Effect of Growth Factors on the Proliferation and Gene Expression of Human Meibomian Gland Epithelial Cells

被引:45
作者
Liu, Shaohui [1 ,2 ]
Kam, Wendy R. [1 ,2 ,3 ]
Ding, Juan [1 ,2 ,3 ]
Hatton, Mark P. [1 ,2 ,3 ,4 ]
Sullivan, David A. [1 ,2 ,3 ]
机构
[1] Schepens Eye Res Inst, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Dept Ophthalmol, Boston, MA USA
[3] Massachusetts Eye & Ear Infirm, Boston, MA 02114 USA
[4] Ophthalm Consultants Boston, Boston, MA USA
关键词
meibomian gland; growth factors; gene expression; PEROXISOME-PROLIFERATOR; ACTIVATED RECEPTORS; SEBACEOUS GLAND; CLONAL GROWTH; CYCLE REGULATION; CULTURE; SERUM; DIFFERENTIATION; KERATINIZATION; MODEL;
D O I
10.1167/iovs.12-11221
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE. We hypothesize that growth factors, including epidermal growth factor (EGF) and bovine pituitary extract (BPE), induce proliferation, but not differentiation (e.g., lipid accumulation), of human meibomian gland epithelial cells. We also hypothesize that these actions involve a significant upregulation of genes linked to cell cycle processes, and a significant downregulation of genes associated with differentiation. Our objective was to test these hypotheses. METHODS. Immortalized human meibomian gland and conjunctival epithelial cells were cultured for varying time periods in the presence or absence of EGF, BPE, EGF + BPE, or serum, followed by cell counting, neutral lipid staining, or RNA isolation for molecular biological procedures. RESULTS. Our studies show that growth factors stimulate a significant, time-dependent proliferation of human meibomian gland epithelial cells. These effects are associated with a significant upregulation of genes linked to cell cycle, DNA replication, ribosomes, and translation, and a significant decrease in those related to cell differentiation, tissue development, lipid metabolic processes, and peroxisome proliferator-activated receptor signaling. Serum-induced differentiation, but not growth factor-related proliferation, elicits a pronounced lipid accumulation in human meibomian gland epithelial cells. This lipogenic response is unique, and is not duplicated by human conjunctival epithelial cells. CONCLUSIONS. Our results demonstrate that EGF and BPE stimulate human meibomian gland epithelial cells to proliferate. Further, our findings show that action is associated with an upregulation of cell cycle and translation ontologies, and a downregulation of genetic pathways linked to differentiation and lipid biosynthesis.
引用
收藏
页码:2541 / 2550
页数:10
相关论文
共 52 条
[1]   Cell proliferation and lipid formation in hamster sebaceous gland cells [J].
Akimoto, N ;
Sato, T ;
Sakiguchi, T ;
Kitamura, K ;
Kohno, Y ;
Ito, A .
DERMATOLOGY, 2002, 204 (02) :118-123
[2]   The use of human serum in supporting the in vitro and in vivo proliferation of human conjunctival epithelial cells [J].
Ang, LPK ;
Tan, DTH ;
Seah, CJY ;
Beuerman, RW .
BRITISH JOURNAL OF OPHTHALMOLOGY, 2005, 89 (06) :748-752
[3]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[4]   PPARδ:: a dagger in the heart of the metabolic syndrome [J].
Barish, GD ;
Narkar, VA ;
Evans, RM .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (03) :590-597
[5]   The mechanisms of action of PPARs [J].
Berger, J ;
Moller, DE .
ANNUAL REVIEW OF MEDICINE, 2002, 53 :409-435
[6]   Mitogenic signaling and the relationship to cell cycle regulation in astrocytomas [J].
Besson, A ;
Yong, VW .
JOURNAL OF NEURO-ONCOLOGY, 2001, 51 (03) :245-264
[7]   Cell cycle molecular targets in novel anticancer drug discovery [J].
Buolamwini, JK .
CURRENT PHARMACEUTICAL DESIGN, 2000, 6 (04) :379-392
[8]   The cornified envelope: A model of cell death in the skin [J].
Candi, E ;
Schmidt, R ;
Melino, G .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (04) :328-340
[9]  
CREEK KE, 1995, ADV EXP MED BIOL, V375, P117
[10]   Be fit or be sick: Peroxisome proliferator-activated receptors are down the road [J].
Desvergne, B ;
Michalik, L ;
Wahli, W .
MOLECULAR ENDOCRINOLOGY, 2004, 18 (06) :1321-1332