Preservation of hematopoietic properties in transplanted bone marrow cells in the brain

被引:34
作者
Ono, K
Yoshihara, K
Suzuki, H
Tanaka, KF
Takii, T
Onozaki, K
Sawada, M [1 ]
机构
[1] Fujita Hlth Univ, Joint Res Div Therapies Against Intractable Dis, Inst Comprehens Med Sci, Joint Res Div,Therapies Against Intractable Dis, Toyoake, Aichi 4701192, Japan
[2] Nagoya City Univ, Grad Sch Pharmaceut Sci, Dept Mol Hlth Sci, Nagoya, Aichi, Japan
关键词
bone marrow transplantation; transdifferentiation; ER-MP12; green fluorescent protein; microglia;
D O I
10.1002/jnr.10588
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent studies have described the possible transdifferentiation of bone marrow cells (BMC) into neurons and glia when they migrate to the brain. However, we have reported that some immature BMC migrating into the brain parenchyma after bone marrow transplantation express early hematopoietic markers but not neural or glial markers. The present study further characterizes transplanted BMC that migrate to the brain. Double immunolabeling confirmed that BMC migrating to the brain expressed hematopoietic but not neural markers, such as nestin, microtubule-associated protein-2 and glial fibrillary acidic protein, even 4 and 18 weeks after bone marrow transplantation. BMC that expressed green fluorescent protein also expressed hematopoietic but not neural markers when cultured with mixed brain cells according to double immunolabeling and single-cell dissection using a laser. Analysis of the DNA content indicated that most of the migrated BMC were arrested at the G0/G1 phase, and aneuploidy or tetraploidy was undetectable. Thus, BMC that migrate to the brain probably have preserved hematopoietic properties under physiological conditions. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:503 / 507
页数:5
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