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Leptin Receptor Compound Heterozygosity in Humans and Animal Models

Leptin and its receptor are essential for regulating food intake, energy expenditure, glucose homeostasis and fertility. Mutations within leptin or the leptin receptor cause early-onset obesity and hyperphagia, as described in human and animal models. The effect of both heterozygous and homozygous v...

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Detalles Bibliográficos
Autores principales: Berger, Claudia, Klöting, Nora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123313/
https://www.ncbi.nlm.nih.gov/pubmed/33922961
http://dx.doi.org/10.3390/ijms22094475
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author Berger, Claudia
Klöting, Nora
author_facet Berger, Claudia
Klöting, Nora
author_sort Berger, Claudia
collection PubMed
description Leptin and its receptor are essential for regulating food intake, energy expenditure, glucose homeostasis and fertility. Mutations within leptin or the leptin receptor cause early-onset obesity and hyperphagia, as described in human and animal models. The effect of both heterozygous and homozygous variants is much more investigated than compound heterozygous ones. Recently, we discovered a spontaneous compound heterozygous mutation within the leptin receptor, resulting in a considerably more obese phenotype than described for the homozygous leptin receptor deficient mice. Accordingly, we focus on compound heterozygous mutations of the leptin receptor and their effects on health, as well as possible therapy options in human and animal models in this review.
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spelling pubmed-81233132021-05-16 Leptin Receptor Compound Heterozygosity in Humans and Animal Models Berger, Claudia Klöting, Nora Int J Mol Sci Review Leptin and its receptor are essential for regulating food intake, energy expenditure, glucose homeostasis and fertility. Mutations within leptin or the leptin receptor cause early-onset obesity and hyperphagia, as described in human and animal models. The effect of both heterozygous and homozygous variants is much more investigated than compound heterozygous ones. Recently, we discovered a spontaneous compound heterozygous mutation within the leptin receptor, resulting in a considerably more obese phenotype than described for the homozygous leptin receptor deficient mice. Accordingly, we focus on compound heterozygous mutations of the leptin receptor and their effects on health, as well as possible therapy options in human and animal models in this review. MDPI 2021-04-25 /pmc/articles/PMC8123313/ /pubmed/33922961 http://dx.doi.org/10.3390/ijms22094475 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Berger, Claudia
Klöting, Nora
Leptin Receptor Compound Heterozygosity in Humans and Animal Models
title Leptin Receptor Compound Heterozygosity in Humans and Animal Models
title_full Leptin Receptor Compound Heterozygosity in Humans and Animal Models
title_fullStr Leptin Receptor Compound Heterozygosity in Humans and Animal Models
title_full_unstemmed Leptin Receptor Compound Heterozygosity in Humans and Animal Models
title_short Leptin Receptor Compound Heterozygosity in Humans and Animal Models
title_sort leptin receptor compound heterozygosity in humans and animal models
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8123313/
https://www.ncbi.nlm.nih.gov/pubmed/33922961
http://dx.doi.org/10.3390/ijms22094475
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