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Synergistic Effect in Neurological Recovery via Anti-Apoptotic Akt Signaling in Umbilical Cord Blood and Erythropoietin Combination Therapy for Neonatal Hypoxic-Ischemic Brain Injury
被引:12
作者:
Choi, Jee In
[1
,2
]
Choi, Joo-Wan
[2
]
Shim, Kyu-Ho
[2
]
Choung, Jin Seung
[2
]
Kim, Hyun-Jin
[2
]
Sim, Hye Ryeong
[2
]
Suh, Mi Ri
[1
,2
]
Jung, Joo Eun
[3
]
Kim, MinYoung
[1
,2
]
机构:
[1] CHA Univ, Sch Med, Dept Rehabil Med, CHA Bundang Med Ctr, Seongnam 13496, South Korea
[2] CHA Univ, Sch Med, Rehabil & Regenerat Res Ctr, Seongnam 13488, South Korea
[3] Univ Texas Hlth Sci Ctr Houston, Dept Neurol, McGovern Med Sch, Houston, TX 77030 USA
关键词:
cord blood cell therapy;
erythropoietin;
hypoxic-ischemic brain injury;
neurobehavioral recovery;
anti-apoptosis;
Akt signaling pathway;
CEREBRAL-PALSY;
NEURONAL APOPTOSIS;
CELLS;
RAT;
ACTIVATION;
PATHWAY;
NEUROGENESIS;
INVOLVEMENT;
MECHANISMS;
RESPONSES;
D O I:
10.3390/ijms222111995
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Our previous clinical studies demonstrated the synergistic therapeutic effect induced by co-administering recombinant human erythropoietin (rhEPO) in human umbilical cord blood (hUCB) therapy for children with cerebral palsy. However, the cellular mechanism beyond the beneficial effects in this combination therapy still needs to be elucidated. A hypoxic-ischemic encephalopathy (HIE) model of neonates, representing cerebral palsy, was prepared and randomly divided into five groups (hUCB+rhEPO combination, hUCB, and rhEPO treatments over HIE, HIE control, and sham). Seven days after, hUCB was administered intraperitoneally and the rhEPO injections were started. Neurobehavioral tests showed the best outcome in the combination therapy group, while the hUCB and rhEPO alone treatments also showed better outcomes compared with the control (p < 0.05). Inflammatory cytokines were downregulated by the treatments and attenuated most by the combination therapy (p < 0.05). The hUCB+rhEPO treatment also showed remarkable increase in phosphorylation of Akt and potentiation of anti-apoptotic responses with decreased Bax and increased Bcl-2 (p < 0.05). Pre-treatment of MK-2206, an Akt inhibitor, for the combination therapy depressed the anti-apoptotic effects. In conclusion, these findings suggest that the therapeutic effect of hUCB therapy might be potentiated by co-administration of rhEPO via augmentation of anti-inflammatory and anti-apoptotic responses related to the phosphorylation of Akt.
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页数:17
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