Single-cell analysis of the cellular heterogeneity and interactions in the injured mouse spinal cord.
Single-cell analysis of the cellular heterogeneity and interactions in the injured mouse spinal cord.
复制标题
受损小鼠脊髓中细胞异质性和相互作用的单细胞分析。
DOI:
10.1084/jem.20210040
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发表时间:
2021-08-02
期刊:
影响因子:
--
通讯作者:
Lee JK
中科院分区:
文献类型:
--
作者:
Milich LM;Choi JS;Ryan C;Cerqueira SR;Benavides S;Yahn SL;Tsoulfas P;Lee JK
This study uses single-cell RNA sequencing to investigate the transcriptional heterogeneity of all cell types known to comprise the acutely injured spinal cord in mice. The authors investigate both cell subtype heterogeneity and potential signaling interactions between myeloid, vascular, and macroglia cells. The wound healing process that occurs after spinal cord injury is critical for maintaining tissue homeostasis and limiting tissue damage, but eventually results in a scar-like environment that is not conducive to regeneration and repair. A better understanding of this dichotomy is critical to developing effective therapeutics that target the appropriate pathobiology, but a major challenge has been the large cellular heterogeneity that results in immensely complex cellular interactions. In this study, we used single-cell RNA sequencing to assess virtually all cell types that comprise the mouse spinal cord injury site. In addition to discovering novel subpopulations, we used expression values of receptor–ligand pairs to identify signaling pathways that are predicted to regulate specific cellular interactions during angiogenesis, gliosis, and fibrosis. Our dataset is a valuable resource that provides novel mechanistic insight into the pathobiology of not only spinal cord injury but also other traumatic disorders of the CNS.
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