Serum level of apoptosis inhibitor of macrophage in dogs with histiocytic sarcoma and its association with the disease

Author:

Uchida Mona1ORCID,Matsumiya Yuki1,Tsuboi Masaya2,Uchida Kazuyuki2,Nakagawa Takayuki3,Fujii Wataru4ORCID,Kobayashi Tetsuya5ORCID,Tsujimoto Hajime6ORCID,Ohmi Aki7ORCID,Tomiyasu Hirotaka6ORCID,Motegi Tomoki7ORCID,Maeda Shingo1ORCID,Momoi Yasuyuki1,Yonezawa Tomohiro1ORCID

Affiliation:

1. Department of Veterinary Clinical Pathobiology, Graduate School of Agricultural and Life Sciences The University of Tokyo Tokyo Japan

2. Department of Veterinary Pathology, Graduate School of Agricultural and Life Sciences The University of Tokyo Tokyo Japan

3. Laboratory of Veterinary Surgery, Graduate School of Agricultural and Life Sciences The University of Tokyo Tokyo Japan

4. Department of Animal Resource Sciences, Graduate School of Agricultural and Life Sciences The University of Tokyo Tokyo Japan

5. Japan Small Animal Cancer Center Saitama Japan

6. Department of Veterinary Internal Medicine, Graduate School of Agricultural and Life Sciences The University of Tokyo Tokyo Japan

7. Veterinary Medical Center, Graduate School of Agricultural and Life Sciences The University of Tokyo Tokyo Japan

Abstract

AbstractHistiocytic sarcoma (HS) is a rare neoplasm of macrophages or dendritic cells with a poor prognosis in dogs. As the apoptosis inhibitor of macrophage (AIM) is characteristically expressed in canine macrophages, we hypothesised that AIM is involved in the development or progression of HS in dogs. In this study, AIM expression in the tumour region and serum AIM levels in dogs with HS was assessed. Additionally, the effects of AIM overexpression on HS cell viability were investigated using a HS cell line that was selected from five validated HS cell lines. Immunohistochemistry showed that AIM expression was observed in the cytoplasm of the HS cells. CD36, a candidate AIM receptor, was also observed on the cell membrane of HS cells. When the serum AIM level was detected in 36 dogs with HS and 10 healthy dogs via western blot analysis, the AIM levels in the HS dogs were significantly higher than those in the controls. AIM mRNA expression in the 5 HS cell lines varied but was higher than that in the other tumour‐derived lines. Among the five HS cell lines, DH82 originally had lower AIM and the highest CD36 expression. When AIM was overexpressed in DH82, therein cell growth speed and invasion, apoptosis inhibition and phagocytic activity were strongly upregulated. These data suggest that elevated intra‐tumour expression of AIM could induce the progression of HS cells in dogs. Moreover, elevated serum AIM levels in dogs with HS could serve as a biomarker of HS.

Publisher

Wiley

Subject

General Veterinary

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