# Lipid droplet dynamics in metabolic regulation

**Authors:** Ralf Weiskirchen, Sabine Weiskirchen, Amedeo Lonardo

PMC · DOI: 10.1039/d6cb00081a · RSC Chemical Biology · 2026-03-25

## TL;DR

Lipid droplets are dynamic organelles that regulate lipid storage and metabolism, with roles in metabolic diseases and potential as therapeutic targets.

## Contribution

This review synthesizes current understanding of lipid droplet dynamics, their interactions with other organelles, and emerging therapeutic opportunities.

## Key findings

- Lipid droplet dynamics are linked to metabolic diseases like obesity and liver disease.
- Tissue-specific lipid droplet biology influences systemic energy homeostasis.
- New imaging and chemical biology tools enable detailed study of lipid droplet function.

## Abstract

Lipid droplets (LDs) are ubiquitous intracellular organelles that store neutral lipids such as triacylglycerols and sterol esters within a phospholipid monolayer decorated by a specialized proteome. Far from being inert depots, LDs are highly dynamic hubs that integrate lipid storage with cellular and systemic metabolic regulation. Their biogenesis, growth, remodeling, and catabolism are tightly controlled by nutrient status, hormonal signaling, and cellular stress, and are coupled to key metabolic pathways including β-oxidation, lipogenesis, membrane synthesis, and signaling lipid production. Aberrant LD dynamics coexist with a broad spectrum of metabolic pathologies, from obesity and insulin resistance to metabolic dysfunction-associated steatotic liver disease, lipodystrophies, and cancer. In this review, we discuss current concepts of LD biogenesis and expansion, cytosolic lipolysis and lipophagy, and the physical and functional interactions of LDs with mitochondria, peroxisomes, endoplasmic reticulum, and lysosomes. We highlight how tissue-specific LD biology in adipose tissue, liver, skeletal muscle, pancreatic β-cells, and immune cells shapes systemic energy homeostasis and the response to metabolic stress. Particular emphasis is placed on chemical biology and imaging approaches that have transformed our ability to visualize and manipulate LDs in space and time, including fluorescent lipid probes, metabolic labeling, organelle-targeted proximity labeling, lipidomics, and functional screening. Finally, we outline the opportunities and challenges in therapeutically targeting LD dynamics for metabolic disorders. This includes the emerging concept of exploiting LDs as drug and nucleic acid delivery platforms. We also discuss the outstanding questions that need to be addressed in order to safely use LD biology for clinical benefit.

Lipid droplets are dynamic organelles for lipid storage and metabolic signaling. This review summarizes their biogenesis and turnover, tissue-specific roles in metabolic disease, and therapeutic targeting opportunities.

## Linked entities

- **Diseases:** obesity (MONDO:0011122), metabolic dysfunction-associated steatotic liver disease (MONDO:0013209), cancer (MONDO:0004992)

## Full-text entities

- **Diseases:** steatotic liver disease (MESH:D008107), metabolic disorders (MESH:D008659), cancer (MESH:D009369), insulin resistance (MESH:D007333), obesity (MESH:D009765), lipodystrophies (MESH:D008060)
- **Chemicals:** phospholipid (MESH:D010743), Lipid (MESH:D008055), triacylglycerols (MESH:D014280), sterol esters (-)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13034180/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13034180/full.md

## References

122 references — full list in the complete paper: https://tomesphere.com/paper/PMC13034180/full.md

---
Source: https://tomesphere.com/paper/PMC13034180