Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Quick Search
My eDoc
Session History
Support Wiki
Direct access to
document ID:

          Institute: MPI für Herz- und Lungenforschung (W. G. Kerckhoff Institut)     Collection: Yearbook_2015     Display Documents

ID: 711916.0, MPI für Herz- und Lungenforschung (W. G. Kerckhoff Institut) / Yearbook_2015
Induction of angiotensin-converting enzyme after miR-143/145 deletion is critical for impaired smooth muscle contractility
Authors:Dahan, D.; Ekman, M.; Larsson-Callerfelt, A. K.; Turczynska, K.; Boettger, T.; Braun, T.; Sward, K.; Albinsson, S.
Date of Publication (YYYY-MM-DD):2014-12-15
Title of Journal:Am J Physiol Cell Physiol
Issue / Number:12
Start Page:C1093
End Page:101
Audience:Not Specified
Abstract / Description:MicroRNAs have emerged as regulators of smooth muscle cell phenotype with a role in smooth muscle-related disease. Studies have shown that miR-143 and miR-145 are the most highly expressed microRNAs in smooth muscle cells, controlling differentiation and function. The effect of miR-143/145 knockout has been established in the vasculature but not in smooth muscle from other organs. Using knockout mice we found that maximal contraction induced by either depolarization or phosphatase inhibition was reduced in vascular and airway smooth muscle but maintained in the urinary bladder. Furthermore, a reduction of media thickness and reduced expression of differentiation markers was seen in the aorta but not in the bladder. Supporting the view that phenotype switching depends on a tissue-specific target of miR-143/145, we found induction of angiotensin-converting enzyme in the aorta but not in the bladder where angiotensin-converting enzyme was expressed at a low level. Chronic treatment with angiotensin type-1 receptor antagonist restored contractility in miR-143/145-deficient aorta while leaving bladder contractility unaffected. This shows that tissue-specific targets are critical for the effects of miR-143/145 on smooth muscle differentiation and that angiotensin converting enzyme is one such target.
Free Keywords:Angiotensin II Type 1 Receptor Blockers/pharmacology; Animals; Aorta/drug effects/*enzymology/physiopathology; Dose-Response Relationship, Drug; Enzyme Induction; *Gene Deletion; Genotype; Mice, Knockout; MicroRNAs/genetics/*metabolism; *Muscle Contraction/drug effects; Muscle, Smooth, Vascular/drug effects/*enzymology/physiopathology; Organ Culture Techniques; Peptidyl-Dipeptidase A/*biosynthesis/genetics; Phenotype; Respiratory System/enzymology/physiopathology; Signal Transduction; Urinary Bladder/enzymology/physiopathology; *Vasoconstriction/drug effects; Vasoconstrictor Agents/pharmacology
External Publication Status:published
Document Type:Article
Communicated by:MPI für Herz- und Lungenforschung
Affiliations:MPI für physiologische und klinische Forschung
External Affiliations:Department of Biology, Lund University, Lund, Sweden; and. Max Planck Institute for Heart and Lung Research, Bad Nauheim, Germany. Department of Experimental Medical Science, Lund University, Lund, Sweden; sebastian.albinsson@med.lu.se. %^ 1435822261
Identifiers:ISSN:1522-1563 (Electronic) 0363-6143 (Linking) %R 10.1152/ajpcell.00250.2014
The scope and number of records on eDoc is subject to the collection policies defined by each institute - see "info" button in the collection browse view.