Unknown

Dataset Information

0

Visualization of lipid directed dynamics of perilipin 1 in human primary adipocytes.


ABSTRACT: Perilipin 1 is a lipid droplet coating protein known to regulate lipid metabolism in adipocytes by serving as a physical barrier as well as a recruitment site for lipases to the lipid droplet. Phosphorylation of perilipin 1 by protein kinase A rapidly initiates lipolysis, but the detailed mechanism on how perilipin 1 controls lipolysis is unknown. Here, we identify specific lipid binding properties of perilipin 1 that regulate the dynamics of lipolysis in human primary adipocytes. Cellular imaging combined with biochemical and biophysical analyses demonstrate that perilipin 1 specifically binds to cholesteryl esters, and that their dynamic properties direct segregation of perilipin 1 into topologically distinct micro domains on the lipid droplet. Together, our data points to a simple unifying mechanism that lipid assembly and segregation control lipolysis in human primary adipocytes.

SUBMITTER: Hansen JS 

PROVIDER: S-EPMC5678101 | biostudies-literature | 2017 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Visualization of lipid directed dynamics of perilipin 1 in human primary adipocytes.

Hansen Jesper S JS   de Maré Sofia S   Jones Helena A HA   Göransson Olga O   Lindkvist-Petersson Karin K  

Scientific reports 20171108 1


Perilipin 1 is a lipid droplet coating protein known to regulate lipid metabolism in adipocytes by serving as a physical barrier as well as a recruitment site for lipases to the lipid droplet. Phosphorylation of perilipin 1 by protein kinase A rapidly initiates lipolysis, but the detailed mechanism on how perilipin 1 controls lipolysis is unknown. Here, we identify specific lipid binding properties of perilipin 1 that regulate the dynamics of lipolysis in human primary adipocytes. Cellular imagi  ...[more]

Similar Datasets

| S-EPMC3938729 | biostudies-other
| S-EPMC5854662 | biostudies-literature
| S-EPMC6971249 | biostudies-literature
| S-EPMC3667186 | biostudies-literature
| S-EPMC5909993 | biostudies-literature
| S-EPMC6724522 | biostudies-literature
| S-EPMC3690948 | biostudies-literature
| S-EPMC3063154 | biostudies-literature
| S-EPMC6962152 | biostudies-literature
| S-EPMC7595579 | biostudies-literature