Bielenberg D R, Bucana C D, Sanchez R, Donawho C K, Kripke M L, Fidler I J
Department of Cell Biology, The University of Texas MD Anderson Cancer Center, Houston 77030, USA.
J Invest Dermatol. 1998 Nov;111(5):864-72. doi: 10.1046/j.1523-1747.1998.00378.x.
We determined whether cutaneous angiogenesis induced by exposure of mice to ultraviolet-B (UVB) radiation is associated with an imbalance between positive and negative angiogenesis-regulating molecules. Unshaved C3H/HeN mice were exposed to a single dose (15 kJ per m2) of UVB. At various times, the mice were killed, and their external ears were processed for routine histology and immunohistochemistry. Antibodies against proliferating cell nuclear antigen and bromodeoxyuridine identified dividing cells. Antibodies against CD31/ PECAM-1 identified endothelial cells, and antibodies against basic fibroblast growth factor (bFGF), vascular endothelial growth factor/vascular permeability factor, and interferon-beta (IFN-beta) identified angiogenesis-regulating molecules. Epidermal hyperplasia was documented by 48 h and reached a maximum on day 7 after exposure to UVB. The expression of bFGF increased by 24 h, whereas the expression of IFN-beta decreased by 72 h after exposure to UVB. The expression of vascular endothelial growth factor/vascular permeability factor increased slightly after irradiation. The altered balance between bFGF and IFN-beta was associated with increased endothelial cell proliferation (bromodeoxyuridine + CD31 + cells) within existing blood vessels, leading to telangiectasia and new blood vessels. UV-induced epidermal hyperplasia and cutaneous angiogenesis were highest in IFN-alpha/beta receptor knockout mice. These results demonstrate that in response to UVB radiation, dividing keratinocytes produce a positive angiogenic molecule (bFGF) but not a negative angiogenic molecule (IFN-beta), and that this altered balance is associated with enhanced cutaneous angiogenesis.
我们确定了小鼠暴露于紫外线B(UVB)辐射所诱导的皮肤血管生成是否与血管生成正负调节分子之间的失衡有关。未剃毛的C3H/HeN小鼠接受单次剂量(每平方米15千焦)的UVB照射。在不同时间点处死小鼠,取其外耳进行常规组织学和免疫组织化学处理。针对增殖细胞核抗原和溴脱氧尿苷的抗体用于识别分裂细胞。针对CD31/血小板内皮细胞黏附分子-1的抗体用于识别内皮细胞,针对碱性成纤维细胞生长因子(bFGF)、血管内皮生长因子/血管通透因子和干扰素-β(IFN-β)的抗体用于识别血管生成调节分子。UVB照射后48小时记录到表皮增生,并在第7天达到最大值。暴露于UVB后24小时,bFGF的表达增加,而IFN-β的表达在72小时后下降。照射后血管内皮生长因子/血管通透因子的表达略有增加。bFGF和IFN-β之间平衡的改变与现有血管内内皮细胞增殖(溴脱氧尿苷+CD31+细胞)增加有关,导致毛细血管扩张和新血管形成。UV诱导的表皮增生和皮肤血管生成在IFN-α/β受体敲除小鼠中最为明显。这些结果表明,响应UVB辐射时,分裂的角质形成细胞产生一种正向血管生成分子(bFGF),但不产生负向血管生成分子(IFN-β),且这种平衡改变与皮肤血管生成增强有关。