Title:Determination of Expression Patterns of Seven De-sumoylation Enzymes in Major Ocular Cell Lines
Volume: 18
Issue: 9
关键词:
SENP,FHL124,HLE,αTN4-1,N / N1003A,ARPE-19,去SUMO化
摘要: Purpose: Accumulated evidence have well established that protein sumoylation plays
multiple roles in various cellular processes. In the vertebrate eye, we and others have
demonstrated that sumoylation displays indispensable roles in regulating eye development. Various
ocular cell lines including human embryonic cell line (FHL124), the SV40-large T-transformed
human lens epithelial cell line (HLE), the SV40-large T-transformed mouse lens epithelial cell line
(αTN4-1), the rabbit lens epithelial cell line (N/N1003A) and the human retina pigment epithelial cell
line (ARPE-19) have been extensively used for studying various cellular functions and disease
processes including sumoylation functions, and mechanisms for cataract and age-related macular
degeneration (AMD). However, the sumoylation enzyme systems have not been well established.
Methods: FHL124, HLE, αTN4-1, N/N1003A and ARPE-19 were cultured in Dulbecco’s modified
eagle medium (DMEM) containing 10% FBS and 1% penicillin & streptomycin. The expression
levels of seven SENP mRNAs were analyzed with qRT-PCR, and the expression levels of seven
SENP proteins were detected with Western blot analysis.
Results: Using both qRT-PCR and Western blot analysis, we have obtained the followings: 1). The
3 human ocular cell lines, FHL124, HLE and ARPE-19 express all types of SENP mRNA and
proteins. 2). In mouse lens epithelial cell line αTN4-1, and rabbit lens epithelial cells line N/N1003A,
however, only the mRNAs for SENP1, 2, 3, 6 and 7 are expressed. At the protein level, SENP8 was
absent in both αTN4-1 and N/N1003A cells; 3). Each cell line has different dominant SENP
enzymes. For FHL124, SENP3, 5, 7 and 8 proteins are relatively dominant. SENP3, 5 and 6 are the
major de-sumoylation enzymes in HLE cells. Different from human lens epithelial cells, FHL124 and
HLE, human retina pigment epithelial cells (ARPE-19) have SENP3, 7, and 8 as the dominant
forms of de-sumoylation enzymes. For mouse lens epithelial cells, SENP1, 3 and 7 are the major
de-sumoylation enzymes. On the other hand, the rabbit lens epithelial cells have SENP1, 2 and 7
as the major isoforms.
Conclusion: Our results for the first time defined the differential expression patterns of the seven
types of de-sumoylation enzymes (SENPs) in 5 major ocular cell lines. These results help to
establish the basis for the future study of sumoylation functions and the related mechanisms in
vertebrate eye.