Actions of β-apo-carotenoids in differentiating cells: differential effects in P19 cells and 3T3-L1 adipocytes

  • Arch Biochem Biophys. 2015 Apr 15;572:2-10. doi: 10.1016/j.abb.2015.01.009.
Cynthia X Wang  1 Hongfeng Jiang  2 Jason J Yuen  2 Seung-Ah Lee  2 Sureshbabu Narayanasamy  3 Robert W Curley Jr  4 Earl H Harrison  5 William S Blaner  6
Affiliations
  • 1. Columbia College, Columbia University, New York, NY 10032, United States.
  • 2. College of Physicians and Surgeons, Columbia University, New York, NY 10032, United States.
  • 3. College of Pharmacy, The Ohio State University, Columbus, OH 43210, United States; Department of Human Nutrition, The Ohio State University, Columbus, OH 43210, United States.
  • 4. College of Pharmacy, The Ohio State University, Columbus, OH 43210, United States.
  • 5. Department of Human Nutrition, The Ohio State University, Columbus, OH 43210, United States.
  • 6. College of Physicians and Surgeons, Columbia University, New York, NY 10032, United States. Electronic address: [email protected].
Abstract

β-Apo-carotenoids, including β-apo-13-carotenone and β-apo-14'-carotenal, are potent retinoic acid receptor (RAR) antagonists in transactivation assays. We asked how these influence RAR-dependent processes in living cells. Initially, we explored the effects of β-apo-13-carotenone and β-apo-14'-carotenal on P19 cells, a mouse embryonal carcinoma cell line that differentiates into neurons when treated with all-trans-retinoic acid. Treatment of P19 cells with either compound failed to block all-trans-retinoic acid induced differentiation. Liquid chromatography tandem mass spectrometry studies, however, established that neither of these β-apo-carotenoids accumulates in P19 cells. All-trans-retinoic acid accumulated to high levels in P19 cells. This suggests that the uptake and metabolism of β-apo-carotenoids by some cells does not involve the same processes used for retinoids and that these may be cell type specific. We also investigated the effects of two β-apo-carotenoids on 3T3-L1 adipocyte marker gene expression during adipocyte differentiation. Treatment of 3T3-L1 adipocytes with either β-apo-13-carotenone or β-apo-10'-carotenoic acid, which lacks RAR antagonist activity, stimulated adipocyte marker gene expression. Neither blocked the inhibitory effects of a relatively large dose of exogenous all-trans-retinoic acid on adipocyte differentiation. Our data suggest that in addition to acting as transcriptional antagonists, some β-apo-carotenoids act through Other mechanisms to influence 3T3-L1 adipocyte differentiation.

Keywords
Adipose differentiation; All-trans-retinoic acid; Gene expression; Obesity; Retinoid; Transcription.
Products