Defective valvulogenesis in HB-EGF and TACE-null mice is associated with aberrant BMP signaling
2003; Springer Nature; Volume: 22; Issue: 11 Linguagem: Inglês
10.1093/emboj/cdg264
ISSN1460-2075
Autores Tópico(s)Cardiac Valve Diseases and Treatments
ResumoArticle1 June 2003free access Defective valvulogenesis in HB-EGF and TACE-null mice is associated with aberrant BMP signaling Leslie F. Jackson Leslie F. Jackson Department of Biochemistry & Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA UNC Lineberger Comprehensive Cancer Center, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Search for more papers by this author Ting Hu Qiu Ting Hu Qiu Department of Biochemistry & Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Present address: Advanced Technology Center, National Cancer Institute, Gaithersburg, MD, 20892 USA Search for more papers by this author Susan W. Sunnarborg Susan W. Sunnarborg Department of Biochemistry & Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Search for more papers by this author Aileen Chang Aileen Chang Department of Biochemistry & Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Search for more papers by this author Chunlian Zhang Chunlian Zhang Carolina Cardiovascular Biology Center and Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Search for more papers by this author Cam Patterson Cam Patterson Carolina Cardiovascular Biology Center and Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Search for more papers by this author David C. Lee Corresponding Author David C. Lee Department of Biochemistry & Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA UNC Lineberger Comprehensive Cancer Center, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Search for more papers by this author Leslie F. Jackson Leslie F. Jackson Department of Biochemistry & Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA UNC Lineberger Comprehensive Cancer Center, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Search for more papers by this author Ting Hu Qiu Ting Hu Qiu Department of Biochemistry & Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Present address: Advanced Technology Center, National Cancer Institute, Gaithersburg, MD, 20892 USA Search for more papers by this author Susan W. Sunnarborg Susan W. Sunnarborg Department of Biochemistry & Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Search for more papers by this author Aileen Chang Aileen Chang Department of Biochemistry & Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Search for more papers by this author Chunlian Zhang Chunlian Zhang Carolina Cardiovascular Biology Center and Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Search for more papers by this author Cam Patterson Cam Patterson Carolina Cardiovascular Biology Center and Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Search for more papers by this author David C. Lee Corresponding Author David C. Lee Department of Biochemistry & Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA UNC Lineberger Comprehensive Cancer Center, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA Search for more papers by this author Author Information Leslie F. Jackson1,2, Ting Hu Qiu1,3, Susan W. Sunnarborg1, Aileen Chang1, Chunlian Zhang4, Cam Patterson4 and David C. Lee 1,2 1Department of Biochemistry & Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA 2UNC Lineberger Comprehensive Cancer Center, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA 3Present address: Advanced Technology Center, National Cancer Institute, Gaithersburg, MD, 20892 USA 4Carolina Cardiovascular Biology Center and Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC, 27599 USA *Corresponding author. E-mail: [email protected] The EMBO Journal (2003)22:2704-2716https://doi.org/10.1093/emboj/cdg264 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info Heparin-binding epidermal growth factor (HB-EGF) and betacellulin (BTC) are activating ligands for EGF receptor (EGFR/ErbB1) and ErbB4. To identify their physiological functions, we disrupted mouse HB-EGF and BTC alleles by homologous recombination. Most HB-EGF−/− mice died before