Subducted and melanotic cells in advanced age-related macular degeneration are derived from retinal pigment epithelium
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Updated: Apr 11, 2026

Efficient Derivation of Retinal Pigment Epithelium Cells from Stem Cells
Published on: March 8, 2015
Emma C Zanzottera1, Jeffrey D Messinger2, Thomas Ach3
1Department of Ophthalmology University of Alabama School of Medicine, Birmingham, Alabama, United States 2Eye Clinic, Department of Clinical Science "Luigi Sacco," Sacco Hospital, University of Milan, Milan, Italy.
Purpose:
To describe, illustrate, and account for two cell types plausibly derived from RPE in geographic atrophy (GA) and choroidal neovascularization (CNV) of AMD, using melanosomes, lipofuscin, and basal laminar deposit (BLamD) as anatomical markers.
Methods:
Human donor eyes with GA (n = 13) or CNV (n = 39) were histologically processed, photodocumented, and analyzed for frequencies of occurrence. We defined RPE as cells containing spindle-shaped melanosomes and RPE lipofuscin, internal to basal lamina or BLamD, if present, or Bruch's membrane if not, and RPE-derived cells as those plausibly derived from RPE and not attached to basal lamina or BLamD.
Results:
'Subducted' cells contain RPE melanosomes and localize to the sub-RPE space, on Bruch's membrane. Credible transitional forms from RPE cells were seen. Grades of RPE overlying 'Subducted' cells were 'Atrophic with BLamD' (32.2% vs. 37.0% of 'Subducted,' for GA and CNV eyes, respectively), 'Dissociated' (22.0% vs. 21.7%), 'Nonuniform' (22.0% vs. 23.9%), and 'Sloughed' RPE (10.2% vs. 4.3%). Found exclusively in CNV scars, 'Melanotic' cells containing spherical melanosomes were adjacent to 'Entombed' RPE with spindle-shaped and spherical melanosomes. Of subretinal 'Melanotic' cells, 40.0% associated with 'Atrophy with BLamD,' 36.8% with 'Atrophy without BLamD,' and 20.6% with 'Entombed.'
Conclusions:
'Dissociated' RPE within atrophic areas may be the source of 'Subducted' cells. 'Entombed' RPE within fibrovascular and fibrocellular scars may be the source of 'Melanotic' cells. An imaging correlate for 'Subducted' cells awaits discovery; 'Melanotic' cells appear gray-black in the CNV fundus. Results provide a basis for future molecular phenotyping studies.
Insights
Researchers identified two novel cell types, "Subducted" and "Melanotic" cells, originating from retinal pigment epithelium (RPE) cells in age-related macular degeneration (AMD). These findings offer insights into AMD pathogenesis and potential therapeutic targets.
Area of Science:
- Ophthalmology
- Cell Biology
- Pathology
Background:
- Age-related macular degeneration (AMD) is a leading cause of vision loss.
- Geographic atrophy (GA) and choroidal neovascularization (CNV) are hallmarks of advanced AMD.
- The cellular origins of pathological changes in AMD remain incompletely understood.
Purpose of the Study:
- To identify and characterize two distinct cell types potentially derived from retinal pigment epithelium (RPE) in GA and CNV.
- To utilize melanosomes, lipofuscin, and basal laminar deposit (BLamD) as anatomical markers for cell identification.
- To elucidate the cellular mechanisms underlying AMD progression.
Main Methods:
- Histological analysis of human donor eyes with GA (n=13) and CNV (n=39).
- Photodocumentation and frequency analysis of identified cell types.
- Definition of RPE and RPE-derived cells based on melanosome morphology, lipofuscin presence, and location relative to basal lamina and Bruch's membrane.
Main Results:
- 'Subducted' cells, containing RPE melanosomes, were found in the sub-RPE space, with transitional forms observed.
- 'Melanotic' cells, exclusively in CNV scars, contained spherical melanosomes and were adjacent to 'Entombed' RPE.
- Specific associations were noted between 'Subducted' cells and RPE atrophy with BLamD, and between 'Melanotic' cells and CNV scars.
Conclusions:
- 'Dissociated' RPE cells may give rise to 'Subducted' cells in atrophic AMD.
- 'Entombed' RPE cells in scars may be the source of 'Melanotic' cells.
- Further molecular phenotyping studies are warranted to confirm these findings and explore their clinical implications.
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