TY - JOUR
T1 - Deposition of amyloid β protein (Aβ) subtypes [Aβ40 and Aβ42(43)] in canine senile plaques and cerebral amyoloid angiopathy
AU - Nakamura, Shin'ichiro
AU - Tamaoka, Akira
AU - Sawamura, Naoya
AU - Kiatipattanasakul, Wijit
AU - Nakayama, Hiroyuki
AU - Shoji, Shin'ichi
AU - Yoshikawa, Yasuhiro
AU - Doi, Kunio
N1 - Funding Information:
Acknowledgements The work of Dr. A. Tamaoka (co-author) was supported in part by grants from the University of Tsukuba, the Japanese Medical Society, and by Grants-in-Aid for Scientific Research from the Ministry of Education, Science, and Culture, Japan. The authors thank Asano Asami, MS, and Nobuhiro Suzuki, PhD (Discovery Research Division, Takeda Chemical Industries, Ibaraki, Japan) for their generous gifts of BA27, BC05, and BS85, and Shin’ichi Itagaki, DVM. PhD (Department of Biomedical Sci- ence, Faculty of Agriculture, The University of Tokyo) for his technical support for lectin histochemistry.
PY - 1997/10
Y1 - 1997/10
N2 - To clarify the immunohistochemical features of canine senile plaques (SPs) and cerebral amyloid angiopathy (CAA), the distribution of the amyloid β protein (Aβ) subtypes Aβ40 and Aβ42(43), Aβ precursor protein (APP), and glial cell reaction were examined in the brains of seven aged dogs (12-18 years). Aβ42(43) was found to be deposited in all types of SPs, whereas Aβ40 was deposited only in mature (classical and primitive) plaques. CAA, which was located along parenchymal and meningeal arterioles and capillaries, consisted of both subtypes of Aβ. APP was exhibited in normal and degenerative neurons and swollen neurites of mature plaques. It was, therefore, considered that Aβ42(43) in diffuse plaques might be derived from APP in neurons, while Aβ40 and Aβ42(43) in mature plaques might be generated from APP in swollen neurites in the plaque. In contrast to the case in humans, in whom deposition of Aβ40 and Aβ42(43) in the mature plaques is predominantly associated with microglial reaction, in dogs we found that it was closely associated with astroglial reaction. The present findings showed characteristics of canine SPs which are different from those of humans.
AB - To clarify the immunohistochemical features of canine senile plaques (SPs) and cerebral amyloid angiopathy (CAA), the distribution of the amyloid β protein (Aβ) subtypes Aβ40 and Aβ42(43), Aβ precursor protein (APP), and glial cell reaction were examined in the brains of seven aged dogs (12-18 years). Aβ42(43) was found to be deposited in all types of SPs, whereas Aβ40 was deposited only in mature (classical and primitive) plaques. CAA, which was located along parenchymal and meningeal arterioles and capillaries, consisted of both subtypes of Aβ. APP was exhibited in normal and degenerative neurons and swollen neurites of mature plaques. It was, therefore, considered that Aβ42(43) in diffuse plaques might be derived from APP in neurons, while Aβ40 and Aβ42(43) in mature plaques might be generated from APP in swollen neurites in the plaque. In contrast to the case in humans, in whom deposition of Aβ40 and Aβ42(43) in the mature plaques is predominantly associated with microglial reaction, in dogs we found that it was closely associated with astroglial reaction. The present findings showed characteristics of canine SPs which are different from those of humans.
KW - Alzheimer's disease
KW - Amyloid β protein
KW - Amyolid angiopathy
KW - Dog
KW - Senile plaque
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U2 - 10.1007/s004010050714
DO - 10.1007/s004010050714
M3 - Article
C2 - 9341932
AN - SCOPUS:0030830113
SN - 0001-6322
VL - 94
SP - 323
EP - 328
JO - Acta Neuropathologica
JF - Acta Neuropathologica
IS - 4
ER -