weaning, and survivors had enlarged, dysfunctional hearts and reduced lifespans. Although BTC−/− mice were viable and fertile and displayed no overt defects, the lifespan of double null HB-EGF−/−/BTC−/− mice was further reduced, apparently due to accelerated heart failure. HB-EGF−/− newborns had enlarged and malformed semilunar and atrioventricular heart valves, and hypoplastic, poorly differentiated lungs. Defective cardiac valvulogenesis was the result of abnormal mesenchymal cell proliferation during remodeling, and was associated with dramatic increases in activated Smad1/5/8. Consistent with the phenotype, HB-EGF transcripts were localized to endocardial cells lining the margins of wild-type valves. Similarly defective valvulogenesis was observed in newborn mice lacking EGFR and tumor necrosis factor-α converting enzyme (TACE). These results suggest that cardiac valvulogenesis is dependent on EGFR activation by TACE-derived soluble HB-EGF, and that EGFR signaling is required to regulate bone morphogenetic protein signaling in this context. Introduction The epidermal growth factor (EGF)–ErbB signaling network includes multiple polypeptide ligands of the EGF/neuregulin superfamily, and four related tyrosine kinase receptors, epidermal growth factor receptor (EGFR)/ErbB1–ErbB4 (reviewed by Riese and Stern, 1998). EGF-like growth factors share a conserved receptor binding motif and soluble forms are usually derived from bioactive, integral membrane precursors. Besides EGF, they include transforming growth factor α (TGFα), amphiregulin (AR), heparin-binding epidermal growth factor (HB-EGF), betacellulin (BTC), epiregulin and the recently described epigen (Strachan et al., 2001). These proteins all bind to EGFR/ErbB1, inducing receptor dimerization, tyrosine kinase activation and downstream signaling pathways controlling cell proliferation, differentiation, survival or motility. Heparin-binding EGF and BTC can also bind to ErbB4 (Riese et al., 1996a; Elenius et al., 1997). EGF family members vary in their ability to activate distinct ErbB heterodimers, and this may partly account for differences in their bioactivities in cell culture (Beerli and Hynes, 1996; Riese et al., 1996b; Graus-Porta et al., 1997). Numerous actions are ascribed to the EGF family of growth factors, but their physiological functions are not well understood. Hence, our laboratory has derived mice lacking several family members individually or in combination. These studies have revealed specific roles for TGFα in patterning and function of hair follicles and migration of fetal eyelid epidermis (Luetteke et al., 1993), and for AR supported by EGF and TGFα in ductal morphogenesis in the developing mammary gland (Luetteke et al., 1999). Additionally, all three ligands are required for optimal neonatal growth, in part reflecting their roles in the mammary gland, as well as their requirement for normal development and cytoprotection of the gastrointestinal tract (Troyer et al., 2001). In contrast, EGFR−/− mice usually die in utero, although the timing is markedly affected by the genetic background (Miettinen et al., 1995; Sibilia and Wagner, 1995; Threadgill et al., 1995). However, more recent tetraploid aggregation experiments have allowed development to term (Sibilia et al., 1998). In comparison, the restricted or mild phenotypes of EGF family knockouts indicate that there is considerable redundancy or cooperativity in the action of these ErbB ligands. Here we report the inactivation of mouse HB-EGF and BTC. HB-EGF was first identified as a heparin-binding mitogen for fibroblasts and smooth muscle cells that was secreted by human macrophages (Besner et al., 1990; Higashiyama et al., 1991). It is widely distributed in mammalian tissues, including skin, lung and heart (reviewed by Raab and Klagsbrun, 1997). Induced at sites of wounding, HB-EGF may also function in response to vascular injury since it is expressed in atherosclerotic plaques by aortic smooth muscle cells and other cell types (Raab and Klagsbrun, 1997), and its production by endothelial cells is induced by VEGF (Arkonac et al., 1998) and TNFα (Yoshizumi et