A novel mouse model for an inducible gene modification in the renal thick ascending limb

Author:

Bourqui Laurent1ORCID,Winter Denise V.2ORCID,Odermatt Alex2ORCID,Loffing-Cueni Dominique1,Loffing Johannes13ORCID

Affiliation:

1. Institute of Anatomy, University of Zurich, Zurich, Switzerland

2. Division of Molecular and Systems Toxicology, Department of Pharmaceutical Sciences, University of Basel, Basel, Switzerland

3. National Centre of Competence in Research “Kidney.CH”, University of Zurich, Zurich, Switzerland

Abstract

The renal thick ascending limb (TAL) is critical for renal control of fluid and ion homeostasis. However, the underlying molecular mechanisms that regulate TAL function are incompletely understood. This study describes a novel transgenic mouse model (Slc12a1-creERT2) for inducible and highly efficient gene targeting in the TAL that promises to ease physiological studies on the functional role of candidate regulatory genes.

Funder

Swiss National Science Foundation

SNF | Swiss National Centre of Competence in Research Kidney Control of Homeostasis

University of Zurich

Publisher

American Physiological Society

Subject

Physiology

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Inducible deletion of the prostaglandin EP3 receptor in kidney tubules of male and female mice has no major effect on water homeostasis;American Journal of Physiology-Renal Physiology;2024-09-01

2. Animal models to study cognitive impairment of chronic kidney disease;American Journal of Physiology-Renal Physiology;2024-06-01

3. Guidelines on antibody use in physiology research;American Journal of Physiology-Renal Physiology;2024-03-01

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