Summary
Whether cultured human trabecular meshwork cells express transforming growth factor-β2 (TGF-β2) messenger RNA (mRNA) and protein was investigated. Total RNA of 106 cultured human trabecular meshwork cells was extracted with TRIZOL reagent, reverse transcriptase-polymerase chain reaction (RT-PCR) were used for detection of TGF-β2 messenger RNA, and the PCR product was verified by sequencing. Immunohistochemical staining was used to detect TGF-β2 protein. The results showed that a single RT-PCR amplified product was obtained, and the sequence was homologous to the known sequence. TGF-β2 immunostaining was positive. It was concluded that trabecular meshwork cells could produce TGF-β2 and contribute to the presence of TGF-β2 in trabecular meshwork microenvironment as well as aqueous humor. Trabecular meshwork cells were affected by TGF-β2 not only through paracrine, but also autocrine action. Whether abnormal changes in TGF-β2 production contribute to the pathogenesis of primary open-angle glaucoma is worth further investigation.
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CAO Yang, male, born in 1972, M. D., Ph. D., Doctor in Charge
This project was supported by the National Natural Science Foundation of China (Serial No. 38970758).
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Yang, C., Houren, W., Banghong, D. et al. Transforming growth factor-β2 gene cloning and protein expression in human trabecular meshwork cells. Current Medical Science 23, 85–87 (2003). https://doi.org/10.1007/BF02829473
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DOI: https://doi.org/10.1007/BF02829473