Literature DB >> 19807253

The effects of ERK1/2 inhibitor on the chondrogenesis of bone marrow- and adipose tissue-derived multipotent mesenchymal stromal cells.

Hye-Joung Kim1, Gun-Il Im.   

Abstract

This study tested the hypothesis that mitogen-activated protein kinase inhibitors suppress hypertrophy and enhance chondrogenesis during chondrogenesis of multipotent mesenchymal stromal cells (MSCs). The effects of PD98059 (an extracellular signal-regulated kinase-1/2 inhibitor) and SB203580 (a p38 inhibitor) were tested on bone marrow-derived MSCs (BMMSCs) and adipose tissue-derived MSCs (ATMSCs). In vitro pellet cultures were carried out using 2.5 x 10(5) MSCs in a chondrogenic medium containing 5 ng/mL of transforming growth factor-beta(2) (TGF-beta(2)) for BMMSCs, and 5 ng/mL of TGF-beta(2) and 100 ng/mL of bone morphogenetic protein-7 (BMP-7) for ATMSCs. From the 14th day of culture, the pellets were additionally treated with PD98059 or SB203580. After 14 more days of in vitro culture, pellets were harvested for analysis. PD98059 increased DNA content and glycosaminoglycan amount in BMMSCs and ATMSCs, whereas SB203580 had little effect. Collagen type I (COL1A1) mRNA decreased to almost a quarter in BMMSCs treated with PD98059. The mRNA levels of collagen type II (COL2A1) and SRY (sex determining region Y)-box 9 (SOX-9) increased several fold in both cells after PD98059 treatment, whereas SB203580 had only a slight effect. The gene expression of collagen type X (COL10A1) and runt-related transcription factor 2 (Runx-2) decreased by half after PD98059 treatment in BMMSCs, and decreased further in ATMSCs. SB203580 elevated COL10A1 and Runx-2 gene expression in both cell types. Safranin-O staining and immunohistochemistry generally mirrored findings from real-time PCR except for diminished expression of type I collagen in ATMSCS, and more pronounced decrease in type X collagen and Runx-2 in BMMSCs after PD98059 treatment. Our study demonstrated that PD98059 suppressed hypertrophy and promoted chondrogenesis of MSCs, and provides a ground for using them in cartilage tissue engineering.

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Year:  2010        PMID: 19807253     DOI: 10.1089/ten.TEA.2009.0070

Source DB:  PubMed          Journal:  Tissue Eng Part A        ISSN: 1937-3341            Impact factor:   3.845


  7 in total

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Authors:  Ming Pei; Fan He; Vincent L Kish
Journal:  Tissue Eng Part A       Date:  2011-09-21       Impact factor: 3.845

3.  PD98059-impregnated functional PLGA scaffold for direct tissue engineering promotes chondrogenesis and prevents hypertrophy from mesenchymal stem cells.

Authors:  Jong Min Lee; Jong Dae Kim; Eun Jo Oh; Se Heang Oh; Jin Ho Lee; Gun-Il Im
Journal:  Tissue Eng Part A       Date:  2013-12-11       Impact factor: 3.845

4.  Strategies to minimize hypertrophy in cartilage engineering and regeneration.

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Journal:  Genes Dis       Date:  2015-03-01

5.  Low-frequency, low-magnitude vibrations (LFLM) enhances chondrogenic differentiation potential of human adipose derived mesenchymal stromal stem cells (hASCs).

Authors:  Krzysztof Marycz; Daniel Lewandowski; Krzysztof A Tomaszewski; Brandon M Henry; Edward B Golec; Monika Marędziak
Journal:  PeerJ       Date:  2016-02-25       Impact factor: 2.984

6.  Differential effects of p38 and Erk1/2 on the chondrogenic and osteogenic differentiation of dental pulp stem cells.

Authors:  Pengfei Ba; Xiaoyu Duan; Guo Fu; Shuyan Lv; Pishan Yang; Qinfeng Sun
Journal:  Mol Med Rep       Date:  2017-05-10       Impact factor: 2.952

7.  Inhibition of BMP signaling with LDN 193189 can influence bone marrow stromal cell fate but does not prevent hypertrophy during chondrogenesis.

Authors:  Rose Ann G Franco; Eamonn McKenna; Pamela G Robey; Md Shaffiulah Shajib; Ross W Crawford; Michael R Doran; Kathryn Futrega
Journal:  Stem Cell Reports       Date:  2022-02-17       Impact factor: 7.294

  7 in total

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