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Identification of the (pro)renin receptor as a novel regulator of low-density lipoprotein metabolism

Identification of the (pro)renin receptor as a novel regulator of low-density lipoprotein metabolism
Identification of the (pro)renin receptor as a novel regulator of low-density lipoprotein metabolism

Rationale: the (pro)renin receptor ([P]RR) interacts with (pro)renin at concentrations that are >1000× higher than observed under (patho)physiological conditions. Recent studies have identified renin-angiotensin system-independent functions for (P)RR related to its association with the vacuolar H(+)-ATPase.

Objective: to uncover renin-angiotensin system-independent functions of the (P)RR.

Methods and results: we used a proteomics-based approach to purify and identify (P)RR-interacting proteins. This resulted in identification of sortilin-1 (SORT1) as a high-confidence (P)RR-interacting protein, a finding which was confirmed by coimmunoprecipitation of endogenous (P)RR and SORT1. Functionally, silencing (P)RR expression in hepatocytes decreased SORT1 and low-density lipoprotein (LDL) receptor protein abundance and, as a consequence, resulted in severely attenuated cellular LDL uptake. In contrast to LDL, endocytosis of epidermal growth factor or transferrin remained unaffected by silencing of the (P)RR. Importantly, reduction of LDL receptor and SORT1 protein abundance occurred in the absence of changes in their corresponding transcript level. Consistent with a post-transcriptional event, degradation of the LDL receptor induced by (P)RR silencing could be reversed by lysosomotropic agents, such as bafilomycin A1.

Conclusions: our study identifies a renin-angiotensin system-independent function for the (P)RR in the regulation of LDL metabolism by controlling the levels of SORT1 and LDL receptor.

Adaptor Proteins, Vesicular Transport/genetics, Animals, CHO Cells, Chromatin Immunoprecipitation, Cricetulus, Endocytosis, HEK293 Cells, Hep G2 Cells, Hepatocytes/metabolism, Humans, Lipoproteins, LDL/metabolism, Protein Processing, Post-Translational, Proteolysis, Proteomics/methods, RNA Interference, Receptors, Cell Surface/genetics, Receptors, LDL/genetics, Transfection, Vacuolar Proton-Translocating ATPases/genetics
0009-7330
222-229
Lu, Xifeng
83d95286-3da9-4053-81ce-962e4202f7a2
Meima, Marcel E.
1de0e25a-1fb3-40c5-adf2-c2f91b9a03a9
Nelson, Jessica K.
7dc3f0c8-5a67-4467-a332-efd560a0630b
Sorrentino, Vincenzo
f0cb3b5b-3a17-4ab3-ab65-180a7ee50d8a
Loregger, Anke
35d8c1fe-e11e-481e-bd35-e8160c079231
Scheij, Saskia
7863fcb2-eeba-43ab-93d5-8c9c08ad4289
Dekkers, Dick H.W.
09f26f21-c6fc-4888-8104-a4c630050a53
Mulder, Monique T.
ff0ae050-3ae4-4506-a239-a6956b10d3dd
Demmers, Jeroen A.A.
5284b42d-faa4-4b5d-9761-72c23e3358f9
M.-Dallinga-Thie, Geesje
c9ad3913-9f7e-4338-907f-68f08ed3ce3d
Zelcer, Noam
c5eff664-b107-4a7c-9823-11ccb8149fbc
Danser, A.H. Jan
d96665a8-2a52-4cd0-9a2f-cb403ad1b0c5
Lu, Xifeng
83d95286-3da9-4053-81ce-962e4202f7a2
Meima, Marcel E.
1de0e25a-1fb3-40c5-adf2-c2f91b9a03a9
Nelson, Jessica K.
7dc3f0c8-5a67-4467-a332-efd560a0630b
Sorrentino, Vincenzo
f0cb3b5b-3a17-4ab3-ab65-180a7ee50d8a
Loregger, Anke
35d8c1fe-e11e-481e-bd35-e8160c079231
Scheij, Saskia
7863fcb2-eeba-43ab-93d5-8c9c08ad4289
Dekkers, Dick H.W.
09f26f21-c6fc-4888-8104-a4c630050a53
Mulder, Monique T.
ff0ae050-3ae4-4506-a239-a6956b10d3dd
Demmers, Jeroen A.A.
5284b42d-faa4-4b5d-9761-72c23e3358f9
M.-Dallinga-Thie, Geesje
c9ad3913-9f7e-4338-907f-68f08ed3ce3d
Zelcer, Noam
c5eff664-b107-4a7c-9823-11ccb8149fbc
Danser, A.H. Jan
d96665a8-2a52-4cd0-9a2f-cb403ad1b0c5

