Isolation, Characterization, Differentiation and Immunomodulatory Capacity of Mesenchymal Stromal/Stem Cells from Human Perirenal Adipose Tissue

被引:32
作者
Baer, Patrick C. [1 ]
Koch, Benjamin [1 ]
Hickmann, Elena [1 ]
Schubert, Ralf [2 ]
Cinatl, Jindrich, Jr. [3 ]
Hauser, Ingeborg A. [1 ]
Geiger, Helmut [1 ]
机构
[1] Goethe Univ, Univ Hosp, Dept Internal Med 3, Div Nephrol, D-60596 Frankfurt, Germany
[2] Goethe Univ, Univ Hosp, Dept Children & Adolescents, Div Allergol Pneumol & Cyst Fibrosis, D-60596 Frankfurt, Germany
[3] Goethe Univ, Univ Hosp, Inst Med Virol, D-60596 Frankfurt, Germany
关键词
mesenchymal stromal/stem cells; perirenal; adipose tissue; fat; characterization; stimulation; lipopolysaccharide; cytokines; cytomegalovirus; STEM-CELLS; IN-VITRO; EPITHELIAL DIFFERENTIATION; CYTOMEGALOVIRUS-INFECTION; CONDITIONED MEDIUM; EXPRESSION; KIDNEY; FAT; HETEROGENEITY; PATHOGENESIS;
D O I
10.3390/cells8111346
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mesenchymal stromal/stem cells (MSCs) are immature multipotent cells, which represent a rare population in the perivascular niche within nearly all tissues. The most abundant source to isolate MSCs is adipose tissue. Currently, perirenal adipose tissue is rarely described as the source of MSCs. MSCs were isolated from perirenal adipose tissue (prASCs) from patients undergoing tumor nephrectomies, cultured and characterized by flow cytometry and their differentiation potential into adipocytes, chondrocytes, osteoblasts and epithelial cells. Furthermore, prASCs were stimulated with lipopolysaccharide (LPS), lipoteichoic acid (LTA) or a mixture of cytokines (cytomix). In addition, prASC susceptibility to human cytomegalovirus (HCMV) was investigated. The expression of inflammatory readouts was estimated by qPCR and immunoassay. HCMV infection was analyzed by qPCR and immunostaining. Characterization of cultured prASCs shows the cells meet the criteria of MSCs and prASCs can undergo trilineage differentiation. Cultured prASCs can be induced to differentiate into epithelial cells, shown by cytokeratin 18 expression. Stimulation of prASCs with LPS or cytomix suggests the cells are capable of initiating an inflammation-like response upon stimulation with LPS or cytokines, whereas, LTA did not induce a significant effect on the readouts (ICAM-1, IL-6, TNF alpha, MCP-1 mRNA and IL-6 protein). HCMV broadly infects prASCs, showing a viral load dependent cytopathological effect (CPE). Our current study summarizes the isolation and culture of prASCs, clearly characterizes the cells, and demonstrates their immunomodulatory potential and high permissiveness for HCMV.
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