TY - JOUR
T1 - Fatty Acid-Binding Protein 3 Expression in the Brain and Skin in Human Synucleinopathies
AU - Oizumi, Hideki
AU - Yamasaki, Kenshi
AU - Suzuki, Hiroyoshi
AU - Hasegawa, Takafumi
AU - Sugimura, Yoko
AU - Baba, Toru
AU - Fukunaga, Kohji
AU - Takeda, Atsushi
N1 - Funding Information:
We gratefully acknowledge Maki Takahashi, Shiryu Takemura, and Kikuko Hamanaka for technical support. Funding. The funding for this study was provided by Grants-in-Aid for Scientific Research from the Project of Translational and Clinical Research Core Centers from the Japan Agency for Medical Research and Development (AMED) (grant numbers JP17dm0107071, and JP18dm0107071 to KF and AT) and the Ministry of Health, Labor and Welfare of Japan.
Publisher Copyright:
© Copyright © 2021 Oizumi, Yamasaki, Suzuki, Hasegawa, Sugimura, Baba, Fukunaga and Takeda.
PY - 2021/3/25
Y1 - 2021/3/25
N2 - Parkinson’s disease (PD) and multiple system atrophy are types of adult-onset neurodegenerative disorders named synucleinopathies, which are characterized by prominent intracellular α-synuclein (αSyn) aggregates. We have previously found that αSyn aggregates and the vulnerability of dopaminergic neurons in the mouse brain are partly associated with the expression of fatty acid-binding protein 3 (FABP3, heart FABP). However, it remains to be elucidated whether FABP3 accumulation is associated with αSyn aggregates in human tissues. Here, we histologically studied FABP3 expression in human tissues obtained from patients with synucleinopathies, patients with Alzheimer disease (AD) and controls. We found that (1) a variety of neurons expressed the FABP3 protein in human brain tissues, (2) FABP3 was colocalized with αSyn aggregates in the brains of individuals with synucleinopathies but not with amyloid β or p-tau aggregates in the brains of individuals with AD, and (3) FABP3 was not present in p-αSyn deposits in biopsied skin tissues from individuals with PD. These findings suggest that FABP3 expression is associated with αSyn aggregation in synucleinopathies and provide new insights into the involvement of FABP3 in synucleinopathies.
AB - Parkinson’s disease (PD) and multiple system atrophy are types of adult-onset neurodegenerative disorders named synucleinopathies, which are characterized by prominent intracellular α-synuclein (αSyn) aggregates. We have previously found that αSyn aggregates and the vulnerability of dopaminergic neurons in the mouse brain are partly associated with the expression of fatty acid-binding protein 3 (FABP3, heart FABP). However, it remains to be elucidated whether FABP3 accumulation is associated with αSyn aggregates in human tissues. Here, we histologically studied FABP3 expression in human tissues obtained from patients with synucleinopathies, patients with Alzheimer disease (AD) and controls. We found that (1) a variety of neurons expressed the FABP3 protein in human brain tissues, (2) FABP3 was colocalized with αSyn aggregates in the brains of individuals with synucleinopathies but not with amyloid β or p-tau aggregates in the brains of individuals with AD, and (3) FABP3 was not present in p-αSyn deposits in biopsied skin tissues from individuals with PD. These findings suggest that FABP3 expression is associated with αSyn aggregation in synucleinopathies and provide new insights into the involvement of FABP3 in synucleinopathies.
KW - Parkinson’s disease
KW - fatty acid-binding protein
KW - human
KW - multiple system atrophy
KW - α-synuclein
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U2 - 10.3389/fnagi.2021.648982
DO - 10.3389/fnagi.2021.648982
M3 - Article
AN - SCOPUS:85103813433
SN - 1663-4365
VL - 13
JO - Frontiers in Aging Neuroscience
JF - Frontiers in Aging Neuroscience
M1 - 648982
ER -