Diabetes-induced fibrotic matrix inhibits intramembranous bone healing

被引:4
|
作者
Khosravi, Roozbeh [1 ]
Trackman, Philip C. [1 ,2 ]
机构
[1] Boston Univ, Henry M Goldman Sch Dent Med, Dept Mol & Cell Biol, Boston, MA 02118 USA
[2] Boston Univ, Henry M Goldman Sch Dent Med, Div Oral Biol, Boston, MA 02118 USA
关键词
Bone; Diabetes; Fibrosis; Lysyl oxidase; Wound healing; OSTEOBLASTIC MC3T3-E1 CELLS; GLYCATION END-PRODUCTS; LYSYL OXIDASE; COLLAGEN; DIFFERENTIATION; INSULITIS; MELLITUS; RECEPTOR; CBFA1;
D O I
10.1007/s12079-014-0242-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Diabetes diminishes bone healing and ossification. Reduced bone formation in intramembranous ossification is known, yet the mechanism(s) behind impaired intramembranous bone healing are unclear. Here we report the formation of a fibrotic matrix during healing of intramembranous calvarial bone defects that appears to exclude new bone growth. Our histological analyses of 7-day and 14-day calvaria bone healing tissue in chemically-induced diabetic mice and non-diabeticmice showed the accumulation of a non-mineralized fibrotic matrix, likely as a consequence of unresolved hematomas under diabetic conditions. Elevated mRNA and enzyme activity levels of lysyl oxidase on day 7 in diabetic bone healing tissues also supports that the formation of a fibrotic matrix occurs in these tissues. Based on these findings, we propose that elevated fibroblast proliferation and formation of a non-mineralized fibrotic extracellular matrix in diabetes contributes to deficient intramembranous bone healing in diabetes. A greater understanding of this process has relevance to managing dental procedures in diabetics in which successful outcomes depend on intramembranous bone formation.
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页码:19 / 26
页数:8
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