TY - JOUR
T1 - Methylparaben and butylparaben alter multipotent mesenchymal stem cell fates towards adipocyte lineage
AU - Hu, Pan
AU - Overby, Haley
AU - Heal, Emily
AU - Wang, Shu
AU - Chen, Jiangang
AU - Shen, Chwan li
AU - Zhao, Ling
N1 - Funding Information:
The studies were supported by the funding from University of Tennessee, Knoxville and from the National Center For Complementary & Integrative Health of the National Institutes of Health under Award Number R15AT008733. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Center for Complementary & Integrative Health or the National Institutes of Health.
Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2017/8/15
Y1 - 2017/8/15
N2 - 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.
AB - 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.
KW - Adiposity
KW - C3H10T1/2
KW - Endocrine disrupting chemicals
KW - Multipotent mesenchymal stem cell
KW - Obesity
KW - Parabens
UR - http://www.scopus.com/inward/record.url?scp=85019970223&partnerID=8YFLogxK
U2 - 10.1016/j.taap.2017.05.019
DO - 10.1016/j.taap.2017.05.019
M3 - Article
C2 - 28527915
AN - SCOPUS:85019970223
SN - 0041-008X
VL - 329
SP - 48
EP - 57
JO - Toxicology and Applied Pharmacology
JF - Toxicology and Applied Pharmacology
ER -