Phagocytosis of fibronectin and collagens type I, III, and V by human gingival and periodontal ligament fibroblasts in vitro.
Phagocytosis of fibronectin and collagens type I, III, and V by human gingival and periodontal ligament fibroblasts in vitro.
复制标题
人牙龈和牙周膜成纤维细胞对纤连蛋白和 I、III 和 V 型胶原的体外吞噬作用。
DOI:
10.1902/jop.2001.72.10.1340
复制
发表时间:
2001
影响因子:
4.3
通讯作者:
W. Beertsen
中科院分区:
文献类型:
--
作者:
M. T. V. D. Pauw;T. V. D. Bos;Vincent Everts;W. Beertsen
BACKGROUND
Electron microscopic studies have suggested that the volume density of collagen-containing vacuoles in fibroblasts is higher in the periodontal ligament (PDL) than in the gingiva. Whether this difference reflects intrinsic differences in phagocytic capacity among the cells in these tissues is not known.
METHODS
PDL and gingival fibroblasts were isolated from subjects and cultured under identical conditions in the presence of fluorescent beads coated with collagen type I, III, or V or fibronectin. Control beads were coated with bovine serum albumin or an enamel matrix protein mixture that does not constitute part of the extracellular matrix of PDL and gingiva. After various time intervals (1 to 24 hours), the percentage of cells that had internalized beads was assessed by flow cytometry. Since alkaline phosphatase activity has been suggested to play a role in collagen phagocytosis, the activity of this enzyme was determined for all cell populations.
RESULTS
The results demonstrated the following order in the percentage of cells internalizing protein-coated beads: fibronectin > collagen type I > III > V. Internalization of collagen type I-coated beads exceeded that of beads coated with bovine serum albumin or enamel matrix proteins by 6 and 3 times, respectively. No differences were observed in collagen phagocytic activity between PDL and gingival fibroblasts, and no relationship could be demonstrated between collagen phagocytosis and alkaline phosphatase activity.
CONCLUSIONS
We conclude that differences in collagen phagocytosis between PDL and gingiva, as observed in vivo, are not likely to be explained in terms of intrinsic phagocytic capacities of these cells.
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影响因子:
4.3
作者:
Cho,MI;Lee,YL;Garant,PR
通讯作者:
Garant,PR
DOI:
10.1006/bbrc.1995.1003
发表时间:
1995-01-05
影响因子:
3.1
作者:
MURRELL, GAC;JANG, D;WILLIAMS, RJ
通讯作者:
WILLIAMS, RJ
DOI:
10.1006/bbrc.1996.0125
发表时间:
1996-01-26
影响因子:
3.1
作者:
Trachtman, H;Futterweit, S;Singhai, PC
通讯作者:
Singhai, PC
影响因子:
3.5
作者:
Pamela S. Howard;Umberto Kucich;Rita Taliwal;Jonathan Korostoff
通讯作者:
Pamela S. Howard;Umberto Kucich;Rita Taliwal;Jonathan Korostoff
影响因子:
20.1
作者:
Ziche, M;Parenti, A;Presta, M
通讯作者:
Presta, M