Neocortical Layer Formation of Human Developing Brains and Lissencephalies: Consideration of Layer-Specific Marker Expression

被引:62
作者
Saito, Takashi [1 ,2 ]
Hanai, Sae [1 ,2 ]
Takashima, Sachio [3 ]
Nakagawa, Eiji [2 ]
Okazaki, Shin [4 ]
Inoue, Takeshi [5 ]
Miyata, Rie [6 ]
Hoshino, Kyoko [7 ]
Akashi, Takumi [8 ]
Sasaki, Masayuki [2 ]
Goto, Yu-ichi [1 ]
Hayashi, Masaharu [6 ]
Itoh, Masayuki [1 ]
机构
[1] Natl Ctr Neurol & Psychiat, Dept Mental Retardat & Birth Defect Res, Kodaira, Tokyo 1878502, Japan
[2] Hosp Natl Ctr Neurol & Psychiat, Dept Child Neurol, Kodaira, Tokyo 1878551, Japan
[3] Int Univ Hlth & Welf, Yanagawa Inst Handicapped Children, Fukuoka 8320058, Japan
[4] Osaka City Gen Hosp, Dept Pediat, Osaka 5340021, Japan
[5] Osaka City Gen Hosp, Dept Pathol & Lab Med, Osaka 5340021, Japan
[6] Tokyo Metropolitan Inst Neurosci, Dept Clin Neuropathol, Fuchu, Tokyo 1838526, Japan
[7] Saitama Med Ctr, Dept Pediat, Kawagoe, Saitama 350, Japan
[8] Tokyo Med & Dent Univ, Dept Pathol & Lab Med, Tokyo 1138510, Japan
关键词
developing human neocortex; layer-specific marker; lissencephaly; DEVELOPING CEREBRAL-CORTEX; NEURONAL MIGRATION DISORDERS; ABSENT CORPUS-CALLOSUM; AMBIGUOUS GENITALIA; ABNORMAL GENITALIA; MOUSE; LIS1; DIFFERENTIATION; IDENTITY; SATB2;
D O I
10.1093/cercor/bhq125
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
To investigate layer-specific molecule expression in human developing neocortices, we performed immunohistochemistry of the layer-specific markers (TBR1, FOXP1, SATB2, OTX1, CUTL1, and CTIP2), using frontal neocortices of the dorsolateral precentral gyri of 16 normal controls, aged 19 gestational weeks to 1 year old, lissencephalies of 3 Miller-Dieker syndrome (MDS) cases, 2 X-linked lissencephaly with abnormal genitalia (XLAG) cases, and 4 Fukuyama-type congenital muscular dystrophy (FCMD) cases. In the fetal period, we observed SATB2+ cells in layers II-IV, CUTL1+ cells in layers II-V, FOXP1+ cells in layer V, OTX1+ cells in layers II or V, and CTIP2+ and TBR1+ cells in layers V and VI. SATB2+ and CUTL1+ cells appeared until 3 months of age, but the other markers disappeared after birth. Neocortices of MDS and XLAG infants revealed SATB2+, CUTL1+, FOXP1+, and TBR1+ cells diffusely located in the upper layers. In fetal FCMD neocortex, neurons labeled with the layer-specific markers located over the glia limitans. The present study provided new knowledge indicating that the expression pattern of these markers in the developing human neocortex was similar to those in mice. Various lissencephalies revealed abnormal layer formation by random migration.
引用
收藏
页码:588 / 596
页数:9
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