TY - JOUR
T1 - Deletion of Efemp1 is protective against the development of sub-rpe deposits in mouse eyes
AU - Stanton, James B.
AU - Marmorstein, Alan D.
AU - Zhang, Youwen
AU - Marmorstein, Lihua Y.
N1 - Funding Information:
The authors thank Samuel D. Cross for technical assistance, Gina Zhang for assistance with electron microscopy, and Jim Schwie-gerling for assistance with the argon laser system. Supported by National Institutes of Health Grants EY13847 (LYM), EY13160 (ADM), and EY21153 (ADM) and an unrestricted grant from Research to Prevent Blindness to the Department of Ophthalmology at the Mayo Clinic in Rochester, Minnesota.
Publisher Copyright:
© 2017 The Authors.
PY - 2017/3
Y1 - 2017/3
N2 - PURPOSE. EFEMP1 (fibulin-3) is mutated in Malattia Leventinese/Doyne’s honeycomb retinal dystrophy (ML/DHRD), an inherited macular dystrophy similar to AMD. Both ML/DHRD and AMD are characterized by the presence of sub-RPE deposits. Efemp1 knockout mice do not develop sub-RPE deposits. This study was to test whether sub-RPE deposits can be induced in Efemp1 knockout mice by experimentally applied stress conditions that cause wild-type mice to develop sub-RPE deposits. METHODS. Efemp1 knockout and control mice at 6, 18, or 24 months old were fed with a synthetic high-fat diet (HFD). Beginning 1 month after starting the HFD, one group of mice was exposed to cigarette smoke daily for 1 month, and another group of mice was subjected to photochemical injury every other day for 2 weeks from a 488-nm argon laser. After the treatments, histologic analysis was performed to assess whether sub-RPE deposits were induced. RESULTS. Basal laminar deposits (BLamDs), a form of sub-RPE deposits, were observed in the 18- and 24-month-old wild-type mice but not in Efemp1 knockout mice in any age groups after exposure to HFD and cigarette smoke or laser injury. CONCLUSIONS. Mice lacking fibulin-3 do not develop sub-RPE deposits. Environmental oxidative stressors (HFD/cigarette smoke or HFD/laser) known to cause BLamD formation in wild-type mice failed to induce BLamD formation in Efemp1 knockout mice. These results suggest that fibulin-3 is a central player in the development of BLamD, and deletion of fibulin-3 is protective against the development of BLamD.
AB - PURPOSE. EFEMP1 (fibulin-3) is mutated in Malattia Leventinese/Doyne’s honeycomb retinal dystrophy (ML/DHRD), an inherited macular dystrophy similar to AMD. Both ML/DHRD and AMD are characterized by the presence of sub-RPE deposits. Efemp1 knockout mice do not develop sub-RPE deposits. This study was to test whether sub-RPE deposits can be induced in Efemp1 knockout mice by experimentally applied stress conditions that cause wild-type mice to develop sub-RPE deposits. METHODS. Efemp1 knockout and control mice at 6, 18, or 24 months old were fed with a synthetic high-fat diet (HFD). Beginning 1 month after starting the HFD, one group of mice was exposed to cigarette smoke daily for 1 month, and another group of mice was subjected to photochemical injury every other day for 2 weeks from a 488-nm argon laser. After the treatments, histologic analysis was performed to assess whether sub-RPE deposits were induced. RESULTS. Basal laminar deposits (BLamDs), a form of sub-RPE deposits, were observed in the 18- and 24-month-old wild-type mice but not in Efemp1 knockout mice in any age groups after exposure to HFD and cigarette smoke or laser injury. CONCLUSIONS. Mice lacking fibulin-3 do not develop sub-RPE deposits. Environmental oxidative stressors (HFD/cigarette smoke or HFD/laser) known to cause BLamD formation in wild-type mice failed to induce BLamD formation in Efemp1 knockout mice. These results suggest that fibulin-3 is a central player in the development of BLamD, and deletion of fibulin-3 is protective against the development of BLamD.
KW - Efemp1
KW - Macular degeneration
KW - Sub-RPE deposits
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U2 - 10.1167/iovs.16-20955
DO - 10.1167/iovs.16-20955
M3 - Article
C2 - 28264101
AN - SCOPUS:85014609528
SN - 0146-0404
VL - 58
SP - 1455
EP - 1461
JO - Investigative Ophthalmology and Visual Science
JF - Investigative Ophthalmology and Visual Science
IS - 3
ER -