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. 2022 Jul 15;3:926627. doi: 10.3389/fragi.2022.926627

TABLE 1.

RPE changes during normal aging and AMD.

RPE changes References
Normal Aging Loss of melanin granules (Sarna et al., 2003; Kubasik-Juraniec et al., 2004)
Lipofuscin accumulation (Schmucker and Sachs, 2002; Kubasik-Juraniec et al., 2004)
Decreased RPE cell density and increased RPE cell size and multinucleation Chen et al. (2016)
Shortening of RPE microvilli Boulton and Dayhaw-Barker, (2001)
Increased BrM thickness and decreased BrM/choroid elasticity (Zarbin, 2004; Harris et al., 2017)
Drusen formation Bergen et al. (2019)
Basal laminar deposit van der Schaft et al. (1993)
Accumulation of iron Chen et al. (2009c)
RPE secretome changes Meyer et al. (2019)
Modest decrease in RPE phagocytosis Boulton and Dayhaw-Barker, (2001)
AMD (May) have more cellular senescence Tong and Wang, (2020)
(May) have more cell death
Large soft drusen formation Ambati et al. (2003)
Hyper- or hypopigmentation in RPE
Lipofuscin aggregation in RPE (Holz et al., 2001; Hwang et al., 2006; Ach et al., 2015)
High variable and thicker RPE layer Zanzottera et al. (2015)
Shedding, dissociation and sloughing RPE cells (may indicate EMT process)
More significantly decreased RPE phagocytosis Inana et al. (2018)
Reduced mitochondrial function (Saini et al., 2017; Ebeling et al., 2021)
Increased inflammation markers
RPE secretome changes (An et al., 2006; Meyer et al., 2019)