Tanigawa T, Ahluwalia A, Watanabe T, Arakawa T, Tarnawski A S
Department of Medicine, Long Beach Veterans Affairs Healthcare System, Long Beach, California and the University of California-Irvine, CA, USA.
Department of Gastroenterology, Osaka City University Graduate School of Medicine, Osaka, Japan.
J Physiol Pharmacol. 2015 Aug;66(4):617-21.
A previous study has demonstrated that locally administered growth factors such as epidermal growth factor, basic fibroblast growth factor and hepatocyte growth factor can accelerate healing of experimental gastric ulcers in rats. That study indicates that locally administered growth factors can exert potent biological effects resulting in enhanced gastric ulcers healing. However, the fate of injected growth factors, their retention and localization to specific cellular compartments have not been examined. In our preliminary study, we demonstrated that local injection of nerve growth factor to the base of experimental gastric ulcers dramatically accelerates ulcer healing, increases angiogenesis - new blood vessel formation, and improves the quality of vascular and epithelial regeneration. Before embarking on larger, definitive and time sequence studies, we wished to determine whether locally injected nerve growth factor is retained in gastric ulcer's tissues and taken up by specific cells during gastric ulcer healing. Gastric ulcers were induced in anesthetized rats by local application of acetic acid using standard methods; and, 60 min later fluorescein isothiocyanate-labeled nerve growth factor was injected locally to the ulcer base. Rats were euthanized 2, 5 and 10 days later. Gastric specimens were obtained and processed for histology. Unstained paraffin sections were examined under a fluorescence microscope, and the incorporation of fluorescein isothiocyanate-labeled nerve growth factor into various gastric tissue cells was determined and quantified. In addition, we performed immunostaining for S100β protein that is expressed in neural components. Five and ten days after ulcer induction labeled nerve growth factor (injected to the gastric ulcer base) was incorporated into endothelial cells of blood vessels, neuronal, glial and epithelial cells, myofibroblasts and muscle cells. This study demonstrates for the first time that during gastric ulcer healing locally administered exogenous nerve growth factor is retained in gastric tissue and is taken up by endothelial, neural, muscle and epithelial cells. This is likely the basis for the therapeutic action of locally administered nerve growth factor and its stimulation of angiogenesis, tissue regeneration and gastric ulcer healing.
先前的一项研究表明,局部施用的生长因子,如表皮生长因子、碱性成纤维细胞生长因子和肝细胞生长因子,可加速大鼠实验性胃溃疡溃疡愈合。该研究表明,局部施用生长因子可发挥强大的生物学效应,从而促进胃溃疡愈合。然而,注射的生长因子的去向、它们在特定细胞区室中的保留和定位尚未得到研究。在我们的初步研究中,我们证明向实验性胃溃疡底部局部注射神经生长因子可显著加速溃疡愈合、增加血管生成——新血管形成,并改善血管和上皮再生的质量。在开展更大规模、确定性和时间序列研究之前,我们希望确定局部注射的神经生长因子在胃溃疡愈合过程中是否保留在胃组织中,并被特定细胞摄取。采用标准方法通过局部应用乙酸在麻醉大鼠中诱导胃溃疡;60分钟后,将异硫氰酸荧光素标记的神经生长因子局部注射到溃疡底部。2、5和10天后对大鼠实施安乐死。获取胃标本并进行组织学处理。在荧光显微镜下检查未染色的石蜡切片,并确定和量化异硫氰酸荧光素标记的神经生长因子在各种胃组织细胞中的掺入情况。此外,我们对在神经成分中表达的S100β蛋白进行了免疫染色。溃疡诱导后5天和10天,标记的神经生长因子(注射到胃溃疡底部)被血管内皮细胞、神经元、神经胶质和上皮细胞、肌成纤维细胞和肌肉细胞摄取。这项研究首次证明,在胃溃疡愈合过程中,局部施用的外源性神经生长因子保留在胃组织中,并被内皮细胞、神经细胞、肌肉细胞和上皮细胞摄取。这可能是局部施用神经生长因子的治疗作用及其对血管生成、组织再生和胃溃疡愈合的刺激作用的基础。