Akasaka Yoshikiyo, Ono Ichiro, Yamashita Toshiharu, Jimbow Kowichi, Ishii Toshiharu
Second Department of Pathology, School of Medicine, Toho University, Tokyo, Japan.
J Pathol. 2004 Jun;203(2):710-20. doi: 10.1002/path.1574.
Cytokines are thought to play an important role in cellular loss and apoptosis during the repair of granulation tissue. In order to investigate the role of apoptosis following the administration of basic fibroblast growth factor (bFGF) to a wound, the present study examined the relationship between the degree of granulation tissue formation and the level of apoptosis in rat skin incisional wounds, following treatment with an intradermal injection of bFGF (0.1 microg and 1 microg per cm of wound). Histological assessment of the width of the wound tissue showed that the degree of granulation tissue in the 1 microg-bFGF-treated group had increased by day 7, but then subsequently diminished by days 14 and 28. The TUNEL index increased rapidly from day 1, peaking on day 7, with the index being higher in the 1 microg-bFGF-treated group on days 4, 7, and 14, when compared with a control group. In parallel with a marked increase in the TUNEL index over the first 14 days, the number of cells positive for vimentin and CD3 in the 1 microg-bFGF-treated wounds had decreased by day 14. The number of PCNA-positive cells, an indicator of cell proliferation, peaked on day 4 in the bFGF-treated wounds and then declined rapidly. On the basis of these results, it is suggested that the suppression of granulation tissue formation in bFGF-treated wounds is mainly due to an early and persistent increase in apoptosis in the granulation tissue cells. The expression of both transforming growth factor (TGF)-beta1 and bFGF was also elevated in the bFGF-treated wounds on days 4 and 7, suggesting that fibroblast apoptosis was induced by bFGF treatment. Unexpectedly, on day 28, the wound breaking strength was not reduced in the bFGF-treated wounds. These results indicate that apoptosis regulation following bFGF administration to an incisional wound may lead effectively to granulation tissue formation and promote a scar-less repair process.
细胞因子被认为在肉芽组织修复过程中的细胞丢失和凋亡中起重要作用。为了研究在伤口局部应用碱性成纤维细胞生长因子(bFGF)后凋亡的作用,本研究检测了大鼠皮肤切口伤口经皮内注射bFGF(每厘米伤口0.1微克和1微克)处理后,肉芽组织形成程度与凋亡水平之间的关系。对伤口组织宽度的组织学评估显示,1微克bFGF处理组的肉芽组织程度在第7天时增加,但在第14天和第28天时随后减少。TUNEL指数从第1天开始迅速升高,在第7天达到峰值,在第4天、第7天和第14天时,1微克bFGF处理组的指数高于对照组。与最初14天TUNEL指数的显著增加同时,1微克bFGF处理伤口中波形蛋白和CD3阳性细胞的数量在第14天时减少。PCNA阳性细胞数量作为细胞增殖的指标,在bFGF处理伤口中于第4天达到峰值,然后迅速下降。基于这些结果,提示bFGF处理伤口中肉芽组织形成的抑制主要是由于肉芽组织细胞凋亡的早期和持续增加。在第4天和第7天时,bFGF处理伤口中转化生长因子(TGF)-β1和bFGF的表达也升高,提示bFGF处理诱导了成纤维细胞凋亡。出乎意料的是,在第28天时,bFGF处理伤口的抗张强度并未降低。这些结果表明,在切口伤口局部应用bFGF后对凋亡的调节可能有效地导致肉芽组织形成并促进无瘢痕修复过程。