Multiple Directional Differentiation Difference of Neonatal Rat Fibroblasts from Six Organs

被引:21
作者
Chang, Yuqiao [1 ,2 ]
Guo, Kang [3 ]
Li, Qiong [2 ]
Li, Cixia [2 ]
Guo, Zhikun [2 ]
Li, He [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Human Anat & Embryol, Wuhan 430030, Peoples R China
[2] Xinxiang Med Univ, Henan Key Lab Med Tissue Regenerat, Xinxiang 453003, Peoples R China
[3] Xinxiang Med Univ, Affiliated Hosp 3, Tumor Dept, Xinxiang 453003, Peoples R China
基金
中国国家自然科学基金;
关键词
Fibroblasts; Immunofluorescence stainning; Stem cell markers; Heterogeneity; Directed differentiation; MESENCHYMAL STROMAL CELLS; HUMAN DERMAL FIBROBLASTS; STEM-CELLS; MATRIX METALLOPROTEINASES; CARDIAC FIBROBLASTS; IN-VITRO; LIGAND; PROGENITORS; POPULATION; ACTIVATION;
D O I
10.1159/000445613
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background/Aims: Fibroblasts are abundantly distributed throughout connective tissues in the body and are very important in maintaining the structural and functional integrity. Recent reports have proved that fibroblasts and mesenchymal stem cells share much more in common than previously recognized. The aim of this study was to investigate comparative studies in fibroblasts on the differences in the expression of molecular markers and differentiation capacity from different organs. Methods: Combined trypsin/collagenase enzymes digestion method was used to isolate and culture the fibroblasts derived from heart, liver, spleen, lung, kidney and skin. Cell activity was determined by methyl thiazolyl tetrazolium (MTT) assay. Common molecular markers for fibroblasts such as vimentin, DDR2 and FSP1, stem cell markers nanog, c-kit and sca-1 were detected by RT-PCR, immunofluorescence and western blotting. The osteogenic, adipogenic and cardiogenic differentiations of fibroblasts were performed by inductive culture in special mediums, and analyzed by Alizarin red, Oil red O and immunofluorescence staining of cTnT respectively. Results: The proliferation rate of fibroblasts in lung was faster than in other five organs. Common molecular markers for fibroblasts were expressed differently in different organs. DDR2 was strongly expressed in fibroblasts in the heart, partly expressed in the heart, skin, liver and spleen. Interestingly, no expression of DDR2 was detected in liver and kidney. However, vimentin and FSP1 were consistently expressed in fibroblasts from skin, liver, kidney, spleen and lung. nanog expression in fibroblasts from lung was less than that from heart, skin, liver and spleen (P < 0.01). c-kit expression in fibroblasts from heart, skin and kidney was higher than that from spleen (P < 0.05), while the c-kit positive fibroblasts from liver was obviously higher than that from spleen (P < 0.01). But sca-1 expression in fibroblasts from lung was the lowest among six organs (P < 0.01). Directed differentiation in vitro had demonstrated that skin fibroblasts had the strongest multiple differentiation potential, and the next was cardiac fibroblasts. And fibroblasts in liver and kidney had the advantage in myocardial differentiation, while fibroblasts in spleen only had the advantage in osteogenic differentiation. Conclusions: There are obvious heterogeneity in molecular markers and muti-directional differentiation in fibroblasts from six organs. (C) 2016 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:157 / 171
页数:15
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