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Objective: To investigate the role of connective tissue growth factor (CTGF) after trabeculectomy associated with wound healing and to identify the role of CTGF in this process., Methods: It was a experimental study. Forty-nine rabbits were used and divided into 5 groups: normal eyes without trabeculectomy group (group A), ocular hypertension (OHT) model without trabeculectomy group (group B), OHT model with trabeculectomy group (group C), normal eyes with trabeculectomy group (group D) and normal eyes with sham operation group (group E). Group A and B were as control. CTGF mRNA was detected by RT-PCR using blebs and tissues harvested at day 2, 5, 7, and 14. Three replicates of three blebs per time point in the right eyes were collected. The expression of CTGF protein was detected by immunohistochemistry and inflammatory histopathology was inspected by HE staining using the whole eyeball harvested in the left eyes., Results: Compared to group A and B, the expression of CTGF was significantly increased at day 5 after surgery (F = 19.54, P < 0.05) in group C, D, and E. The expression of CTGF mRNA in group C is significantly higher than that in group D at day 2 and 5 (t = 2.300, 5.140, P < 0.05), while group D is significantly higher than that in group E at day 2, 5, 7, and 14 (t = -2.927, -6.424, -4.176, -4.997, P < 0.05). The expression of CTGF protein in group C is significantly higher than that in group D (t = -7.147, -10.955, -9.900, -6.385, P < 0.05), and group D is higher than that in group E (F = 68.33, P < 0.05) at day 2, 5, 7, and 14, respectively. Inflammatory reaction reached peak at day 5 after surgery in group C, D, and E showing an infiltration of neutrophil, monocytes, macrophages, and the proliferation of fibroblast., Conclusions: Overexpression of CTGF in the blebs after trabeculectomy demonstrates that CTGF may play an important role in the process of wound healing. Furthermore, ocular hypertension may be involved in the upregulation of CTGF expression.

Objective: To identify the mutation gene of two Chinese families with primary open angle glaucoma., Methods: It was a case control study. Clinical observation and pedigree analysis were undertaken in two families with primary open angle glaucoma. Venous blood were drawn from 6 affected and 6 unaffected subjects in family L, and from 4 affected and 4 unaffected subjects in family C. Genomic DNA was extracted. Linkage to OPTN gene locus was determined. Mutation of this gene was screened by PCR of OPTN gene exons and direct sequencing., Results: A missense mutation A1274G in exon 10 of OPTN gene was identified in affected members of family L. The corresponding amino acid change was Lys322Glu. This mutation was not found in unaffected family members of family L, all members of family C and 87 unrelated normal controls., Conclusion: A novel mutation of OPTN gene with Lys322Glu change is responsible for the occurrence of primary open angle glaucoma in a Chinese family.

Objective: To investigate the prevalence of primary angle-closure glaucoma (PACG) and its causes in a rural area in Changchun, China., Methods: From the rural area of Qijiaxiang, Shuangyang district of Changchun, 1139 individuals aged 40 years and above were randomly selected for the study from September 2004 to February 2005 using Zhao Jialiang's standard. All subjects in this study underwent a preliminary screening examination including visual acuity, the peripheral depth of anterior chamber, slit lamp, tonometry and fundus. The suspects of PACG were asked to repeat the following examinations: tonometry, gonioscopy, fundus, and visual field assessment., Results: 1139 of 1528 subjects were invited to participate in the study (response rate 74.5%). In those age 40 years and above, the prevalence of PACG was 1.5% in men, 3.5% in women, and 2.5% in general population, respectively. The prevalence was increased with age. The anterior chamber was significantly (P<0.01) narrower in the female group than in the male group when the peripheral depth of anterior chamber was compared. The prevalence of PACG was significantly (P<0.02) higher in subjects with positive family history than with negative family history., Conclusions: In the rural area in Shuangyang district of Changchun, the prevalence of PACG is higher than other regions surveyed in China. Sex, age, family history and the peripheral depth of anterior chamber are significant risk factors in PACG.

Objective: To analysis the association of apolipoprotein E (APOE) genotype with primary open-angle glaucoma (POAG) and primary angle-closure glaucoma (PACG) in northeast of China., Method: The polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) technique were used to detect the distribution of genotype and gene frequency of APOE alleles in 36 patients with POAG, 69 with PACG and 57 healthy subjects as control., Results: The frequency of APOE epsilon 3/epsilon 4 genotype in POAG group (41.7%)and epsilon 2/epsilon 4 in PACG group (43.5%) was significantly (P < 0.05) higher than that in control group (14.0% and 21.1%, respectively). The frequency of APOE epsilon 4 allele in both of POAG (37.5%) and PACG group (39.2%) was significantly (P < 0.05) higher than that in control group (17.5%), whereas the frequency of APOE epsilon 2 allele in POAG group (8.3%) was significantly (P < 0.05) lower than that in control group (15.8%)., Conclusion: APOE epsilon 4 allele may be a latent risk factor in the development of primary glaucoma, but APOE epsilon 2 allele may play a protective role in POAG and warrant further investigation.

Objective: To study the cultivation and differentiation of neural stem cells (NSC) in vitro and observe the effects of retinal cell-conditioned medium on the differentiation of NSC., Method: Cells from subependymal zone of postnatal 0 - 3 days SD rat were isolated and cultured in vitro. Retinal cells of SD rat were cultured simultaneously. The supernatants (conditioned medium, SDR-CM) of cultured retinal cells were collected and used for the cultivation of the NSC from subependymal zone. Immunofluorescence method and anti-Thy1.1 antibodies were used to identify the cells derived from the NSC., Results: Cultured NSC grew well in the serum-free culture medium. Cultured subependymal cells in the SDR-CM could be differentiated to the retinal cells. Some cells were stained positively with anti-Thy1.1 antibodies., Conclusion: These results showed that cultured NSC could survive well in vitro. SDR-CM can induce the NSC to differentiate to the retinal cells. The present study was designed to simulate the microenvironment of the eyes and to induce the differentiation of the NSC. Our in vitro model system may provide theoretical basis for the intraocular transplantation of retinal neurons.