2019
DOI: 10.1186/s12886-018-1017-6
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All-trans retinoic acid stimulates the secretion of TGF-β2 via the phospholipase C but not the adenylyl cyclase signaling pathway in retinal pigment epithelium cells

Abstract: BackgroundBy investigating that (i) all-trans retinoic acid (ATRA) affects human retinal pigment epithelium (RPE) in expressing and secreting transforming growth factor (TGF)-β2 and (ii) U73122 (phospholipase C inhibitor) and SQ22536 (adenylyl cyclase inhibitor) regulate the ATRA-induced secretion of TGF-β2 in human RPE, we sought to interpret the signaling pathway of ATRA in promoting the development of myopia.MethodsThe RPE cell line (D407) was treated with (i) ATRA (10 μM), (ii) U73122 (5–40 μM) and ATRA (1… Show more

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Cited by 10 publications
(7 citation statements)
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“…However, with further development of myopia, axial lengthening of the eye can lead to loss of epithelial integrity, ultimately resulting in degeneration of the choroid and retina. Additionally, atRA promotes the secretion of TGF-β in RPE through the phospholipase C pathway [ 58 ].…”
Section: Discussionmentioning
confidence: 99%
“…However, with further development of myopia, axial lengthening of the eye can lead to loss of epithelial integrity, ultimately resulting in degeneration of the choroid and retina. Additionally, atRA promotes the secretion of TGF-β in RPE through the phospholipase C pathway [ 58 ].…”
Section: Discussionmentioning
confidence: 99%
“…Through the miR-328 -PAX6 axis, exogenous atRA could upregulate metalloproteinase-2 and downregulate collagen I and integrin β 1 in the scleral cells [ 38 ]. In addition, atRA could stimulate retinal pigment epithelium to secret TGF-β, another strong extracellular matrix remodeling promoter [ 39 ].…”
Section: Discussionmentioning
confidence: 99%
“…Primary human pigmented epithelial cells (HRPEs) were purchased from Angio-Proteomie (cAP-0037, Boston, MA, USA) and maintained in HRPECs Growth Medium (contains serum and growth supplements, cAP-33) following the manufacturer’s instructions. HRPE cells were plated in a 6-well plate and cultured for 24 h. Cells were washed once with PBS before being treated with MEM media (Lonza Bioscience) containing retinoic acid, dexamethasone, or vehicle control dimethyl sulfoxide (DMSO) for another 24 h 93 . Cells were washed three times with PBS before being lysed for total RNA extraction using NucleoSpin RNA, Mini Kit (Macherey-Nagel, Duren, Germany) following the manufacturer’s instructions.…”
Section: Methodsmentioning
confidence: 99%