Complex Brain Malformations Associated with Chromosome 6q27 Gain that Includes THBS2, Which Encodes Thrombospondin 2, an Astrocyte-Derived Protein of the Extracellular Matrix

被引:7
作者
Burnside, Melissa N. [1 ]
Pyatt, Robert E. [1 ,2 ]
Hughes, Anna [2 ]
Baker, Peter B. [1 ,2 ]
Pierson, Christopher R. [1 ,2 ]
机构
[1] Ohio State Univ, Coll Med, Columbus, OH 43210 USA
[2] Nationwide Childrens Hosp, Dept Pathol & Lab Med, Columbus, OH USA
关键词
axon elongation; brain malformation; microcephaly; neuronal migration; sudden unexpected death in infancy; THBS2; thrombospondin; 2; NEURONAL DEVELOPMENT; MEDULLA-OBLONGATA; ABNORMALITIES; SUDDEN; DEATH; EXPRESSION; MICE;
D O I
10.2350/14-06-1516-CR.1
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
This case describes the autopsy findings of a 2-month-old male infant with extensive and severe developmental brain abnormalities, including microcephaly, neocortical neuronal layering abnormalities, leptomeningeal heterotopias, commissural agenesis, and cerebellar and brainstem hypoplasia. Microarray analysis identified a gain in chromosome band 6q27, which includes the entire coding region of THBS2. THSB2 encodes thrombospondin 2 (TSP2), an astrocyte secreted protein of the extracellular matrix that promotes synaptogenesis, neurite outgrowth, and cerebellar granule cell migration. Thrombospondin 2 is not a matrix structural protein; instead it serves as an extracellular modulator of cell function, so it is considered a matricellular protein. The neuropathological findings at autopsy are compatible with perturbations in several known functions of TSP2 and demonstrate that TSP2 dysregulation can have a significant negative impact on human brain development. Furthermore, this case demonstrates the important role of astrocytes in human brain development.
引用
收藏
页码:59 / 65
页数:7
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