al., 1992). Heparin-binding EGF is also implicated in uterine growth and blastocyst implantation (Kennedy et al., 1993; Das et al., 1994). Heparin-binding EGF is derived from a bioactive, transmembrane precursor, proHB-EGF, which also functions as the diphtheria toxin receptor in primates (Naglich et al., 1992). ProHB-EGF interacts with tetraspanin and other membrane proteins, and may distinctively signal growth inhibition or apoptosis rather than the proliferative response induced by soluble HB-EGF (reviewed by Iwamoto and Mekada, 2000). In this light, the identity of the protease that regulates HB-EGF shedding is an important topic that has assumed additional significance because regulated release of soluble HB-EGF contributes to transactivation of EGFR by G-protein-coupled receptors (GPCR) (Prenzel et al., 1999). Several metalloproteases, including members of the A Disintegrin and Metalloprotease (ADAM) (Izumi et al., 1998; Asakura et al., 2002; Lemjabbar and Basbaum, 2002; Yan et al., 2002) and matrix metalloprotease (MMP) (Suzuki et al., 1997; Bursi et al., 2002; Yu et al., 2002) families, have been identified as putative proHB-EGF convertases. BTC was identified as a mitogen secreted by pancreatic β-cell insulinomas (Sasada et al., 1993; Shing et al., 1993) and it is implicated in the normal development and function of the pancreas (reviewed in Dunbar and Goddard, 2000). It is highly expressed in fetal pancreas, promotes islet growth (Demeterco et al., 2000) and co-regulates differentiation of insulin-producing cells (Mashima et al., 1996, 1999). It also promotes β-cell neogenesis and improves glucose tolerance in a mouse model of diabetes (Yamamoto et al., 2000). However, BTC is also widely expressed and additional roles in blastocyst implantation (Das et al., 1997), gastrointestinal function (Kallincos et al., 2000) and atherosclerosis (Tamura et al., 2001) have been proposed. We report here that HB-EGF−/− and BTC−/− mice are viable and fertile, but HB-EGF−/− mice have severely shortened lifespans and exhibit specific cardiac and lung defects. These phenotypes are mimicked in mice lacking either EGFR or tumor necrosis factor-α converting enzyme (TACE), providing genetic evidence that these proteins are the relevant ErbB receptor and HB-EGF convertase, respectively. Results HB-EGF−/− and BTC−/− mice are viable and fertile Mouse HB-EGF and BTC were disrupted in embryonic stem cells by homologous recombination (Figure 1A). HB-EGF exons 1 and 2 were replaced with PGK-Neo, thus deleting the signal peptide and propeptide, and simultaneously inducing a frameshift to prevent translational read through. BTC was inactivated by eliminating exon 3, which encodes the first two loops of the EGF-like sequence that are critical for receptor binding. Lines of HB-EGF−/− and BTC−/− mice were established from targeted ES clones on a mixed C57BL/6J × 129 background, and the desired targeting events verified by Southern blots of genomic DNA (Figure 1B) and exon-specific PCR (Figure 1C). Northern blots confirmed the absence of the respective transcripts (Figure 1D). Figure 1.Targeted disruption of HB-EGF and BTC. (A) Schematics illustrate strategies used to inactivate the mouse HB-EGF and BTC alleles. Targeting constructs were designed to eliminate exons (filled boxes) 1 and 2 of the HB-EGF gene, or exon 3 of the BTC gene using genomic sequences isolated from a mouse 129/Sv library. Heavy lines denote 5′ and 3′ arms of homology, and dashed lines bracket the genomic regions replaced by the Neo cassette. Hatched boxes mark probes used to verify correct targeting, and the locations of useful restriction sites and resulting fragments are noted. B, BglII; E, EcoRI; H, HindIII; N, NcoI; Nt, NotI; S, StuI. (B) Southern blot analyses of genomic DNAs digested with NcoI, showing results diagnostic for wild-type, heterozygous and homozygous targeted alleles using the indicated probes. (C) Genomic PCR using exon- or Neo-specific primers. (D) Northern blots of lung RNA from mice of the designated genotypes. Arrows indicate the apparent mass of DNA or RNA species. Ntds, nucleotides; kb, kilobases. Download figure