| Literature DB >> 25475834 |
Zong-Jian Liu1, Chen Chen, Feng-Wu Li, Jia-Mei Shen, Yuan-Yuan Yang, Rehana K Leak, Xun-Ming Ji, Hui-Shan Du, Xiao-Ming Hu.
Abstract
In the past decade, the significant contribution of the spleen to ischemic brain damage has gained considerable attention in stroke research. As the largest natural reservoir of immune cells, the spleen establishes critical connections with the ischemic brain during the progression of stroke and mobilizes its cells to the site of injury. Multiple "alarm" signals released from the injured brain are essential for the initiation of brain-spleen communication. Spleen-derived cells, including neutrophils, lymphocytes, and monocytes/macrophages, are known to contribute significantly to ischemic brain damage. Understanding the dynamic splenic responses to stroke will not only provide insights into the evolvement of ischemic brain injury but will also identify potential targets for stroke treatment. Here, we review recent studies on the functions of the spleen in ischemic stroke. We have included a discussion of several therapeutic strategies that target splenic responses and reduce acute ischemic brain damage in preclinical studies. Future investigations on the effects of the spleen on long-term stroke recovery are highly warranted.Entities:
Keywords: Immune response; Spleen; Stroke; Therapeutic strategies
Mesh:
Year: 2014 PMID: 25475834 PMCID: PMC6495279 DOI: 10.1111/cns.12361
Source DB: PubMed Journal: CNS Neurosci Ther ISSN: 1755-5930 Impact factor: 5.243