Transplantation of Human Fetal-Derived Neural Stem Cells Improves Cognitive Function Following Cranial Irradiation

被引:26
作者
Acharya, Munjal M. [1 ]
Christie, Lori-Ann [1 ]
Hazel, Thomas G. [2 ]
Johe, Karl K. [2 ]
Limoli, Charles L. [1 ]
机构
[1] Univ Calif Irvine, Dept Radiat Oncol, Irvine, CA 92697 USA
[2] Neuralstem Inc, Rockville, MD USA
基金
美国国家卫生研究院;
关键词
Human fetal-derived neural stem cells; Transplantation; Radiation; Cognition; Hippocampus; Novel place recognition; Fear conditioning; AMYOTROPHIC-LATERAL-SCLEROSIS; CENTRAL-NERVOUS-SYSTEM; POSTERIOR-FOSSA TUMORS; EARLY GENE ARC; HIPPOCAMPAL NEUROGENESIS; CLINICAL-TRIALS; SPINAL-CORD; PHASE-I; NEUROCOGNITIVE DYSFUNCTION; THERAPEUTIC IRRADIATION;
D O I
10.3727/096368913X670200
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Treatment of central nervous system (CNS) malignancies typically involves radiotherapy to forestall tumor growth and recurrence following surgical resection. Despite the many benefits of cranial radiotherapy, survivors often suffer from a wide range of debilitating and progressive cognitive deficits. Thus, while patients afflicted with primary and secondary malignancies of the CNS now experience longer local regional control and progression free survival, there remains no clinical recourse for the unintended neurocognitive sequelae associated with their cancer treatments. Multiple mechanisms contribute to disrupted cognition following irradiation, including the depletion of radiosensitive populations of stem and progenitor cells in the hippocampus. We have explored the potential of using intrahippocampal transplantation of human stem cells to ameliorate radiation-induced cognitive dysfunction. Past studies demonstrated the capability of cranially transplanted human embryonic (hESCs) and neural (hNSCs) stem cells to functionally restore cognition in rats 1 and 4 months after cranial irradiation. The present study employed an FDA-approved fetal-derived hNSC line capable of large scale-up under good manufacturing practice (GMP). Animals receiving cranial transplantation of these cells 1 month following irradiation showed improved hippocampal spatial memory and contextual fear conditioning performance compared to irradiated, sham surgery controls. Significant newly born (doublecortin positive) neurons and a smaller fraction of glial subtypes were observed within and nearby the transplantation core. Engrafted cells migrated and differentiated into neuronal and glial subtypes throughout the CA1 and CA3 subfields of the host hippocampus. These studies expand our prior findings to demonstrate that transplantation of fetal-derived hNSCs improves cognitive deficits in irradiated animals, as assessed by two separate cognitive tasks.
引用
收藏
页码:1255 / 1266
页数:12
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