Download PowerPoint The average litter size from intercrosses of HB-EGF+/− mice was 10.2 (n = 13 litters, 132 pups), a typical size for our colony. However, 12 neonates died in the first week after birth and genotyping of the remaining 120 pups at weaning revealed a non-Mendelian distribution of genotypes: 28%+/+, 62%+/− and 11%−/−. Surviving HB-EGF−/− mice grew normally, were fertile and matings between them produced litters of typical size at birth, suggesting there was little to no intrauterine loss of HB-EGF−/− mice. However, only 40% of the HB-EGF−/− offspring survived to weaning (n = 7 litters, 20/50 pups survived) compared with >80% of control pups (n = 5 litters, 32/39 pups survived), reminiscent of the results of HB-EGF+/− matings. Mammary gland morphology was normal in HB-EGF−/− dams, and there was no functional evidence of impaired lactation. Gastrointestinal tract architecture was also normal in HB-EGF−/− neonates, and the body weights of surviving HB-EGF−/− pups were within normal range from 1 to 3 weeks of age (data not shown). Thus, increased mortality of HB-EGF−/− mice was not ascribed to defects in nursing or nutrient absorption. Matings between BTC+/− parents produced offspring in the expected Mendelian ratios (18%+/+, 56%+/−, 26%−/−; n = 14 litters) at weaning and BTC−/− mice were viable and grew normally. Matings between homozygous BTC−/− mice also yielded normal sized litters. Since BTC is implicated in the growth and development of the pancreas (Dunbar and Goddard, 2000), we specifically examined this tissue. No morphological differences were observed in newborn pancreata, and adult BTC+/+ and BTC−/− males responded similarly to a glucose challenge test (data not shown). Also, expression of insulin, glucagon, cytokeratin and amylase were normal in BTC−/− pancreata (P.Miettinen, personal communication). Defective cardiac valvulogenesis in HB-EGF−/− mice Examination of newborn hearts revealed grossly enlarged and stenotic semilunar (SL) (aortic and pulmonary) and atrioventricular (AV) valves in all newborn HB-EGF−/− mice (n = 14) compared with HB-EGF+/+ mice (n = 10) (Figure 2A–F). For example, the mean area of HB-EGF−/− aortic valves (Figure 2M) was 56.7 ± 17 mm2 (n = 7) compared with 21.9 ± 4.6 mm2 (n = 5) for HB-EGF+/+ controls (P = 0.0025). Figure 2.Similarly defective cardiac valves in HB-EGF−/−, EGFR−/− and TACE−/− mice. (A–L) H&E sections of newborn (P1) hearts of the indicated genotypes showing atrioventricular (AV) and semilunar valves (arrows). Scale bar = 500 μm. (M) Measurement of aortic valve areas (mm2) ± SD of the indicated P1 mutant hearts, including those of rescued ErbB4−/− mice, with their respective +/+ controls. Asterisks denote statistically significant results. Download figure Download PowerPoint Enlarged SL, but not AV, valves were observed in waved-2 (EGFRwa-2/wa-2) mice, which encode a kinase-impaired EGFR mutant, and in EGFR−/− mice (Chen et al., 2000). We examined EGFRwa-2/wa-2 hearts and confirmed that only SL valves were enlarged (data not shown). However, both SL and AV valves were dramatically enlarged in EGFR−/− hearts (Figure 2G–I). Thus, aortic valve area in four EGFR−/− hearts was 56.6 ± 15.4 mm2 compared with 16.7 ± 4.5 mm2 in four control hearts (P = 0.0286) (Figure 2M). We attribute the difference between the two models to residual signaling by the wa-2 receptor and a lower threshold requirement in SL valves. Abnormal valves were not observed in triple null mice lacking AR, EGF and TGFα (Chen et al., 2000), nor in BTC−/− hearts (data not shown). Collectively, these results indicate that HB-EGF is uniquely required as an EGFR ligand for cardiac valvulogenesis. TACE−/− mice display identical heart valve defects ADAM17/TACE is required for conversion of membrane-anchored proTGFα to the soluble ligand (Peschon et al., 1998; Sunnarborg et al., 2002). TACE−/− mice displayed generalized epithelial defects reminiscent of those observed in EGFR−/− animals, and we showed in cell-based and in vitro peptide assays that TACE promotes HB-EGF processing (Sunnarborg et al., 2002). To assess whether TACE functions as an HB-EGF convertase in