Abnormal neurogenesis and cortical growth in congenital heart disease

被引:75
作者
Morton, Paul D. [1 ,2 ]
Korotcova, Ludmila [1 ,2 ]
Lewis, Bobbi K. [3 ]
Bhuvanendran, Shivaprasad [4 ]
Ramachandra, Shruti D. [1 ,2 ]
Zurakowski, David [5 ,6 ]
Zhang, Jiangyang [7 ,8 ]
Mori, Susumu [7 ,8 ]
Frank, Joseph A. [9 ]
Jonas, Richard A. [1 ,2 ]
Gallo, Vittorio [1 ]
Ishibashi, Nobuyuki [1 ,2 ]
机构
[1] Childrens Natl Hlth Syst, Ctr Neurosci Res, Washington, DC 20010 USA
[2] Childrens Natl Hlth Syst, Childrens Natl Heart Inst, Washington, DC 20010 USA
[3] NIH, Frank Lab & Lab Diagnost Radiol Res, Dept Radiol & Imaging Sci, Bethesda, MD 20892 USA
[4] Childrens Natl Hlth Syst, Med Genet Res Ctr, Washington, DC 20010 USA
[5] Harvard Med Sch, Childrens Hosp Boston, Dept Anesthesia, Boston, MA 02115 USA
[6] Harvard Med Sch, Childrens Hosp Boston, Dept Surg, Boston, MA 02115 USA
[7] Johns Hopkins Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
[8] Johns Hopkins Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Baltimore, MD 21205 USA
[9] Natl Inst Biomed Imaging & Bioengn, Intramural Res Program, NIH, Bethesda, MD 20892 USA
关键词
NEURAL STEM-CELLS; WHITE-MATTER INJURY; ADULT HUMAN BRAIN; SUBVENTRICULAR ZONE; NEURODEVELOPMENTAL OUTCOMES; CEREBRAL-CORTEX; HUMAN NEOCORTEX; VASCULAR NICHE; RADIAL GLIA; NEURONS;
D O I
10.1126/scitranslmed.aah7029
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Long-term neurological deficits due to immature cortical development are emerging as a major challenge in congenital heart disease (CHD). However, cellular mechanisms underlying dysregulation of perinatal corticogenesis in CHD remain elusive. The subventricular zone (SVZ) represents the largest postnatal niche of neural stem/progenitor cells (NSPCs). We show that the piglet SVZ resembles its human counterpart and displays robust postnatal neurogenesis. We present evidence that SVZ NSPCs migrate to the frontal cortex and differentiate into interneurons in a region-specific manner. Hypoxic exposure of the gyrencephalic piglet brain recapitulates CHD-induced impaired cortical development. Hypoxia reduces proliferation and neurogenesis in the SVZ, which is accompanied by reduced cortical growth. We demonstrate a similar reduction in neuroblasts within the SVZ of human infants born with CHD. Our findings demonstrate that SVZ NSPCs contribute to perinatal corticogenesis and suggest that restoration of SVZ NSPCs' neurogenic potential is a candidate therapeutic target for improving cortical growth in CHD.
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页数:15
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