Literature DB >> 28527915

Methylparaben and butylparaben alter multipotent mesenchymal stem cell fates towards adipocyte lineage.

Pan Hu1, Haley Overby1, Emily Heal1, Shu Wang2, Jiangang Chen3, Chwan-Li Shen4, Ling Zhao5.   

Abstract

Paraben esters and their salts are widely used as preservatives in cosmetics, personal care products, pharmaceuticals, and foods. We previously reported that parabens promoted adipocyte differentiation in vitro and increased adiposity but suppressed serum marker of bone formation in vivo. Here, we investigated the effects of parabens (methylparaben and butylparaben) on modulating cell fate of multipotent stem cell line C3H10T1/2. Both parabens modulated adipogenic, osteogenic, and chondrogenic differentiation of C3H10T1/2 cells in vitro. Butylparaben markedly promoted adipogenic differentiation, but suppressed osteogenic and chondrogenic differentiation whereas methylparaben showed similar but less pronounced effects. Moreover, butylparaben, but not methylparaben, was shown to activate peroxisome proliferator-activated receptor (PPAR) γ whereas neither of the paraben was shown to activate glucocorticoid receptor (GR) responsive reporter in C3H10T1/2 cells. The adipogenic effects of butylparaben were significantly attenuated by PPARγ knockdown, but not by GR knockdown. In contrast, paraben's effects on osteoblast differentiation were affected by both knockdowns. Collectively, the results demonstrate opposing effects of parabens on adipogenic and osteoblastogenic/chondrogenic differentiation of multipotent stem cells. In light of the recent findings that parabens are detected in human placenta and milk, our studies provide rationales to study paraben exposure during early development of life in the future.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Adiposity; C3H10T1/2; Endocrine disrupting chemicals; Multipotent mesenchymal stem cell; Obesity; Parabens

Mesh:

Substances:

Year:  2017        PMID: 28527915      PMCID: PMC5528845          DOI: 10.1016/j.taap.2017.05.019

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  60 in total

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