Tamamoto Takashi, Ohno Koichi, Goto-Koshino Yuko, Fujino Yasuhito, Tsujimoto Hajime
Department of Veterinary Internal Medicine, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.
Vet Immunol Immunopathol. 2012 Nov 15;150(1-2):47-52. doi: 10.1016/j.vetimm.2012.08.005. Epub 2012 Aug 17.
Serum amyloid A (SAA) is one of the major acute phase proteins in cats and humans. SAA concentrations increase in response to the inflammatory status and secondary amyloid A amyloidosis has been documented in cats. In order to control the SAA concentration, it is important to clarify how the SAA protein is metabolized. Although the details of SAA metabolism in the body remain unknown, human and murine research indicates that macrophages play a key role in SAA uptake. The objectives of this study were to demonstrate SAA uptake by feline macrophages and to evaluate the effects of lipopolysaccharide (LPS) and dexamethasone (Dex) on SAA uptake. The concentration of recombinant feline SAA added to a feline macrophage culture was decreased in a time-dependent manner and was significantly reduced after a 24-h incubation, as demonstrated by enzyme linked immunosorbent assay (ELISA). SAA uptake into feline peripheral macrophages was demonstrated by immunofluorescence microscopy. Pretreatment to macrophages with LPS did not affect this decrease in the SAA concentration, but this was significantly blocked by Dex pretreatment. In conclusion, SAA was incorporated by feline macrophages and pretreatment with Dex inhibited SAA uptake by macrophages in this study. Further investigation is needed to determine the molecules that influence SAA uptake by macrophages and the effect of clinical glucocorticoid usage on the SAA concentration in cats.
血清淀粉样蛋白A(SAA)是猫和人类主要的急性期蛋白之一。SAA浓度会随着炎症状态而升高,并且猫中已记录到继发性淀粉样蛋白A淀粉样变性。为了控制SAA浓度,弄清楚SAA蛋白的代谢方式很重要。尽管体内SAA代谢的细节仍不清楚,但人类和小鼠研究表明巨噬细胞在SAA摄取中起关键作用。本研究的目的是证明猫巨噬细胞对SAA的摄取,并评估脂多糖(LPS)和地塞米松(Dex)对SAA摄取的影响。如酶联免疫吸附测定(ELISA)所示,添加到猫巨噬细胞培养物中的重组猫SAA浓度呈时间依赖性降低,孵育24小时后显著降低。通过免疫荧光显微镜证实了SAA被摄取到猫外周巨噬细胞中。用LPS预处理巨噬细胞并不影响SAA浓度的降低,但Dex预处理可显著阻断这种降低。总之,在本研究中SAA被猫巨噬细胞摄取,Dex预处理可抑制巨噬细胞对SAA的摄取。需要进一步研究以确定影响巨噬细胞摄取SAA的分子以及临床使用糖皮质激素对猫SAA浓度的影响。