Structural characterization of a novel polysaccharide from Panax notoginseng residue and its immunomodulatory activity on bone marrow dendritic cells

2020 ◽  
Vol 161 ◽  
pp. 797-809 ◽  
Author(s):  
Shengnan Liu ◽  
Ye Yang ◽  
Yuan Qu ◽  
Xiaoxi Guo ◽  
Xiaoyan Yang ◽  
...  
2020 ◽  
Vol 295 (42) ◽  
pp. 14430-14444 ◽  
Author(s):  
Mariano Malamud ◽  
Gustavo J. Cavallero ◽  
Adriana C. Casabuono ◽  
Bernd Lepenies ◽  
María de los Ángeles Serradell ◽  
...  

S-layer (glyco)-proteins (SLPs) form a nanostructured envelope that covers the surface of different prokaryotes and show immunomodulatory activity. Previously, we have demonstrated that the S-layer glycoprotein from probiotic Lactobacillus kefiri CIDCA 8348 (SLP-8348) is recognized by Mincle (macrophage inducible C-type lectin receptor), and its adjuvanticity depends on the integrity of its glycans. However, the glycan's structure has not been described so far. Herein, we analyze the glycosylation pattern of three SLPs, SLP-8348, SLP-8321, and SLP-5818, and explore how these patterns impact their recognition by C-type lectin receptors and the immunomodulatory effect of the L. kefiri SLPs on antigen-presenting cells. High-performance anion-exchange chromatography–pulse amperometric detector performed after β-elimination showed glucose as the major component in the O-glycans of the three SLPs; however, some differences in the length of hexose chains were observed. No N-glycosylation signals were detected in SLP-8348 and SLP-8321, but SLP-5818 was observed to have two sites carrying complex N-glycans based on a site-specific analysis and a glycomic workflow of the permethylated glycans. SLP-8348 was previously shown to enhance LPS-induced activation on both RAW264.7 macrophages and murine bone marrow–derived dendritic cells; we now show that SLP-8321 and SLP-5818 have a similar effect regardless of the differences in their glycosylation patterns. Studies performed with bone marrow–derived dendritic cells from C-type lectin receptor–deficient mice revealed that the immunostimulatory activity of SLP-8321 depends on its recognition by Mincle, whereas SLP-5818's effects are dependent on SignR3 (murine ortholog of human DC-SIGN). These findings encourage further investigation of both the potential application of these SLPs as new adjuvants and the protein glycosylation mechanisms in these bacteria.


2014 ◽  
Vol 62 (4) ◽  
pp. 902-911 ◽  
Author(s):  
Yongshuai Jing ◽  
Lijiao Huang ◽  
Wenjie Lv ◽  
Hui Tong ◽  
Liyan Song ◽  
...  

Immunology ◽  
2001 ◽  
Vol 103 (3) ◽  
pp. 301-309 ◽  
Author(s):  
Jau-Ling Suen ◽  
Chung-Hsiun Wu ◽  
Ying-Yu Chen ◽  
Wen-Mein Wu ◽  
Bor-Luen Chiang

1999 ◽  
Vol 196 (1) ◽  
pp. 34-40 ◽  
Author(s):  
Lesya M. Pinchuk ◽  
Geraldine Grouard-Vogel ◽  
Dario M. Magaletti ◽  
Raymond T. Doty ◽  
Robert G. Andrews ◽  
...  

1996 ◽  
Vol 59 (2) ◽  
pp. 196-207 ◽  
Author(s):  
M. Chen-Woan ◽  
C.P. Delaney ◽  
V. Foumier ◽  
Y. Wakizaka ◽  
N. Murase ◽  
...  

2004 ◽  
Vol 77 (2) ◽  
pp. 104-115 ◽  
Author(s):  
R. Nunez ◽  
N. Garay ◽  
A. Bruno ◽  
C. Villafane ◽  
E. Bruno ◽  
...  

Immunology ◽  
2009 ◽  
Vol 129 (1) ◽  
pp. 133-145 ◽  
Author(s):  
Zhiguang Wu ◽  
Lisa Rothwell ◽  
John R. Young ◽  
Jim Kaufman ◽  
Colin Butter ◽  
...  

2007 ◽  
Vol 15 (1) ◽  
pp. 35-41 ◽  
Author(s):  
R. Keith Reeves ◽  
Patricia N. Fultz

ABSTRACT Plasmacytoid dendritic cells (pDCs), one of two types of bone marrow (BM)-derived blood DCs, play an important role in linking innate and adaptive immune responses. However, little is known about the nature of pDCs that reside in the BM. Because the simian immunodeficiency virus-macaque model closely mimics human immunodeficiency virus disease in humans, with both infections inducing a decrease in pDCs, we characterized and compared pDCs in the BM with those in peripheral blood (PB) of healthy pig-tailed macaques. The results revealed that pDCs from both compartments had the same CD123++ HLA-DR+ Lin− phenotype and were similar in size. Although BM-derived pDCs (BM-pDCs) were 3-fold greater in frequency and 10-fold greater in number, they had lower cell surface expression of both HLA-DR and the costimulatory molecule CD86 than did PB-pDCs. Both BM- and PB-pDCs responded ex vivo to synthetic CpG oligodeoxynucleotides and inactivated influenza virus by upregulating HLA-DR and CD86 and secreting cytokines; however, stimulated BM-pDCs secreted less alpha interferon and tumor necrosis factor alpha per cell than did PB-pDCs. These results suggest that while BM-pDCs appear to be phenotypically less mature than PB-pDCs, they do respond to pathogens. Thus, during acute infections, these cells could initiate immune responses either in the BM or after rapidly migrating from the BM into the periphery. A better characterization of pDCs in blood and tissues will be beneficial for future studies of macaques that focus on either pathogenesis or vaccine development.


Sign in / Sign up

Export Citation Format

Share Document