Cross-talk between mineralocorticoid and angiotensin II signaling for cardiac
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1 ONLINE SUPPLEMENT TO Crosstalk between mineralocorticoid and angiotensin II signaling for cardiac remodeling An Di ZHANG,,3, Aurelie NGUYEN DINH CAT*,,3, Christelle SOUKASEUM *,,3, Brigitte ESCOUBET, 4, 5, Aïcha CHERFA 5,6, Smail MESSAOUDI 3,7, Claude DELCAYRE 3,7, JaneLise SAMUEL 5,7, Frederic JAISSER,,3 Inserm, U77, Paris, F755, France; Collège de France, Paris F755, France ; 3 Univ Paris Descartes, Paris, F755, France, 4 Assistance PubliqueHôpitaux de Paris, Hôpital Bichat, Paris, F758, France ; 5 University Denis Diderot, Paris 7, Paris, F758, France; 6 EA 358, paris, F756, France ; 7 INSERM U689 ; Paris, F75, France. * These two authors contributed equally to the study Corresponding AUTHOR: Frederic JAISSER Tel / FAX: frederic.jaisser@collegedefrance.fr
2 Supplementary method Realtimepolymerase chain reaction (RTPCR) Total RNA was extracted from cardiac ventricle tissue using the TRIZOL reagent (Invitrogen, Carlsabad, CA). Briefly, µg of total RNA was reversetranscribed with units of reverse transcriptase using the Superscript II kit (Invitrogen, Carlsabad, CA) according to the manufacturer s recommendations. The RT products were then amplified on a MJ Research PTC PCR apparatus, using Taqman Gene Expression Assays for collagenia, collagen IIIa and Hypoxanthine Phospho Ribosyl Transferase (HPRT) as reference genes (Cola: Mm8666, Col3a: Mm833, HPRT: Mm446968). For gp9(nox), p47, p67, TNFa, ICAM, VCAM, icycle iq apparatus (Biorad Laboratories, Paris, France) was used for RTPCR with SYBER Green using primers described in Supplementary Table S. All samples were tested in duplicate and quantitative relative values were calculated by Delta DeltaCt method (Analysis of relative gene expression data using realtime quantitative PCR and the [delta delta C(T)] method) 4. Western blotting for p9, p47 and p67 proteins Heart samples were homogenized in sodium dodecylsulfate (SDS) lysis buffer containing a protease inhibitor cocktail (Roche Diagnostics, Meylan, France). Proteins ( µg) were separated by % SDSpolyacrylamide gel electrophoresis and transferred to nitrocellulose membranes (Amersham, Biosciences Europe GMBH, Orsay, France). The membranes were incubated with antigp9 (/, BD Transduction laboratories, Canada), antip47 or antip67 (/, Santa Cruz Biotechnologie, U.S.A). Bound antibody was visualized by using horseradish peroxidaseconjugated secondary antibody (Amersham) and ECL Plus reagents
3 (Amersham) and signals were acquired in a Las3 DarkBox (Fuji photo Film Europe GMBH, Düsseldorf, Germany). GAPDH was used as internal control for protein loading. Immunostaining with F4/8 Cryostat sections were dried in air, fixed in acetone, and incubated sequentially with a rat antimouse F4/8 antigen antibody (Abcam, UK) (:5), a biotinylated antirat IgG(HL) antibody (Vector, Burlingame, CA) an avidin/peroxidase complex (ABC kit; Vector); bound antibody was visualized with Histogreen (AbCys, France). 3
4 Supplementary Table Table S Primers sequences gene forward reverse CTGF 5' TGA CCC CTG CGA CCC ACA 3' 5' TAC ACC GAC CCA CCG AAG ACA CAG 3' fibronectin 5' CCG GTG GCT GTC AGT CAG A 3' 5' CCG TTC CCA CTG CTG ATT TAT C 3' P47phox 5' AGC TCC CAG GTG GTA TGA TG 3' 5' ATC TTT GGC CGT CAG GTA TG 3' P67phox 5' GCC GGA GAC GCC AGA AGA GCT A 3' 5' GGG GCT GCG ACT GAG GGT GAA 3' Gp9 5' CGC CCT TTG CCT CCA TTC TC 3' 5' CCT TTC CTG CAT CTG GGT CTC C 3' MCP 5' CAT GCT TCT GGG CCT GCT GTT C 3' 5' CCT GCT GCT GGT GAT CCT CTT G 3' CD68 5' TTC TGC TGT GGA AAT GCA AG 3' 5' AGA GGG GCT GGT