vivo, we examined the heart valves of newborn TACE-null mice. Hearts from these mice had SL and AV valves that were similarly enlarged compared with HB-EGF−/− and EGFR−/− counterparts (Figure 2J–L), e.g. the mean area of TACE−/− aortic valves was 57.5 ± 29.4 mm2 compared with 20.0 ± 7.4 mm2 for TACE+/+ controls (n = 4 each genotype; P = 0.0079) (Figure 2M). Highly localized expression of HB-EGF in valves We examined HB-EGF expression in control hearts during cardiac valve development, from E11.5 through E15.5. HB-EGF transcripts were highly localized to the endocardial cells lining the margins of AV and SL (both aortic and pulmonary) valves, as shown at E14.5 (Figure 3A–F). Diffuse expression was also apparent throughout the myocardium, especially at later times (data not shown). EGFR transcripts were detected throughout the heart, including in developing valves, but enriched in the endocardial cushion, as shown for E14.5 (Figure 3G and H). TACE transcripts were found throughout the heart at this same developmental stage (Figure 3M and N), including in HB-EGF-expressing cells at the margins of AV and SL valves. Immuno histochemistry confirmed broad distribution of TACE protein (data not shown). Thus, growth factor, receptor and convertase are all coexpressed, consistent with the phenotypic similarities. Figure 3.In situ detection of HB-EGF, EGFR, ErbB3, ErbB4 and TACE transcripts in wild-type cardiac valves. (A–F) HB-EGF; (G and H) EGFR; (I and J) ErbB3; (K and L) ErbB4; (M and N) TACE. Arrows mark regions of high expression. Sense riboprobes were hybridized to confirm specific hybridization in each case (data not shown). AoV, aortic valve; bf, bright field; df, dark field; v, valves. Scale bars = 100 μm. Download figure Download PowerPoint Since HB-EGF binds to ErbB4 as well as EGFR, we considered that ErbB4 might transduce HB-EGF signals required for valvulogenesis. ErbB4 transcripts were detected throughout the developing heart, including in cushions and valves, as shown at E14.5 in Figure 3K and L. This contrasts with restricted expression in the ventricular myocardium at E10.5 (Gassmann et al., 1995). Since ErbB4−/− embryos die early in gestation with defects in ventricular trabeculation, it was not possible to examine valvulogenesis in these mice. However, the knockout has recently been rescued by introduction of an ErbB4 transgene in heart muscle under the control of the α-myosin heavy chain promoter, which directs expression specifically to cardiomyocytes (Tidcombe et al., 2001). We examined SL and AV valves in these transgenic mice and found them to be of normal size (Figure 2M), suggesting that ErbB4 is not required for valvulogenesis. However, we cannot exclude possible low level expression of the transgene in valve mesenchyme sufficient to direct normal valvulogenesis. We also observed ErbB3 transcripts in the cushions and valves from E12.5 to 15.5 (Figure 3I and J), as previously shown for earlier time points (Meyer and Birchmeier, 1995). Thus, ErbB3 could potentially influence HB-EGF signaling through heterodimerization with EGFR. Remodeling of valves requires HB-EGF To address the mechanism of HB-EGF action, we compared valve development in HB-EGF−/− and HB-EGF+/+ hearts from E12.5 to E15.5. Immature valves (AV and PV) were comparably sized at E12.5 and E13.5 in both genotypes, indicating that early events in valve formation occurred normally without HB-EGF. However, subsequent remodeling of valves was clearly perturbed. Whereas large, immature AV (Figure 4A and B) and PV (Figure 4E and F) valves of control hearts were remodeled to form slender valve leaflets, HB-EGF−/− valves remained enlarged throughout the period (Figure 4C, D, G and H). The largest size reduction for HB-EGF+/+ AV valves occurred from E13.5 to E14.5, and for PV valves from E12.5 to E13.5 (Figure 4Q and R). In contrast, HB-EGF−/− valves were only modestly reduced in size, remaining 36–46% larger than the control counterparts through E15.5, differences that were significant (P = 0.0286) for AV valves at both time points and for PV valves at E15.5. Figure 4.Defective remodeling of cardiac valves in