Spurr-Michaud Sandra, Argüeso Pablo, Gipson Ilene
Schepens Eye Research Institute, 20 Staniford Street, Boston, MA 02114, USA.
Exp Eye Res. 2007 May;84(5):939-50. doi: 10.1016/j.exer.2007.01.018. Epub 2007 Feb 7.
Mucin genes, both secreted (MUC2, MUC5AC, MUC5B, MUC7) and membrane associated (MUC1, MUC4, MUC16), have been reported to be expressed by ocular surface epithelia. The purpose of this study was to comprehensively assay the mucin content of human tear fluid using multiple antibodies for each mucin and to develop a sensitive, semi-quantitative method for the assay of mucins in tears. Tear washes were obtained by instillation of saline onto the ocular surface, followed by collection from the inferior fornix. Tear proteins were separated in 1% agarose gels, transferred to nitrocellulose membrane by vacuum blotting and probed with multiple antibodies recognizing MUC1, MUC2, MUC4, MUC5AC, MUC5B, MUC7 and MUC16. Binding was detected using chemiluminescence, and quantity was determined by densitometry. Serial dilutions of pooled tears from normal individuals were assayed to determine the linear range of detectability. MUC1, MUC4, MUC16, MUC5AC and low levels of MUC2 were consistently detected in human tear fluid, while MUC5B and MUC7 were not. Use of several antibodies recognizing different epitopes on the same mucin confirmed these findings. The antibodies to mucins bound to serial dilutions of tears in a linear fashion (r2 > 0.9), indicating the feasibility of semi-quantitation. MUC5AC in tear fluid had an increased electrophoretic mobility compared to MUC5AC isolated from conjunctival tissue. This study provides clear evidence that the mucin component of tears is a mixture of secreted and shed membrane-associated mucins, and for the first time demonstrates MUC16 in tear fluid. Immunoblots of tears using agarose gel electrophoresis and chemiluminescence detection provide a semi-quantitative assay for mucin protein that will be useful for comparisons with tears from diseased eyes or after pharmacological intervention.
据报道,分泌型(MUC2、MUC5AC、MUC5B、MUC7)和膜相关型(MUC1、MUC4、MUC16)黏蛋白基因均在眼表上皮中表达。本研究的目的是使用针对每种黏蛋白的多种抗体全面检测人泪液中的黏蛋白含量,并开发一种灵敏的半定量方法来检测泪液中的黏蛋白。通过将盐水滴入眼表,然后从下穹窿收集来获取泪液冲洗液。泪液蛋白在1%琼脂糖凝胶中分离,通过真空印迹转移到硝酸纤维素膜上,并用识别MUC1、MUC2、MUC4、MUC5AC、MUC5B、MUC7和MUC16的多种抗体进行检测。使用化学发光检测结合情况,并通过密度测定法定量。对正常个体混合泪液进行系列稀释检测,以确定可检测的线性范围。在人泪液中始终检测到MUC1、MUC4、MUC16、MUC5AC和低水平的MUC2,而未检测到MUC5B和MUC7。使用识别同一黏蛋白上不同表位的多种抗体证实了这些发现。黏蛋白抗体与泪液系列稀释液呈线性结合(r2>0.9),表明半定量的可行性。与从结膜组织分离的MUC5AC相比,泪液中的MUC5AC具有增加的电泳迁移率。本研究提供了明确证据,表明泪液的黏蛋白成分是分泌型和脱落的膜相关黏蛋白的混合物,并且首次在泪液中证实了MUC16。使用琼脂糖凝胶电泳和化学发光检测的泪液免疫印迹为黏蛋白提供了一种半定量检测方法,这将有助于与患病眼或药物干预后的泪液进行比较。