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Showing 2 results for Mesenchymal Stem Cells

Vahide Vahideh Assadollahi , Masoume Jalalvand, Shahrokh Bagheri, Hamed Esmaiel Lashkarian ,
Volume 10, Issue 6 (11-2016)
Abstract

ABSTRACT

          Background and Objective: Multipotent placental amniotic membrane mesenchymal stem cells (MSCs) are capable of differentiating into specialized tissues under different conditions. The aim of this study was to induce differentiation of placental amniotic membrane MSCs from NMRI mouse into hepatocytes using liver extract.

         Methods: Placental amniotic membrane MSCs from a 14-day pregnant female mouse was used in this study. The cells were incubated with trypsin solution, followed by pipetting. The resulting suspension was cultured in 12-well plates. After confirming their mesenchymal nature, differentiation of the aforementioned cells was induced via exposure to 6, 18, 30 and 60 μg/ml of liver extract. On the 16th day of treatment, immunocytochemical reaction for albumin and periodic acid-Schiff (PAS) test were performed for detection of hepatocyte-like cells.

          Results: Change was observed in the shape of differentiating cells from spindle-like shape to polygonal shape. The immunocytochemical reaction of the differentiated cells was positive. PAS staining also confirmed the accumulation of glycogen particles in the aforementioned cells. Concentration of 6 μg/ml liver extract was found as the effective dose for induction of differentiation.

           Conclusion: The findings of this study show that the placental amniotic membrane-derived MSCs of mouse can differentiate in vitro from spindle-like cells to polygonal hepatocyte-like cells with large nuclei and under the influence of the liver.

Keywords: Placental Amniotic Membrane Mesenchymal Stem Cells, Hepatocyte, In Vitro.


Leila Pirdel, Maryam Safajoo, Masoud Maleki,
Volume 19, Issue 5 (9-2025)
Abstract

Background: Mesenchymal stem cells (MSCs) are well-known for their immune-modulatory properties. A subgroup of the nucleotide-binding oligomerization domain (NOD)-like receptors (NLRs) has been recently identified to play a regulatory role in immune and inflammatory responses. This study aims to analyze and compare the gene expression levels of the NOD-like receptor family pyrin domain-containing proteins (NLRPs), such as NLRP6 and NLRP12, in Wharton’s jelly-derived mesenchymal stem cells (WJ-MSCs) treated with interferon-gamma (IFN-γ), the pro-inflammatory cytokine, and untreated cells.
Methods: The immunophenotypic characterization of the isolated Wharton’s Jelly mesenchymal stem cells (WJ-MSCs) was conducted using flow cytometry. Next, they were cultured with or without IFN-γ, followed by a comparison of the expression levels of the NLRP6 and NLRP12 genes using quantitative PCR (qPCR).
Results: Treatment of cells with IFN-γ resulted in a statistically significant increase in NLRP12 gene expression compared to untreated cells. In contrast, the expression of NLRP6 did not differ significantly between cells with or without IFN-γ treatment.
Conclusion: The altered expression level of NLRP12 suggests its potential role in the inflammatory regulation mediated by WJ-MSCs in response to IFN exposure; however, further studies are needed to validate its role in experimental models of inflammatory-related diseases.


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