Davidovitch Z, Montgomery P C, Yost R W, Shanfeld J L
Anat Rec. 1978 Nov;192(3):351-61. doi: 10.1002/ar.1091920303.
Cyclic AMP and cyclic GMP, considered to be cell proliferation regulators, have been reported to fluctuate in proliferating fibroblasts in vitro. The objectives of this experiment were to study the localization, distribution and staining patterns of these cyclic nucleotides in mechanically-stressed, proliferating periodontal fibroblasts in vivo. Cat canines were tipped by force applications for 0 to 48 hours and serial sagittal sections of fresh frozen, unfixed, undecalcified jaws were processed immuno-histochemically for the localization of cAMP and cGMP. Periodontal tension sites were studied microscopically. Fibroblastic staining for cAMP, which was localized mainly in the cell periphery, did not change appreciably as a result of tension. However, staining intensity increased one hour after the application of force, decreased after 6 hours and increased again at 24 hours. Staining for cGMP, initially covering the entire cell area, was concentrated over nuclei three hours after onset of tension, and diffused over cell periphery and cytoplasm thereafter. Intensity of staining for cGMP was maximal at 3 hours and low at 12 and 48 hours. These results demonstrate that stress-induced fibroblastic responses in vivo involve alterations in staining intensity for both cyclic nucleotides which may correspond with fluctuations of these regulators, reported to occur in vitro in various stages of the mitotic cycle. Moreover, this technique enables the identification of the involved cells in a stimulated, non-synchronized cell population.
环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)被认为是细胞增殖调节剂,据报道它们在体外增殖的成纤维细胞中会发生波动。本实验的目的是研究这些环核苷酸在体内机械应激、增殖的牙周成纤维细胞中的定位、分布和染色模式。对猫的犬齿施加力量0至48小时,对新鲜冷冻、未固定、未脱钙的颌骨连续矢状切片进行免疫组织化学处理,以定位cAMP和cGMP。对牙周张力部位进行显微镜研究。cAMP的成纤维细胞染色主要位于细胞周边,张力作用后无明显变化。然而,施加力量1小时后染色强度增加,6小时后降低,24小时后再次增加。cGMP的染色最初覆盖整个细胞区域,张力开始3小时后集中在细胞核上,此后扩散到细胞周边和细胞质。cGMP的染色强度在3小时时最大,在12小时和48小时时较低。这些结果表明,体内应激诱导的成纤维细胞反应涉及两种环核苷酸染色强度的改变,这可能与这些调节剂在体外有丝分裂周期不同阶段发生的波动相对应。此外,该技术能够在受刺激的、非同步的细胞群体中识别出相关细胞。