Nguyen D H, Beuerman R W, Thompson H W, DiLoreto D A
Department of Ophthalmology, LSU Eye Center, Louisiana State University Medical Center School of Medicine, New Orleans 70112, USA.
Cornea. 1997 Mar;16(2):192-9.
This study examined the expression of important growth factor and receptor messenger RNA (mRNA) in human lacrimal gland.
Lacrimal gland tissue was obtained from six women, aged 31-85 years, who were undergoing surgery. The specimens were frozen immediately in liquid nitrogen. Total cellular RNA was collected by cesium chloride centrifugation, and the integrity of the RNA was analyzed by gel electrophoresis and spectrophotometry. For the reverse-transcription polymerase chain reaction (RT-PCR) procedure, 1 microgram of total cellular RNA was used for the first strand synthesis and amplified in separate reactions for 34 cycles by using primers specific for transforming growth factor-beta 1, -beta 2, and -beta 3 (TGF beta 1, TGF beta 2, TGF beta 3), TGF beta 3 receptor (TGF beta 3R), basic fibroblast growth factor (bFGF), fibroblast growth factor receptor-1 (FGF-R1), nerve growth factor (beta-NGF), low-affinity NGF receptor (p75NGF-R), and platelet-derived growth factor-AA (PDGF-AA; two of the six cases) and -BB (PDGF-BB; three of the six cases). Product identity was confirmed by restriction endonuclease digestion, by the "hot blot" technique, by DNA sequencing, or by a combination of these.
All the lacrimal gland specimens were positive for all growth factors, neurotrophic factors, and receptors except for two specimens that were negative for bFGF. The patients from whom the bFGF-negative specimens were obtained were 68 and 74 years old, and both were identified as having dry eyes-one severe and the other moderate, respectively. These specimens were also analyzed for PDGF-AA and PDGF-BB mRNA, and both were positive.
This study demonstrates that RT-PCR is a rapid and sensitive method for analyzing rare mRNA transcripts in small amounts of tissue. The results suggest that these growth and neurotrophic factors may have autocrine and paracrine roles in modulating the lacrimal gland, and their absence may play a role in pathologic states such as fibrosis and dry eyes.
本研究检测了重要生长因子及其受体信使核糖核酸(mRNA)在人泪腺中的表达。
从6名年龄在31至85岁接受手术的女性身上获取泪腺组织。标本立即在液氮中冷冻。通过氯化铯离心收集总细胞RNA,并通过凝胶电泳和分光光度法分析RNA的完整性。对于逆转录聚合酶链反应(RT-PCR)程序,使用1微克总细胞RNA进行第一链合成,并使用针对转化生长因子-β1、-β2和-β3(TGFβ1、TGFβ2、TGFβ3)、TGFβ3受体(TGFβ3R)、碱性成纤维细胞生长因子(bFGF)、成纤维细胞生长因子受体-1(FGF-R1)、神经生长因子(β-NGF)、低亲和力NGF受体(p75NGF-R)以及血小板衍生生长因子-AA(PDGF-AA;6例中的2例)和-BB(PDGF-BB;6例中的3例)的特异性引物在单独反应中扩增34个循环。通过限制性内切酶消化、“热印迹”技术、DNA测序或这些方法的组合来确认产物的同一性。
除2份标本bFGF呈阴性外,所有泪腺标本的所有生长因子、神经营养因子和受体均呈阳性。获得bFGF阴性标本的患者年龄分别为68岁和74岁,两人分别被诊断为患有干眼症,一人为重度,另一人为中度。还对这些标本进行了PDGF-AA和PDGF-BB mRNA分析,两者均为阳性。
本研究表明,RT-PCR是一种用于分析少量组织中稀有mRNA转录本的快速且灵敏的方法。结果提示,这些生长因子和神经营养因子可能在调节泪腺方面具有自分泌和旁分泌作用,而它们的缺失可能在诸如纤维化和干眼症等病理状态中起作用。