TY - JOUR
T1 - Membrane-bound and soluble Fas ligands have opposite functions in photoreceptor cell death following separation from the retinal pigment epithelium
AU - Matsumoto, H.
AU - Murakami, Y.
AU - Kataoka, K.
AU - Notomi, S.
AU - Mantopoulos, D.
AU - Trichonas, G.
AU - Miller, J. W.
AU - Gregory, M. S.
AU - Ksander, B. R.
AU - Marshak-Rothstein, A.
AU - Vavvas, D. G.
N1 - Funding Information:
Acknowledgements. We thank Wendy Chao for her support in critical review. This work was supported by Foundation Lions Eye Research Fund (DGV); The Yeatts Family Foundation (DGV and JWM); The Loefffler Family Foundation (DGV and JWM); 2013 Macula Society Research Grant award (DGV); Bausch & Lomb Vitreoretinal Fellowship (HM); Grant-in-Aid for Young Scientists (B) from Japan Society for the Promotion of Science (HM); Grant-in-Aid from Novartis Pharma K.K. Tokyo, Japan (HM); a RPB Physician Scientist Award (DGV) and unrestricted grant (JWM) from the Research to Prevent Blindness Foundation; NEI R21EY023079-01/ A1 (DGV) and NEI grant EY014104 (MEEI Core Grant). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Eye Institute or the National Institutes of Health.
Publisher Copyright:
© 2015 All rights reserved.
PY - 2015
Y1 - 2015
N2 - Fas ligand (FasL) triggers apoptosis of Fas-positive cells, and previous reports described FasL-induced cell death of Fas-positive photoreceptors following a retinal detachment. However, as FasL exists in membrane-bound (mFasL) and soluble (sFasL) forms, and is expressed on resident microglia and infiltrating monocyte/macrophages, the current study examined the relative contribution of mFasL and sFasL to photoreceptor cell death after induction of experimental retinal detachment in wild-type, knockout (FasL - / -), and mFasL-only knock-in (ΔCS) mice. Retinal detachment in FasL - / - mice resulted in a significant reduction of photoreceptor cell death. In contrast, ΔCS mice displayed significantly more apoptotic photoreceptor cell death. Photoreceptor loss in ΔCS mice was inhibited by a subretinal injection of recombinant sFasL. Thus, Fas/FasL triggered cell death accounts for a significant amount of photoreceptor cell loss following the retinal detachment. The function of FasL was dependent upon the form of FasL expressed: mFasL triggered photoreceptor cell death, whereas sFasL protected the retina, indicating that enzyme-mediated cleavage of FasL determines, in part, the extent of vision loss following the retinal detachment. Moreover, it also indicates that treatment with sFasL could significantly reduce photoreceptor cell loss in patients with retinal detachment.
AB - Fas ligand (FasL) triggers apoptosis of Fas-positive cells, and previous reports described FasL-induced cell death of Fas-positive photoreceptors following a retinal detachment. However, as FasL exists in membrane-bound (mFasL) and soluble (sFasL) forms, and is expressed on resident microglia and infiltrating monocyte/macrophages, the current study examined the relative contribution of mFasL and sFasL to photoreceptor cell death after induction of experimental retinal detachment in wild-type, knockout (FasL - / -), and mFasL-only knock-in (ΔCS) mice. Retinal detachment in FasL - / - mice resulted in a significant reduction of photoreceptor cell death. In contrast, ΔCS mice displayed significantly more apoptotic photoreceptor cell death. Photoreceptor loss in ΔCS mice was inhibited by a subretinal injection of recombinant sFasL. Thus, Fas/FasL triggered cell death accounts for a significant amount of photoreceptor cell loss following the retinal detachment. The function of FasL was dependent upon the form of FasL expressed: mFasL triggered photoreceptor cell death, whereas sFasL protected the retina, indicating that enzyme-mediated cleavage of FasL determines, in part, the extent of vision loss following the retinal detachment. Moreover, it also indicates that treatment with sFasL could significantly reduce photoreceptor cell loss in patients with retinal detachment.
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U2 - 10.1038/cddis.2015.334
DO - 10.1038/cddis.2015.334
M3 - Article
C2 - 26583327
AN - SCOPUS:84989306652
SN - 2041-4889
VL - 6
JO - Cell Death and Disease
JF - Cell Death and Disease
IS - 11
M1 - e1986
ER -