Yang Hongming, Li Juncong, Wang Yihe, Hu Quan
Department of Burn and Plastic Surgery, First Hospital Affiliated to General Hospital of PLA Beijing 100048, China.
Int J Clin Exp Med. 2015 Feb 15;8(2):2267-72. eCollection 2015.
This study was designed to elucidate the effects of CD14 and TLR4 on the proliferation of LPS-mediated normal human skin fibroblasts and to gain new insights into the mechanisms underlying LPS-induced scar formation.
Cell morphology and density were observed using an inverted microscope. Proliferation curves were described by MTT. The number of proliferating cells was counted by staining the cells with trypan blue. Cells were stained with propidium iodide (PI) and the phase of cell generation cycle was determined by flow cytometry.
The growth rate detected in groups B, C, D was slower compared to group A after 48 h. All proliferation curves were approximately S shaped and the peak was seen on days 6, followed by a sharp decline on days 7. The proliferation rate of groups B, C, D was significantly slower than group A. After the staining, we found a significantly smaller number of proliferating cells in groups B, C, D as compared to group A. Flow cytometry revealed that the ratio of proliferating cells at S phase was lower in the groups B, C, D as compared to group A.
Both separate and combined use of anti-CD14 and anti-TLR4 enable a significant decline in the rate and capacity of proliferation, with the latter pretreatment resulting in the sharpest reduction. Therefore, it seems likely that anti-CD14 along with anti-TLR4 is significantly engaged in the signaling mechanisms of LPS-mediated fibroblast proliferation.
本研究旨在阐明CD14和TLR4对脂多糖(LPS)介导的正常人皮肤成纤维细胞增殖的影响,并深入了解LPS诱导瘢痕形成的潜在机制。
使用倒置显微镜观察细胞形态和密度。用MTT法绘制增殖曲线。用台盼蓝对细胞染色以计数增殖细胞的数量。用碘化丙啶(PI)对细胞染色,通过流式细胞术确定细胞生成周期的阶段。
48小时后,B、C、D组的生长速率比A组慢。所有增殖曲线大致呈S形,在第6天达到峰值,随后在第7天急剧下降。B、C、D组的增殖速率明显低于A组。染色后,我们发现B、C、D组的增殖细胞数量明显少于A组。流式细胞术显示,与A组相比,B、C、D组处于S期的增殖细胞比例较低。
单独或联合使用抗CD14和抗TLR4均可使增殖速率和能力显著下降,后者预处理导致的下降最为明显。因此,抗CD14和抗TLR4似乎在很大程度上参与了LPS介导的成纤维细胞增殖的信号传导机制。