PMID- 7545567 OWN - NLM STAT- MEDLINE DCOM- 19951013 LR - 20190830 IS - 0271-3683 (Print) IS - 0271-3683 (Linking) VI - 14 IP - 6 DP - 1995 Jun TI - SV40-immortalized and primary cultured human retinal pigment epithelial cells share similar patterns of cytokine-receptor expression and cytokine responsiveness. PG - 495-503 AB - Retinal pigment epithelial (RPE) cells produce and respond to a variety of cytokines; however, molecular and biochemical studies are restricted by the limited access to large numbers of pure cells and the variability associated with different donor sources. Despite success in establishing primary human RPE (HRPE) cell cultures, the inability to sustain consistent proliferation rates and morphology over several passages remains a concern. This problem was approached by using an immortalized line of simian virus (SV)40 transformed fetal HRPE cells (SVRPE). Cytokine production, receptor expression and responsiveness in the SVRPE cell line was analyzed to determine the usefulness of this model for studying HRPE-cytokine interactions. Using reverse transcriptase polymerase chain reaction (RT-PCR), HRPE and SVRPE cells demonstrated an identical pattern of interleukin-1 receptor (IL-1R), IL-2R (alpha sub-unit), IL-6R, interferon (IFN)-gamma R and tumor necrosis factor-alpha (TNF)R p55 expression. No amplification products for TNFR p75 or granulocyte/macrophage colony stimulating factor (GM-CSF)R were demonstrated in either population. IFN-gamma stimulation induced surface human leukocyte antigen (HLA)-DR in both SVRPE and HRPE, while TNF treatment induced surface expression of intercellular adhesion molecule (ICAM)-1 on SVRPE and upregulated ICAM from basal levels on HRPE. Both cell types showed amplification products for interleukin (IL)-1 beta, IL-6 and transforming growth factor (TGF)-beta 1 using RT-PCR. The bioassays demonstrated that both populations of unstimulated cells constitutively secrete very low levels of TGF-beta and no IL-6.(ABSTRACT TRUNCATED AT 250 WORDS) FAU - Sippy, B D AU - Sippy BD AD - Department of Pathology, University of Southern California School of Medicine, Los Angeles 90033, USA. FAU - Hofman, F M AU - Hofman FM FAU - He, S AU - He S FAU - Osusky, R AU - Osusky R FAU - Sheu, S J AU - Sheu SJ FAU - Walker, S M AU - Walker SM FAU - Ryan, S J AU - Ryan SJ FAU - Hinton, D R AU - Hinton DR LA - eng GR - R01-EY02061/EY/NEI NIH HHS/United States PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - England TA - Curr Eye Res JT - Current eye research JID - 8104312 RN - 0 (Cytokines) RN - 0 (DNA Probes) RN - 0 (RNA, Messenger) RN - 0 (Receptors, Cytokine) RN - EC 2.7.7.49 (RNA-Directed DNA Polymerase) SB - IM MH - Base Sequence MH - Cell Division MH - Cell Line, Transformed MH - Cell Transformation, Viral/physiology MH - Cells, Cultured MH - Cytokines/biosynthesis/*pharmacology MH - DNA Probes/chemistry MH - Flow Cytometry MH - Humans MH - Molecular Sequence Data MH - Pigment Epithelium of Eye/cytology/drug effects/*metabolism MH - Polymerase Chain Reaction MH - RNA, Messenger/metabolism MH - RNA-Directed DNA Polymerase MH - Receptors, Cytokine/*biosynthesis MH - Simian virus 40/physiology EDAT- 1995/06/01 00:00 MHDA- 1995/06/01 00:01 CRDT- 1995/06/01 00:00 PHST- 1995/06/01 00:00 [pubmed] PHST- 1995/06/01 00:01 [medline] PHST- 1995/06/01 00:00 [entrez] AID - 10.3109/02713689509003761 [doi] PST - ppublish SO - Curr Eye Res. 1995 Jun;14(6):495-503. doi: 10.3109/02713689509003761.