Center for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Department of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA.
Nat Neurosci. 2014 Jan;17(1):131-43. doi: 10.1038/nn.3599. Epub 2013 Dec 8.
Microglia are myeloid cells of the CNS that participate both in normal CNS function and in disease. We investigated the molecular signature of microglia and identified 239 genes and 8 microRNAs that were uniquely or highly expressed in microglia versus myeloid and other immune cells. Of the 239 genes, 106 were enriched in microglia as compared with astrocytes, oligodendrocytes and neurons. This microglia signature was not observed in microglial lines or in monocytes recruited to the CNS, and was also observed in human microglia. We found that TGF-β was required for the in vitro development of microglia that express the microglial molecular signature characteristic of adult microglia and that microglia were absent in the CNS of TGF-β1-deficient mice. Our results identify a unique microglial signature that is dependent on TGF-β signaling and provide insights into microglial biology and the possibility of targeting microglia for the treatment of CNS disease.
小胶质细胞是中枢神经系统中的髓样细胞,参与中枢神经系统的正常功能和疾病。我们研究了小胶质细胞的分子特征,鉴定了 239 个基因和 8 个 microRNAs,它们在小胶质细胞中特异性或高表达,而在髓样细胞和其他免疫细胞中不表达或低表达。在 239 个基因中,有 106 个基因在小胶质细胞中富集,而在星形胶质细胞、少突胶质细胞和神经元中则不富集。这种小胶质细胞特征在小胶质细胞系或募集到中枢神经系统的单核细胞中观察不到,也在人类小胶质细胞中观察到。我们发现,TGF-β 对于体外培养表达成年小胶质细胞特征性小胶质细胞分子特征的小胶质细胞是必需的,并且 TGF-β1 缺陷型小鼠的中枢神经系统中没有小胶质细胞。我们的结果确定了一个独特的小胶质细胞特征,该特征依赖于 TGF-β 信号转导,并为小胶质细胞生物学和靶向小胶质细胞治疗中枢神经系统疾病的可能性提供了见解。