Wordinger R J, Lambert W, Agarwal R, Talati M, Clark A F
Department of Anatomy and Cell Biology and The North Texas Eye Research Institute, University of North Texas Health Science Center at Fort Worth. Glaucoma Research, Alcon Research, Ltd., Fort Worth, Texas, USA.
Invest Ophthalmol Vis Sci. 2000 Nov;41(12):3833-41.
The purpose of this study was to compare the mRNA expression of neurotrophins (NTs) and NT receptors (Trk) in cultured human trabecular meshwork (HTM) cells and ex vivo HTM tissues, to immunolocalize both NT and Trk receptors in cultured HTM cells, and to demonstrate secretion of NTs by HTM cells.
Reverse transcription-polymerase chain reaction (RT-PCR) was used to detect the expression of NT and Trk receptor mRNAs in early-passaged, cultured HTM cells from donors of several ages. RT-PCR was used on ex vivo HTM tissues from donors to compare and contrast mRNA expression with cell culture results. In addition, immunohistochemistry was used to localize the translated NT and low- (p75) and high- (Trk) affinity NT receptor proteins within cultured HTM cells and trabecular meshwork tissues. Last, enzyme-linked immunoassay (ELISA) was used to demonstrate secretion of NTs by HTM cells.
Amplification products of the expected size for NTs were detected in both cultured HTM cells and ex vivo HTM tissues. Specifically identified were amplification products for the following NTs: NGF, BDNF, NT-3, and NT-4. Amplification products for the full-length Trk A and Trk C high-affinity receptor were observed, as well as truncated isoforms for Trk B and Trk C. No amplification products were produced for the full-length Trk B receptor nor for the low-affinity p75 receptor. Immunohistochemistry indicated that proteins for the various NTs and full-length and truncated Trk receptors were translated by cultured HTM cells and tissues. Immunoassays (ELISA) detected BDNF, NT-4, NGF, and NT-3 in the culture media from HTM cells.
The results demonstrate, for the first time, mRNA expression for NT and Trk receptors by both cultured HTM cells and ex vivo HTM tissues. NTs were immunolocalized in HTM tissues and cultured HTM cells are capable of secreting NTs. Specific NTs acting through high-affinity Trk receptors within the HTM may be involved in maintaining the normal function of this complex tissue.
本研究旨在比较培养的人小梁网(HTM)细胞和离体HTM组织中神经营养因子(NTs)及其受体(Trk)的mRNA表达,对培养的HTM细胞中的NTs和Trk受体进行免疫定位,并证明HTM细胞分泌NTs。
采用逆转录-聚合酶链反应(RT-PCR)检测来自不同年龄供体的早期传代培养HTM细胞中NTs和Trk受体mRNA的表达。对来自供体的离体HTM组织进行RT-PCR,以比较和对比mRNA表达与细胞培养结果。此外,采用免疫组织化学方法在培养的HTM细胞和小梁网组织中定位翻译后的NTs以及低亲和力(p75)和高亲和力(Trk)NTs受体蛋白。最后,采用酶联免疫吸附测定(ELISA)证明HTM细胞分泌NTs。
在培养的HTM细胞和离体HTM组织中均检测到预期大小的NTs扩增产物。具体鉴定出以下NTs的扩增产物:神经生长因子(NGF)、脑源性神经营养因子(BDNF)、神经营养因子-3(NT-3)和神经营养因子-4(NT-4)。观察到全长Trk A和Trk C高亲和力受体的扩增产物,以及Trk B和Trk C的截短异构体。未产生全长Trk B受体和低亲和力p75受体的扩增产物。免疫组织化学表明,培养的HTM细胞和组织翻译出了各种NTs以及全长和截短的Trk受体蛋白。免疫测定(ELISA)在HTM细胞的培养基中检测到BDNF、NT-4、NGF和NT-3。
结果首次证明,培养的HTM细胞和离体HTM组织均表达NTs和Trk受体的mRNA。NTs在HTM组织中进行了免疫定位,培养的HTM细胞能够分泌NTs。通过HTM内高亲和力Trk受体起作用的特定NTs可能参与维持这一复杂组织的正常功能。