mutant mouse hearts. (A–H) H&E sections of HB-EGF+/+ or HB-EGF−/− hearts showing (A–D) atrioventricular (AV) valves or (E–H) pulmonary valves (PV) at the indicated time points. (I–P) H&E sections of heart showing AV valves or PV valves of the indicated TACE or EGFR genotypes at E15.5. Arrows denote valves. Scale bars = 100 μm. (Q–T) Quantitative comparison of valvulogenesis in HB-EGF+/+ or HB-EGF−/− hearts. (Q and R) Cushion/heart ratio ± SD at the indicated ages. (S) Percentage of TUNEL-positive cells at the indicated ages in AV valves or PV; (T) percentage of BrdU-positive cells. Filled bars, HB-EGF+/+; unfilled bars, HB-EGF−/−. Asterisks denote statistically significant results. Download figure Download PowerPoint Impaired remodeling of HB-EGF−/− valves could be due to reduced cellular apoptosis or increased cellular proliferation. TUNEL assays revealed no differences in the percentage of cells undergoing apoptosis in HB-EGF+/+ versus HB-EGF−/− valves at E14.5 or E15.5 (Figure 4S). In contrast, the percentages of bromodeoxyuridine (BrdU)-positive cells were significantly (P = 0.0286) increased ∼3.5-fold in AV valves and ∼2-fold in PV valves of HB-EGF−/− hearts at E14.5 (Figure 4T). There was no change in the distribution of BrdU-positive cells in HB-EGF−/− valves, which were found throughout the valve mesenchyme. Thus, surprisingly, impaired remodeling of HB-EGF−/− valves was due to excessive proliferation of mesenchymal cells. Since the cardiac valves of young HB-EGF−/− adults were even larger and more disfigured than comparable controls (data not shown), we speculate that cellular proliferation continues beyond the embryonic time points analyzed here. To determine whether the enlarged cardiac valves of newborn EGFR−/− and TACE−/− mice had a similar origin, we examined the respective hearts at E15.5. For both genotypes, AV and PV valves were significantly enlarged compared with controls, suggesting that impaired remodeling was also the cause of valve enlargement in these mutants (Figure 4I–P). Bone morphogenetic protein (BMP) signaling is disregulated in the absence of HB-EGF A clue to the mechanism of defective valvulogenesis came from an initial gene array comparison performed with total E14.5 HB-EGF+/+ and HB-EGF−/− hearts. The three genes most strongly upregulated in mutant heart, dHAND, Smad6 and Id-1 (data not shown), are all implicated in BMP signaling, which is required for outflow tract septation and valve development (Kim et al., 2001; Gaussin et al., 2002; Delot et al., 2003). Since Smad6−/− mice have hyperplastic valves (Galvin et al., 2000) similar to those observed here, presumably due to disregulated BMP signaling in the absence of this inhibitor Smad, and cell culture studies have established the potential for EGFR inhibition of BMP signaling (Kretzschmar et al., 1997; Nonaka et al., 1999), we speculated that defective valvulogenesis in our mice could be due to loss of BMP regulation. To test this, we examined activation of Smad1/5/8 in sections of HB-EGF+/+ and HB-EGF−/− hearts using an antibody that detects phosphorylated forms of these BMP signaling effectors. Figure 5 reveals dramatically higher numbers of cells staining positive for nuclear phospho-Smad1/5/8 in pulmonary and aortic valves of mutant hearts compared with the control tissues at E14.5. A similar, albeit less dramatic, trend was seen in AV valves (data not shown). In contrast, HB-EGF+/+ and HB-EGF−/− valves showed similarly high levels of activated Smad1/5/8 in AV and aortic valves at E12.5 during the proliferative phase of valve development (data not shown). Figure 5.Disregulated Smad signaling in HB-EGF mutant cushions. Sections of (A and B) pulmonary valve (PV) or (C and D) aortic valve (AoV) from E14.5 immunostained with phospho-Smad1/5/8 antibody and counterstained with hematoxylin. Arrows mark positive staining cells. Scale bar = 100 μM. Download figure Download PowerPoint HB-EGF−/− hearts are enlarged and dysfunctional An unusually high proportion (43%) of HB-EGF−/− adult males and females died within the first year of life. At necropsy, these mice were found to have enlarged hearts and congested