RRC ID 57651
著者 Baba N, Wang F, Iizuka M, Shen Y, Yamashita T, Takaishi K, Tsuru E, Matsushima S, Miyamura M, Fujieda M, Tsuda M, Sagara Y, Maeda N.
タイトル Induction of regional chemokine expression in response to human umbilical cord blood cell infusion in the neonatal mouse ischemia-reperfusion brain injury model.
ジャーナル PLoS One
Abstract Regenerative medicine using umbilical cord blood (UCB) cells shows promise for the treatment of cerebral palsy. Although the efficacy of this therapy has been seen in the clinic, the mechanisms by which UCB cells interact and aid in the improvement of symptoms are not clear. We explored the chemokine expression profile in damaged brain tissue in the neonatal mouse ischemia-reperfusion (IR) brain injury model that was infused with human UCB (hUCB) cells. IR brain injury was induced in 9-day-old NOD/SCID mice. hUCB cells were administered 3 weeks post brain injury. Chemokine expression profiles in the brain extract were determined at various time points. Inflammatory chemokines such as CCL1, CCL17, and CXCL12 were transiently upregulated by 24 hours post brain injury. Upregulation of other chemokines, including CCL5, CCL9, and CXCL1 were prolonged up to 3 weeks post brain injury, but most chemokines dissipated over time. There were marked increases in levels of CCL2, CCL12, CCL20, and CX3CL1 in response to hUCB cell treatment, which might be related to the new recruitment and differentiation of neural stem cells, leading to the induction of tissue regeneration. We propose that the chemokine expression profile in the brain shifted from responding to tissue damage to inducing tissue regeneration. hUCB cell administration further enhanced the production of chemokines, and chemokine networks may play an active role in tissue regeneration in neonatal hypoxic-ischemic brain injury.
巻・号 14(9)
ページ e0221111
公開日 2019-9-4
DOI 10.1371/journal.pone.0221111
PII PONE-D-19-07879
PMID 31483787
PMC PMC6726228
MeSH Animals Biomarkers Brain Injuries / etiology* Brain Injuries / pathology* Brain Injuries / therapy Chemokines / genetics* Chemokines / metabolism Cord Blood Stem Cell Transplantation* / methods Cytokines / metabolism Disease Models, Animal Fetal Blood / cytology* Humans Mice Mice, Inbred NOD Mice, SCID Reperfusion Injury / etiology* Reperfusion Injury / pathology* Reperfusion Injury / therapy
IF 2.74
引用数 1
リソース情報
研究用ヒト臍帯血幹細胞