# Emerging perspectives on the selective autophagy of melanosomes: melanophagy

**Authors:** Na Yeon Park, Seong Hyun Kim, Doo Sin Jo, Dong-Hyung Cho

PMC · DOI: 10.1038/s12276-025-01581-3 · Experimental & Molecular Medicine · 2025-11-14

## TL;DR

This paper explores melanophagy, a process that breaks down melanosomes, and suggests it could lead to new treatments for skin pigmentation disorders.

## Contribution

The paper introduces melanophagy as a novel regulatory mechanism for skin pigmentation and potential therapeutic target.

## Key findings

- Melanophagy selectively degrades excess or damaged melanosomes to regulate pigment levels.
- Specific proteins and signaling pathways are involved in tagging melanosomes for degradation.
- Modulating melanophagy could offer new treatments for pigmentation disorders like vitiligo.

## Abstract

Melanosomes are highly specialized organelles responsible for melanin synthesis, storage and transport in melanocytes, playing a central role in pigmentation and skin homeostasis. Although melanosome biogenesis and trafficking have been well characterized, emerging evidence emphasizes the importance of melanosome degradation in regulating pigment levels. Among the degradation pathways, melanophagy—a selective form of autophagy targeting melanosomes—has recently emerged as an important mechanism for the turnover of damaged, immature, or excess melanosomes. Here we highlight current insights into melanophagy mechanisms, including molecular regulators and signaling pathways. We also discuss the potential of modulating melanophagy as a novel cosmetic or therapeutic approach for managing hyperpigmentation, offering an alternative to traditional strategies focused solely on inhibiting melanin synthesis. By emphasizing the role of organelle clearance, melanophagy provides a new paradigm in the regulation of skin pigmentation.

The skin is our body’s largest organ, protecting us from environmental harm and helping with temperature control and sensation. Melanosomes are tiny organelles in skin cells that produce and store melanin, the pigment responsible for skin color. This article explores how melanosomes are broken down through a process of selective autophagy called melanophagy. Researchers have found that melanophagy helps maintain skin color by removing excess or damaged melanosomes. They used laboratory studies to understand how certain proteins and pathways regulate this process. For example, they discovered that specific proteins tag melanosomes for degradation, ensuring proper pigment balance. The study concludes that understanding melanophagy could lead to new treatments for pigmentation disorders such as vitiligo or hyperpigmentation. In the future, targeting melanophagy might offer safer ways to manage skin pigmentation without disrupting other cellular functions. This summary was initially drafted using artificial intelligence, then revised and fact-checked by the author.

## Linked entities

- **Diseases:** vitiligo (MONDO:0008661)

## Full-text entities

- **Diseases:** hyperpigmentation (MESH:D017495)
- **Chemicals:** melanin (MESH:D008543)

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12800028