lungs, with no other apparent pathological defects. A systematic comparison showed that the heart-to-body weight ratios of male HB-EGF−/− mice increased continuously from birth through 6 months of age compared with wild-type controls, although the largest relative increase occurred between 3 and 6 weeks of age (data not shown). Examples of enlarged hearts of apparently healthy, 6-week-old male HB-EGF−/− mice are shown in Figure 6A–C. The mean heart-to-body weight ratio for 6-week-old HB-EGF−/− mice was 1.27 ± 0.20% compared with 0.80 ± 0.03% for HB-EGF+/+ controls (n = 5 both genotypes; P = 0.0079). At this stage, ventricular myocyte size (Figure 6D and E) and number per unit area were not significantly different between the two genotypes, indicating that enlargement was due to hypercellularity. However, we did not observe significant incorporation of BrdU into 5-week-old hearts of either genotype, suggesting that proliferation occurred gradually. A comparison of transverse sections from 6-month-old male mice indicated that further heart enlargement included a significant hypertrophic component. Figure 6.Cardiac defects in HB-EGF−/− and HB-EGF−/−/BTC−/− mice. (A) Hearts from 6-week-old male mice. (B and C) H&E-stained cross- sections of 6-week-old (B) HB-EGF+/+ and (C) HB-EGF−/− hearts. (D and E) PAS-stained transverse sections of left ventricle cardiomyocytes. (F) PAS-stained section of thickened aortic valve leaflet from 6-month-old HB-EGF−/− heart. White arrow marks chondrocytes; black arrows denote ectopic cartilage formation. (G) H&E-stained section of HB-EGF−/−/BTC−/− heart. Arrow marks a thrombus in the left atrium. (H and I) Masson trichrome-stained sections of HB-EGF−/−/BTC−/− hearts. Arrows mark extensive intraventricular (H) or focal epicardial (I) fibrosis (blue stain) within or on the left ventricle. v, ventricle; ao, aorta; lv, left ventricle. Scale bars = 3.5 mm (A), 1 mm (B and C), 20 μm (D and E), 100 μm (F), 1 mm (G–I). Download figure Download PowerPoint To assess the functionality of HB-EGF−/− hearts, we performed non-invasive transthoracic echocardiography (ECG) on 5-month-old mice. Left ventricular end-diastolic and -systolic dimensions were significantly larger, confirming cardiomegaly (Table I). Calculations of fractional shortening (SF%) revealed significant systolic dysfunction in HB-EGF−/− mice, which may be observed in advanced human aortic valve disease (although a myopathic contribution to the ECG observations cannot be excluded). Aortic dilation, a classic symptom of valvular stenosis, was also observed in ECGs (data not shown). Table 1. Echocardiogram results for HB-EGF and HB-EGF/BTC mice Genotype BW (g) HR (b.p.m.) IVST (mm) LVEDD (mm) LVESD (mm) PWT (mm) SF (%) HB-EGF+/+ 38.4 ± 3.9 659 ± 55 0.08 ± 0.03 0.32 ± 0.03 0.10 ± 0.02 0.1 ± 0.01 68.7 ± 2.7 HB-EGF−/− 35.3 ± 2.3 668 ± 21 0.10 ± 0.03 0.41 ± 0.05* 0.20 ± 0.05* 0.1 ± 0.02 51.6 ± 7.4* HB-EGF+/+/BTC+/+ 33.6 ± 2.8 653 ± 55 0.07 ± 0.01 0.30 ± 0.02 0.08 ± 0.01 0.07 ± 0.01 71.8 ± 3.3 HB-EGF−/−/BTC−/− 29.0 ± 2.5* 695 ± 43 0.07 ± 0.01 0.39 ± 0.08* 0.17 ± 0.10* 0.09 ± 0.01 58.8 ± 15.9* Non-invasive transthoracic echocardiography was performed on unanesthetized, male mice. Values are mean ± SD for 5-month-old HB-EGF+/+ (n = 5) and HB-EGF−/− (n = 5) mice, and 4-month-old HB-EGF+/+/BTC+/+ (n = 6) and HB-EGF−/−/BTC−/− (n = 6) mice. BW, body weight; HR, heart rate; IVST, interventricular septal distance; LVEDD, left ventricular end-diastolic dimension; LVESD, left ventricular end-systolic dimension; PWT, posterior wall thickness; SF, fractional shortening. Asterisks denote values significantly different from respective wild-type controls (P < 0.05). Histological sections of hearts from similarly aged HB-EGF−/− mice showed grossly enlarged and deformed valves, and confirmed aortic dilation. Chondrocytes and ectopic cartilage formation were observed throughout the aortic valve leaflets of HB-EGF−/− but not control hearts (Figure 6F), possibly as a consequence of disregulated BMP signaling in HB-EGF−/− hearts. Cartilaginous metaplasia and ossification withi
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