Serum lipids, retinoic acid and phenol red differentially regulate expression of keratins K1, K10 and K2 in cultured keratinocytes

被引:13
作者
Aldehlawi, Hebah [1 ]
Usman, Saima [2 ]
Lalli, Anand [2 ]
Ahmad, Fatima [2 ]
Williams, Gianne [2 ]
Teh, Muy-Teck [2 ,3 ,4 ]
Waseem, Ahmad [2 ]
机构
[1] King Abdulaziz Univ, Coll Dent, Jeddah, Saudi Arabia
[2] Queen Mary Univ London, Ctr Oral Immunobiol & Regenerat Med, Inst Dent, Barts & London Sch Med & Dent, London, England
[3] Guizhou Med Univ, Affiliated Stomatol Hosp, China British Joint Mol Head & Neck Canc Res Lab, Guiyang, Guizhou, Peoples R China
[4] Guangzhou Med Univ, Canc Res Inst, Affiliated Canc Hosp & Inst, Guangzhou, Guangdong, Peoples R China
关键词
MESSENGER-RNA STABILITY; RECONSTITUTED HUMAN SKIN; PROTEIN-CODING REGION; FETAL BOVINE SERUM; GENE-EXPRESSION; STEM-CELLS; IN-VIVO; POSTTRANSCRIPTIONAL REGULATION; TERMINAL DIFFERENTIATION; COMMERCIAL PREPARATIONS;
D O I
10.1038/s41598-020-61640-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Abnormal keratinocyte differentiation is fundamental to pathologies such as skin cancer and mucosal inflammatory diseases. The ability to grow keratinocytes in vitro allows the study of differentiation however any translational value is limited if keratinocytes get altered by the culture method. Although serum lipids (SLPs) and phenol red (PR) are ubiquitous components of culture media their effect on differentiation is largely unknown. We show for the first time that PR and SLP themselves suppress expression of differentiation-specific keratins K1, K10 and K2 in normal human epidermal keratinocytes (NHEK) and two important cell lines, HaCaT and N/TERT-1. Removal of SLP increased expression of K1, K10 and K2 in 2D and 3D cultures, which was further enhanced in the absence of PR. The effect was reversed for K1 and K10 by adding all-trans retinoic acid (ATRA) but increased for K2 in the absence of PR. Furthermore, retinoid regulation of differentiation-specific keratins involves post-transcriptional mechanisms as we show KRT2 mRNA is stabilised whilst KRT1 and KRT10 mRNAs are destabilised in the presence of ATRA. Taken together, our results indicate that the presence of PR and SLP in cell culture media may significantly impact in vitro studies of keratinocyte differentiation.
引用
收藏
页数:14
相关论文
共 85 条
[1]   The monoclonal antibody EPR1614Y against the stem cell biomarker keratin K15 lacks specificity and reacts with other keratins [J].
Aldehlawi, Hebah ;
Niemiec, Katarzyna A. ;
Avisetti, Deepa R. ;
Lalli, Anand ;
Teh, Muy-Teck ;
Waseem, Ahmad .
SCIENTIFIC REPORTS, 2019, 9 (1)
[2]   ARED 3.0: the large and diverse AU-rich transcriptome [J].
Bakheet, Tala ;
Williams, Bryan R. G. ;
Khabar, Khalid S. A. .
NUCLEIC ACIDS RESEARCH, 2006, 34 :D111-D114
[3]   INVOLUCRIN SYNTHESIS AND TISSUE ASSEMBLY BY KERATINOCYTES IN NATURAL AND CULTURED HUMAN EPITHELIA [J].
BANKSSCHLEGEL, S ;
GREEN, H .
JOURNAL OF CELL BIOLOGY, 1981, 90 (03) :732-737
[4]   PHENOL RED IN TISSUE-CULTURE MEDIA IS A WEAK ESTROGEN - IMPLICATIONS CONCERNING THE STUDY OF ESTROGEN-RESPONSIVE CELLS IN CULTURE [J].
BERTHOIS, Y ;
KATZENELLENBOGEN, JA ;
KATZENELLENBOGEN, BS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (08) :2496-2500
[5]   BIS(4-HYDROXYPHENYL)[2-(PHENOXYSULFONYL)PHENYL]METHANE - ISOLATION AND STRUCTURE ELUCIDATION OF A NOVEL ESTROGEN FROM COMMERCIAL PREPARATIONS OF PHENOL RED (PHENOLSULFONPHTHALEIN) [J].
BINDAL, RD ;
KATZENELLENBOGEN, JA .
JOURNAL OF MEDICINAL CHEMISTRY, 1988, 31 (10) :1978-1983
[6]   LIPOPHILIC IMPURITIES, NOT PHENOLSULFONPHTHALEIN, ACCOUNT FOR THE ESTROGENIC ACTIVITY IN COMMERCIAL PREPARATIONS OF PHENOL RED [J].
BINDAL, RD ;
CARLSON, KE ;
KATZENELLENBOGEN, BS ;
KATZENELLENBOGEN, JA .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1988, 31 (03) :287-293
[7]   Epidermal stem cells of the skin [J].
Blanpain, Cedric ;
Fuchs, Elaine .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2006, 22 :339-373
[8]   Expression of keratin K2e in cutaneous and oral lesions - Association with keratinocyte activation, proliferation, and keratinization [J].
Bloor, BK ;
Tidman, N ;
Leigh, IM ;
Odell, E ;
Dogan, B ;
Wollina, U ;
Ghali, L ;
Waseem, A .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 162 (03) :963-975
[9]   REGULATION OF KERATIN GENE-EXPRESSION - THE ROLE OF THE NUCLEAR RECEPTORS FOR RETINOIC ACID, THYROID-HORMONE, AND VITAMIN-D3 [J].
BLUMENBERG, M ;
CONNOLLY, DM ;
FREEDBERG, IM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 98 (06) :S42-S49
[10]   Two Mechanisms Regulate Keratin K15 Expression In Keratinocytes: Role of PKC/AP-1 and FOXM1 Mediated Signalling [J].
Bose, Amrita ;
Teh, Muy-Teck ;
Hutchison, Iain L. ;
Wan, Hong ;
Leigh, Irene M. ;
Waseem, Ahmad .
PLOS ONE, 2012, 7 (06)