Vsig4

Case study 1: Zhutian Zeng, 2016

Kupffer cells (KCs), the vast pool of intravascular macrophages in the liver, help to clear blood-borne pathogens. The mechanisms by which KCs capture circulating pathogens remain unknown. Here the researchers use intra-vital imaging of mice infected with Staphylococcus aureus to directly visualize the dynamic process of bacterial capture in the liver. Circulating S. aureus were captured by KCs in a manner dependent on the macrophage complement receptor CRIg, but the process was independent of complement. CRIg bound Staphylococcus aureus specifically through recognition of lipoteichoic acid (LTA), but not cell-wall-anchored surface proteins or peptidoglycan. Blocking the recognition between CRIg and LTA in vivo diminished the bacterial capture in liver and led to systemic bacterial dissemination. All tested Gram-positive, but not Gram-negative, bacteria bound CRIg in a complement-independent manner. These findings reveal a pattern recognition role for CRIg in the direct capture of circulating Gram-positive bacteria from the bloodstream.

Fig1. Recombinant mouse (upper) or human (below) CRIg were labeled with AF-647.

Fig2. Quantification of the binding of AF647-labeled CRIg to various bacteria strains based on the geometric mean fluorescence intensity of AF 647 acquired by flow cytometry.

Case study 2: Yunmei Liao, 2014

Tumor-associated macrophages are a prominent component of lung cancer stroma and contribute to tumor progression. The protein V-set and Ig domain-containing 4 (VSIG4), a novel B7 family-related macrophage protein that has the capacity to inhibit T-cell activation, has a potential role in the development of lung cancer. Results showed massive VSIG4(+) cell infiltration throughout the samples. Immunofluorescent double staining showed that VSIG4 was present on CD68(+) macrophages, but absent from CD3(+) T cells, CD31(+) endothelial cells, and CK-18(+) epithelial cells. Moreover, VSIG4 was coexpressed on B7-H1(+) and B7-H3(+) cells in these tumor specimens.

Transfection of the VSIG4 gene into 293FT cells demonstrated that the VSIG4 signal could inhibit cocultured CD4(+) and CD8(+) T-cell proliferation and cytokine (IL-2 and IFN-γ) production in vitro. Interestingly, in a murine tumor model induced by Lewis lung carcinoma cell line, the researchers found that tumors grown in VSIG4-deficient (VSIG4(-/-)) mice were significantly smaller than those found in wild-type littermates. All of these results demonstrate that macrophage-associated VSIG4 is an activator that facilitates lung carcinoma development. Specific targeting of VSIG4 may prove to be a novel, efficacious strategy for the treatment of this carcinoma.

Fig3. The 293FT cells were transfected with lentivirus-expressing VSIG4 or empty lentivirus (gray shadow), and VSIG4 expression was confirmed by fluorescence-activated cell sorter (FACS).

Fig4. Purified CD4+ and CD8+ T cells were cocultured with 293FT or 293FT-VSIG4 cells, and cell proliferation was measured by 3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) after 3 days.

Fig1. Alcohol reduces the clearance of pathobionts by Kupffer cells and contributes to liver disease. (Yi Duan, 2021)

Fig2. Working model for the role of TRIM72 in regulating bacterial phagocytosis and inflammation. (Nagaraja Nagre, 2018)

Vsig4 involved in several pathways and played different roles in them. We selected most pathways Vsig4 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with Vsig4 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

Vsig4 has several biochemical functions, for example, protein binding. Some of the functions are cooperated with other proteins, some of the functions could acted by Vsig4 itself. We selected most functions Vsig4 had, and list some proteins which have the same functions with Vsig4. You can find most of the proteins on our site.

Vsig4 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with Vsig4 here. Most of them are supplied by our site. Hope this information will be useful for your research of Vsig4.

PDK2