Bednarz J, Doubilei V, Wollnik P C, Engelmann K
Universitäts-Augenklinik Eppendorf, Martinistrasse 52, D-20246 Hamburg, Germany.
Br J Ophthalmol. 2001 Dec;85(12):1416-20. doi: 10.1136/bjo.85.12.1416.
Removal of bovine serum from organ culture medium is necessary because of the variability in serum composition and the potential risk of infection. Two specific endothelial cell media (F99 and Endothelial-SFM) were compared with the routinely used medium MEM for their use in serum free cultivation of human corneal endothelial cells (HCEC) and donor corneas.
HCEC were incubated in three test media with or without increasing serum content and a growth assay was performed. Seven pairs of donor corneas were cultured in each of three media for 3 weeks, one cornea with serum supplementation and one without. Endothelial cell density was determined once each week. Trypan blue staining of the endothelium and vital staining of keratocytes was performed after 3 weeks.
All three media promoted proliferation of cultured HCEC when supplemented with serum. Endothelial cell density of donor corneas was comparable after 3 weeks of cultivation in the different media. Only corneas cultured in medium MEM without serum exhibited a higher endothelial cell loss. Trypan blue staining of the endothelium after cultivation revealed the lowest number of damaged cells on corneas cultured in the medium Endothelial-SFM. The highest densities of keratocytes were found in corneas cultured in Endothelial-SFM and the lowest densities occurred after culture in MEM.
After incubation in Endothelial-SFM even under serum free conditions corneas were found to be of higher quality with respect to endothelial cell survival, cell membrane integrity, and keratocyte density. This medium may replace MEM, which is routinely used in European eye banks but requires supplementation with serum.
由于血清成分的变异性和潜在的感染风险,从器官培养基中去除牛血清是必要的。将两种特定的内皮细胞培养基(F99和内皮细胞无血清培养基)与常规使用的培养基MEM进行比较,以用于人角膜内皮细胞(HCEC)和供体角膜的无血清培养。
将HCEC在三种测试培养基中培养,添加或不添加增加的血清含量,并进行生长测定。七对供体角膜在三种培养基中的每一种中培养3周,一对角膜添加血清,另一对不添加。每周测定一次内皮细胞密度。3周后对内皮进行台盼蓝染色,对角细胞进行活体染色。
当添加血清时,所有三种培养基均促进培养的HCEC增殖。在不同培养基中培养3周后,供体角膜的内皮细胞密度相当。仅在无血清的MEM培养基中培养的角膜内皮细胞损失较高。培养后内皮的台盼蓝染色显示,在内皮细胞无血清培养基中培养的角膜上受损细胞数量最少。在内皮细胞无血清培养基中培养的角膜中发现角细胞密度最高,在MEM培养基中培养后角细胞密度最低。
在内皮细胞无血清培养基中孵育后,即使在无血清条件下,角膜在内皮细胞存活、细胞膜完整性和角细胞密度方面的质量也更高。这种培养基可能会取代欧洲眼库常规使用但需要添加血清的MEM培养基。