUR
T1 - Pathogenesis of Germinal Matrix Hemorrhage
T2 - Insights from Single-Cell Transcriptomics
AU - Chen, Jiapei
AU - Choi, Jennifer Ja Yoon
AU - Lin, Pin Yeh
AU - Huang, Eric J.
N1 - Publisher Copyright:
© 2025 Annual Reviews Inc.. All rights reserved.
PY - 2025/1/24
Y1 - 2025/1/24
N2 - The germinal matrix harbors neurogenic niches in the subpallium of the prenatal human brain that produce abundant GABAergic neurons. In preterm infants, the germinal matrix is particularly vulnerable to developing hemorrhage, which disrupts neurogenesis and causes severe neurodevelopmental sequelae. However, the disease mechanisms that promote germinal matrix hemorrhage remain unclear. Here, we review recent advances using single-cell transcriptomics to uncover novel mechanisms that govern neurogenesis and angiogenesis in the germinal matrix of the prenatal human brain. These approaches also reveal the critical role of immune–vascular interaction that promotes vascular morphogenesis in the germinal matrix and how proinflammatory factors from activated neutrophils and monocytes can disrupt this process, leading to hemorrhage. Collectively, these results reveal fundamental disease mechanisms and therapeutic interventions for germinal matrix hemorrhage.
AB - The germinal matrix harbors neurogenic niches in the subpallium of the prenatal human brain that produce abundant GABAergic neurons. In preterm infants, the germinal matrix is particularly vulnerable to developing hemorrhage, which disrupts neurogenesis and causes severe neurodevelopmental sequelae. However, the disease mechanisms that promote germinal matrix hemorrhage remain unclear. Here, we review recent advances using single-cell transcriptomics to uncover novel mechanisms that govern neurogenesis and angiogenesis in the germinal matrix of the prenatal human brain. These approaches also reveal the critical role of immune–vascular interaction that promotes vascular morphogenesis in the germinal matrix and how proinflammatory factors from activated neutrophils and monocytes can disrupt this process, leading to hemorrhage. Collectively, these results reveal fundamental disease mechanisms and therapeutic interventions for germinal matrix hemorrhage.
KW - angiogenesis
KW - germinal matrix
KW - immune–vascular interaction
KW - inflammation
KW - preterm birth
UR - https://www.scopus.com/pages/publications/85216822127
U2 - 10.1146/annurev-pathmechdis-111523-023446
DO - 10.1146/annurev-pathmechdis-111523-023446
M3 - Review article
C2 - 39401848
AN - SCOPUS:85216822127
SN - 1553-4006
VL - 20
SP - 221
EP - 243
JO - Annual Review of Pathology: Mechanisms of Disease
JF - Annual Review of Pathology: Mechanisms of Disease
IS - 1
ER -