AGG TTG AT 3' ICAM 5 TTC ACA CTG AAT GCC AGC TC 3 5 GTC TGC TGA GAC CCC TCT TG 3 VCAM 5 ATT TTC TGG GGC AGG AAG TT 3 5 ACG TCA GAA CAA CCG AAT CC3 TNFα 5 CAT CTT CTC AAA ACT CGA GTG ACA A 3 5 TGG GAG TAG ATA AGG TAC AGC CC 3 AT 5 ATT CAA CGC TCC CCA TAG GA3 5 TGA ATT TCA TAA GCC TTC TTT AGA GCT3 ACE 5 TGA GGT GAC CCT GCT GGC AAG GCC3 5 GTG CTG GGA CTG TCA AGG AGA CAG GC3 HPRT 5' CTC AAC TTT AAC TGG AAA GAA TGT C 3' 5' TCC TTT TCA CCA GCA AGC T 3' CTGF: connective tissue growth factor; MCP: Monocyte chemotactic protein; ICAM: intercellular adhesion molecule; VCAM: vascular cell adhesion molecule; TNFα: tumor necrosis factoralpha; AT: Angiotensin II receptor type I; ACE: angiotensinconverting enzyme; HPRT : Hypoxanthine Phospho Ribosyl Transferase; 4
5 Ctl Silent DTg Cardiac MR overexpression Ctl Ctl A CtlAC DTg DTg A DTgA C months Functional assessment and sampling Pathological and Molecular analyses Ctl: control, DTg: double transgenic, A: Angiotensin II, C: Canrenoate Figure S. Experimental protocol. Two monthold doubletransgenic MHCtTA/tetOhMR (DTg) male mice and their control littermates were divided in 6 groups: control (Ctl); control treated with (CtlA); control treated with and canrenoate (CtlAC); DTg mice (DTg); DTg mice treated with (DTgA); and DTg mice treated with and canrenoate (DTgAC). Angiotensin II was infused s.c. through an osmotic minipump for months and canrenoate given in the drinking water. The untreated mice were mock treated (the same procedure) with vehicle instead of. Functional assessments were done immediately before sacrifice. Figure S
6 4 3 * Fibronectin * * * * Canr Figure S. Effects of infusion, cardiac MR overexpression and the combination of both on fibronectin mrna expression. Open bars: Ctl mice, Filled bars: DTg mice. : treatment; Canr: Canrenoate treatment. * p<.5 versus Ctl, p<.5 versus DTg, p<.5 versus DTg Ang, n=7. Figure S
7 A,,8,4 ACE B 6 4 * AT * Figure S 3. Effects of infusion, cardiac M R overexpression and the combination of both on mrna expression of ACE (A) and AT (B). Open bars: Ctl mice, Filled bars: DTg mice. : treatment. * p<.5 versus Ctl, n=7 Figure S3
8 Macrophage Immunostaining With antif4/8 spleen Without antif4/8 D A ICAM 3 Ctl Canr DTgA heart E 3 VCAM 4 CD68 3 F Canr B Canr TNFα,6,,8,4 C Canr MCP 5 * * 4 3 Canr Figure S4
9 Figure S4. Effects of, cardiac MR overexpression and the combination of both on mrna of inflammation markers. (A): Macrophage immunostaining with antif4/8 antibody indicating the absence of macrophage infiltration in heart from controls (Ctl) and DTg (DTgA) mice. Spleen was used as a positive control and incubation without antif4/8 antibody was used to assess nonspecific staining in tissue sections; (B): CD68 mrna abundance is not altered in the various experimental conditons; (C) MCP mrna is induced by only, independently of MR overexpression or MR antagonism. Expression of ICAM (D), VCAM (E) and TNFa (F) are not modified. Open bars: Ctl mice, gray bars: DTg mice. : treatment; Canr: Canrenoate treatment. * p<.5 versus Ctl, p<.5 versus DTg. n=7.
10 A 4 * 3 P47 mrna * Canr B P67 mrna 6 * * 4 Canr D,6 P67 protein,,8,4,6,,8,4 Canr C P47 protein Canr Figure S5
11 Figure S5. Effects of, cardiac MR overexpression and the combination of both on mrna of p47 and p67 subunits. Expression of p47 and p67 mrnas (AC) are increased by but not cardiac MR overexpression, while p47 and p67 proteins (BD) are not altered either by or cardiac MR overexpression. Open bars: Ctl mice, gray bars: DTg mice. : treatment; Canr: Canrenoate treatment. * p<.5 versus Ctl, p<.5 versus DTg. n=7.
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