Lu, Xifeng, Meima, Marcel E., Nelson, Jessica K., Sorrentino, Vincenzo, Loregger, Anke, Scheij, Saskia, Dekkers, Dick H.W., Mulder, Monique T., Demmers, Jeroen A.A., M.-Dallinga-Thie, Geesje, Zelcer, Noam and Danser, A.H. Jan (2016) Identification of the (pro)renin receptor as a novel regulator of low-density lipoprotein metabolism. Circulation Research, 118 (2), 222-229. (doi:10.1161/CIRCRESAHA.115.306799).

Record type: Article

Abstract

Rationale: the (pro)renin receptor ([P]RR) interacts with (pro)renin at concentrations that are >1000× higher than observed under (patho)physiological conditions. Recent studies have identified renin-angiotensin system-independent functions for (P)RR related to its association with the vacuolar H(+)-ATPase.

Objective: to uncover renin-angiotensin system-independent functions of the (P)RR.

Methods and results: we used a proteomics-based approach to purify and identify (P)RR-interacting proteins. This resulted in identification of sortilin-1 (SORT1) as a high-confidence (P)RR-interacting protein, a finding which was confirmed by coimmunoprecipitation of endogenous (P)RR and SORT1. Functionally, silencing (P)RR expression in hepatocytes decreased SORT1 and low-density lipoprotein (LDL) receptor protein abundance and, as a consequence, resulted in severely attenuated cellular LDL uptake. In contrast to LDL, endocytosis of epidermal growth factor or transferrin remained unaffected by silencing of the (P)RR. Importantly, reduction of LDL receptor and SORT1 protein abundance occurred in the absence of changes in their corresponding transcript level. Consistent with a post-transcriptional event, degradation of the LDL receptor induced by (P)RR silencing could be reversed by lysosomotropic agents, such as bafilomycin A1.

Conclusions: our study identifies a renin-angiotensin system-independent function for the (P)RR in the regulation of LDL metabolism by controlling the levels of SORT1 and LDL receptor.

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More information

e-pub ahead of print date: 18 November 2015
Published date: 22 January 2016
Keywords: Adaptor Proteins, Vesicular Transport/genetics, Animals, CHO Cells, Chromatin Immunoprecipitation, Cricetulus, Endocytosis, HEK293 Cells, Hep G2 Cells, Hepatocytes/metabolism, Humans, Lipoproteins, LDL/metabolism, Protein Processing, Post-Translational, Proteolysis, Proteomics/methods, RNA Interference, Receptors, Cell Surface/genetics, Receptors, LDL/genetics, Transfection, Vacuolar Proton-Translocating ATPases/genetics

Identifiers

Local EPrints ID: 505327
URI: http://eprints.soton.ac.uk/id/eprint/505327
ISSN: 0009-7330
PURE UUID: 7d776c02-3c7a-4f92-8c05-2773b57e3f69
ORCID for Jessica K. Nelson: ORCID iD orcid.org/0000-0003-2866-5170

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Date deposited: 07 Oct 2025 16:34
Last modified: 08 Oct 2025 02:17

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Contributors

Author: Xifeng Lu
Author: Marcel E. Meima
Author: Jessica K. Nelson ORCID iD
Author: Vincenzo Sorrentino
Author: Anke Loregger
Author: Saskia Scheij
Author: Dick H.W. Dekkers
Author: Monique T. Mulder
Author: Jeroen A.A. Demmers
Author: Geesje M.-Dallinga-Thie
Author: Noam Zelcer
Author: A.H. Jan Danser

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