DIFFERENTIAL EXPRESSION OF SPARC AND THROMBOSPONDIN-1 IN WOUND REPAIR - IMMUNOLOCALIZATION AND IN-SITU HYBRIDIZATION

被引:199
作者
REED, MJ
PUOLAKKAINEN, P
LANE, TF
DICKERSON, D
BORNSTEIN, P
SAGE, EH
机构
[1] UNIV WASHINGTON, DEPT BIOL STRUCT, SM-20, SEATTLE, WA 98195 USA
[2] UNIV WASHINGTON, DEPT MED, SEATTLE, WA 98195 USA
[3] UNIV WASHINGTON, DEPT BIOCHEM, SEATTLE, WA 98195 USA
[4] BRISTOL MYERS SQUIBB, PHARMACEUT RES INST, SEATTLE, WA USA
关键词
EXTRACELLULAR MATRIX; TYPE-I COLLAGEN; DERMIS; INJURY;
D O I
10.1177/41.10.8245406
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
SPARC and thrombospondin 1 (TSP-1) are secreted glycoproteins expressed by similar types of cells in culture and in tissues. To compare these two proteins in vivo, we analyzed the differential expression of SPARC and TSP-1 during wound repair. Full-thickness incision wounds were made in rats and biopsied at 12 hr-14 days. Antibodies against SPARC revealed an increased proportion of immunoreactive fibroblastic cells at the wound edge at 3 days with maximal numbers at 7 days. In situ hybridization for SPARC produced results consistent with those of immunohistochemistry. With combined immunohistochemistry and in situ hybridization, some of the macrophages at the wound edge expressed SPARC mRNA. In contrast, immunoreactivity for TSP-1 was extracellular; expression at the wound edge was noted at 12 hr and was maximal at 1-2 days. TSP-1 mRNA was found in the thrombus, but not at the wound edge. In conclusion, SPARC and TSP-1 have contrasting roles during wound healing. SPARC expression from the middle through late stages of repair was consistent with its previously proposed functions in remodeling; in contrast, the transient expression of TSP-1 early in repair might facilitate the action of other proteins in recruitment and/or proliferation of cells in the healing wound.
引用
收藏
页码:1467 / 1477
页数:11
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