TY - JOUR
T1 - Demyelination in severe combined immunodeficient mice by intracisternal injection of cerebrospinal fluid cells from patients with multiple sclerosis
T2 - Neuropathological investigation
AU - Fujimura, Harutoshi
AU - Nakatsuji, Yuji
AU - Sakoda, Saburo
AU - Toyooka, Keiko
AU - Okuda, Yoshinobu
AU - Yoshikawa, Hiroo
AU - Kaido, Misako
AU - Saeki, Yukihiko
AU - Mima, Toru
AU - Kishimoto, Tadamitsu
AU - Yanagihara, Takehiko
N1 - Funding Information:
Acknowledgements The authors are grateful to Ms. C. Kato, K. Yamamori and A. Kanasaka for their technical assistance. This study was supported, in part, by a Grant-in-Aid for Specially Promoted Research, and a Grant-in-Aid for Scientic Research (C) from the Ministry of Education, Science and Culture, Japan, and by Amgen Inc.
PY - 1997/6
Y1 - 1997/6
N2 - Demyelinating lesions have been observed in severe combined immunodeficient (SCID) mice after intracisternal administration of cerebrospinal fluid cells (CSFC) from patients with multiple sclerosis (MS). Further investigation in our laboratory revealed that CSFC from 6 of 15 patients at exacerbation of MS caused demyelination. The factor leading to demyelination appears to be the high frequency of relapses during a short period, but not the severity of the disease. Neuropathological and immunohistochemical studies revealed that a lack of inflammatory mononuclear cell infiltration within and around the demyelinating lesions or in leptomeninges was a common characteristic in all SCID mice with CSFC-induced demyelination. In affected mice killed 2-3 weeks after intracisternal administration of CSFC, foamy/vacuolar lesions with a small or moderate number of lipid-laden macrophages were seen in the white mater. Ultrastructurally, relative preservation of axons, in contrast to myelinoclastic features, as well as some remyelinated axons were observed. In affected SCID mice killed 4-6 weeks after intracisternal administration, more widespread foamy macrophages and necrotic foci with poor remyelination were seen. The findings were similar to those seen in experimental allergic encephalomyelitis, though without lymphocytic infiltration, but were quite different from the lesions observed in Theiler's murine encephalitis virus infection. The absence of an immunohistochemical reaction to the human leukocyte common antigen in the infiltrating mononuclear cells suggested that the graft-versus-host reaction was an unlikely cause of the demyelinating lesions.
AB - Demyelinating lesions have been observed in severe combined immunodeficient (SCID) mice after intracisternal administration of cerebrospinal fluid cells (CSFC) from patients with multiple sclerosis (MS). Further investigation in our laboratory revealed that CSFC from 6 of 15 patients at exacerbation of MS caused demyelination. The factor leading to demyelination appears to be the high frequency of relapses during a short period, but not the severity of the disease. Neuropathological and immunohistochemical studies revealed that a lack of inflammatory mononuclear cell infiltration within and around the demyelinating lesions or in leptomeninges was a common characteristic in all SCID mice with CSFC-induced demyelination. In affected mice killed 2-3 weeks after intracisternal administration of CSFC, foamy/vacuolar lesions with a small or moderate number of lipid-laden macrophages were seen in the white mater. Ultrastructurally, relative preservation of axons, in contrast to myelinoclastic features, as well as some remyelinated axons were observed. In affected SCID mice killed 4-6 weeks after intracisternal administration, more widespread foamy macrophages and necrotic foci with poor remyelination were seen. The findings were similar to those seen in experimental allergic encephalomyelitis, though without lymphocytic infiltration, but were quite different from the lesions observed in Theiler's murine encephalitis virus infection. The absence of an immunohistochemical reaction to the human leukocyte common antigen in the infiltrating mononuclear cells suggested that the graft-versus-host reaction was an unlikely cause of the demyelinating lesions.
KW - Cerebrospinal fluid
KW - Demyelination
KW - Experimental allergic encephalomyelitis
KW - Multiple sclerosis
KW - Severe combined immunodeficient mouse
UR - http://www.scopus.com/inward/record.url?scp=0030916611&partnerID=8YFLogxK
U2 - 10.1007/s004010050653
DO - 10.1007/s004010050653
M3 - 学術論文
C2 - 9194895
AN - SCOPUS:0030916611
SN - 0001-6322
VL - 93
SP - 567
EP - 578
JO - Acta Neuropathologica
JF - Acta Neuropathologica
IS - 6
ER -