Increased ADAMTS1 mediates SPARC-dependent collagen deposition in the aging myocardium

Hiroe Toba, Lisandra E. de Castro Brás, Catalin F. Baicu, Michael R. Zile, Merry L Lindsey, Amy D. Bradshaw

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

Secreted protein acidic and rich in cysteine (SPARC) is a collagen-binding matricellular protein highly expressed during fibrosis. Fibrosis is a prominent component of cardiac aging that reduces myocardial elasticity. Previously, we reported that SPARC deletion attenuated myocardial stiffness and collagen deposition in aged mice. To investigate the mechanisms by which SPARC promotes age-related cardiac fibrosis, we evaluated six groups of mice (n = 5–6/group): young (3–5 mo old), middle-aged (10–12 mo old), and old (18–29 mo old) C57BL/6 wild type (WT) and SPARC-null (Null) mice. Collagen content, determined by picrosirius red staining, increased in an age-dependent manner in WT but not in Null mice. A disintegrin and metalloproteinase with thrombospondin- like motifs 1 (ADAMTS1) increased in middle-aged and old WT compared with young, whereas in Null mice only old animals showed increased ADAMTS1 expression. Versican, a substrate of ADAMTS1, decreased with age only in WT. To assess the mechanisms of SPARC-induced collagen deposition, we stimulated cardiac fibroblasts with SPARC. SPARC treatment increased secretion of collagen I and ADAMTS1 (both the 110-kDa latent and 87-kDa active forms) into the conditioned media as well as the cellular expression of transforming growth factor-β1-induced protein (Tgfbi) and phosphorylated Smad2. An ADAMTS1 blocking antibody suppressed the SPARC-induced collagen I secretion, indicating that SPARC promoted collagen production directly through ADAMTS1 interaction. In conclusion, ADAMTS1 is an important mediator of SPARC-regulated cardiac aging.

Original languageEnglish (US)
Pages (from-to)E1027-E1035
JournalAmerican Journal of Physiology - Endocrinology and Metabolism
Volume310
Issue number11
DOIs
StatePublished - Jun 1 2016
Externally publishedYes

Fingerprint

Thrombospondins
Disintegrins
Metalloproteases
Cysteine
Myocardium
Collagen
Proteins
Fibrosis
Versicans
Blocking Antibodies
Elasticity
Transforming Growth Factors
Conditioned Culture Medium
Carrier Proteins
Fibroblasts

Keywords

  • A disintegrin and metalloproteinase with thrombospondin-like motifs 1
  • Fibroblast
  • Heart
  • Matrix metalloproteinase
  • Secreted protein acidic and rich in cysteine

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Physiology
  • Physiology (medical)

Cite this

Increased ADAMTS1 mediates SPARC-dependent collagen deposition in the aging myocardium. / Toba, Hiroe; de Castro Brás, Lisandra E.; Baicu, Catalin F.; Zile, Michael R.; Lindsey, Merry L; Bradshaw, Amy D.

In: American Journal of Physiology - Endocrinology and Metabolism, Vol. 310, No. 11, 01.06.2016, p. E1027-E1035.

Research output: Contribution to journalArticle

Toba, Hiroe ; de Castro Brás, Lisandra E. ; Baicu, Catalin F. ; Zile, Michael R. ; Lindsey, Merry L ; Bradshaw, Amy D. / Increased ADAMTS1 mediates SPARC-dependent collagen deposition in the aging myocardium. In: American Journal of Physiology - Endocrinology and Metabolism. 2016 ; Vol. 310, No. 11. pp. E1027-E1035.
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abstract = "Secreted protein acidic and rich in cysteine (SPARC) is a collagen-binding matricellular protein highly expressed during fibrosis. Fibrosis is a prominent component of cardiac aging that reduces myocardial elasticity. Previously, we reported that SPARC deletion attenuated myocardial stiffness and collagen deposition in aged mice. To investigate the mechanisms by which SPARC promotes age-related cardiac fibrosis, we evaluated six groups of mice (n = 5–6/group): young (3–5 mo old), middle-aged (10–12 mo old), and old (18–29 mo old) C57BL/6 wild type (WT) and SPARC-null (Null) mice. Collagen content, determined by picrosirius red staining, increased in an age-dependent manner in WT but not in Null mice. A disintegrin and metalloproteinase with thrombospondin- like motifs 1 (ADAMTS1) increased in middle-aged and old WT compared with young, whereas in Null mice only old animals showed increased ADAMTS1 expression. Versican, a substrate of ADAMTS1, decreased with age only in WT. To assess the mechanisms of SPARC-induced collagen deposition, we stimulated cardiac fibroblasts with SPARC. SPARC treatment increased secretion of collagen I and ADAMTS1 (both the 110-kDa latent and 87-kDa active forms) into the conditioned media as well as the cellular expression of transforming growth factor-β1-induced protein (Tgfbi) and phosphorylated Smad2. An ADAMTS1 blocking antibody suppressed the SPARC-induced collagen I secretion, indicating that SPARC promoted collagen production directly through ADAMTS1 interaction. In conclusion, ADAMTS1 is an important mediator of SPARC-regulated cardiac aging.",
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AU - Toba, Hiroe

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AU - Zile, Michael R.

AU - Lindsey, Merry L

AU - Bradshaw, Amy D.

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AB - Secreted protein acidic and rich in cysteine (SPARC) is a collagen-binding matricellular protein highly expressed during fibrosis. Fibrosis is a prominent component of cardiac aging that reduces myocardial elasticity. Previously, we reported that SPARC deletion attenuated myocardial stiffness and collagen deposition in aged mice. To investigate the mechanisms by which SPARC promotes age-related cardiac fibrosis, we evaluated six groups of mice (n = 5–6/group): young (3–5 mo old), middle-aged (10–12 mo old), and old (18–29 mo old) C57BL/6 wild type (WT) and SPARC-null (Null) mice. Collagen content, determined by picrosirius red staining, increased in an age-dependent manner in WT but not in Null mice. A disintegrin and metalloproteinase with thrombospondin- like motifs 1 (ADAMTS1) increased in middle-aged and old WT compared with young, whereas in Null mice only old animals showed increased ADAMTS1 expression. Versican, a substrate of ADAMTS1, decreased with age only in WT. To assess the mechanisms of SPARC-induced collagen deposition, we stimulated cardiac fibroblasts with SPARC. SPARC treatment increased secretion of collagen I and ADAMTS1 (both the 110-kDa latent and 87-kDa active forms) into the conditioned media as well as the cellular expression of transforming growth factor-β1-induced protein (Tgfbi) and phosphorylated Smad2. An ADAMTS1 blocking antibody suppressed the SPARC-induced collagen I secretion, indicating that SPARC promoted collagen production directly through ADAMTS1 interaction. In conclusion, ADAMTS1 is an important mediator of SPARC-regulated cardiac aging.

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