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DOI: 10.1369/jhc.4A6425.2005
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Journal of Histochemistry and Cytochemistry
Volume 53 (5): 571-581, 2005
Copyright ©The Histochemical Society, Inc.

SPARC-thrombospondin-2-double-null Mice Exhibit Enhanced Cutaneous Wound Healing and Increased Fibrovascular Invasion of Subcutaneous Polyvinyl Alcohol Sponges

Pauli A. Puolakkainen, Amy D. Bradshaw, Rolf A. Brekken, May J. Reed, Themis Kyriakides, Sarah E. Funk, Michel D. Gooden, Robert B. Vernon, Thomas N. Wight, Paul Bornstein and E. Helene Sage

Hope Heart Program, Benaroya Research Institute at Virginia Mason, Seattle, Washington (PAP,ADB,RAB,SEF,MDG,RBV, TNW,EHS); Departments of Medicine (PAP,MJR,PB) and Biochemistry (TK,PB), University of Washington, Seattle, Washington; and Department of Surgery, Helsinki University Central Hospital, Helsinki, Finland (PAP)

Correspondence to: E. Helene Sage, PhD, Hope Heart Program, Benaroya Research Institute at Virginia Mason, 1201 9th Ave., Seattle, WA 98101. E-mail: hsage{at}benaroyaresearch.org or pauli.puolakkainen{at}hus.fi

Secreted protein acidic and rich in cysteine (SPARC) and thrombospondin-2 (TSP-2) are structurally unrelated matricellular proteins that have important roles in cell–extracellular matrix (ECM) interactions and tissue repair. SPARC-null mice exhibit accelerated wound closure, and TSP-2-null mice show an overall enhancement in wound healing. To assess potential compensation of one protein for the other, we examined cutaneous wound healing and fibrovascular invasion of subcutaneous sponges in SPARC-TSP-2 (ST) double-null and wild-type (WT) mice. Epidermal closure of cutaneous wounds was found to occur significantly faster in ST-double-null mice, compared with WT animals: histological analysis of dermal wound repair revealed significantly more mature phases of healing at 1, 4, 7, 10, and 14 days after wounding, and electron microscopy showed disrupted ECM at 14 days in these mice. ST-double-null dermal fibroblasts displayed accelerated migration, relative to WT fibroblasts, in a wounding assay in vitro, as well as enhanced contraction of native collagen gels. Zymography indicated that fibroblasts from ST-double-null mice also produced higher levels of matrix metalloproteinase (MMP)-2. These data are consistent with the increased fibrovascular invasion of subcutaneous sponge implants seen in the double-null mice. The generally accelerated wound healing of ST-double-null mice reflects that described for the single-null animals. Importantly, the absence of both proteins results in elevated MMP-2 levels. SPARC and TSP-2 therefore perform similar functions in the regulation of cutaneous wound healing, but fine-tuning with respect to ECM production and remodeling could account for the enhanced response seen in ST-double-null mice.

(J Histochem Cytochem 53:571–581, 2005)

Key Words: SPARC • thrombospondin • wound healing • matricellular • extracellular matrix • epidermis • dermis • angiogenesis • collagen


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