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. 2001 Dec;85(12):1416–1420. doi: 10.1136/bjo.85.12.1416

Effect of three different media on serum free culture of donor corneas and isolated human corneal endothelial cells

J Bednarz 1, V Doubilei 1, P Wollnik 1, K Engelmann 1
PMCID: PMC1723804  PMID: 11734511

Abstract

BACKGROUND—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.
METHODS—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.
RESULTS—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.
CONCLUSION—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.



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Figure 1  .

Figure 1  

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Proliferation of isolated human corneal endothelial cells during culture in medium MEM (A), F99 (B), and Endothelial-SFM (C). Cells were seeded on six well plates (2000 cells/well) and cultured using the indicated medium without serum supplementation or in the presence of 0.05%, 0.1%, 0.5%, 1%, or 5% FCS, respectively. The number of cells was determined after 4, 5, 6, 7, 8, and 11 days of culture. Indicated cell amounts are means (SD) of six independent experiments.

Figure 2  .

Figure 2  

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Endothelial cell loss of donor corneas during organ culture in medium MEM, F99, and Endothelial-SFM (SFM) with or without supplementation of 2% FCS. Cell densities were determined at the beginning of organ culture and then every week. Indicated are the means (SD) for the decrease in endothelial cell density determined from seven corneas.

Figure 3  .

Figure 3  

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Analysis of damaged endothelium after 3 weeks of organ culture by means of trypan blue staining. Indicated are the means (SD) of the percentage of blue stained endothelial cells from seven corneas cultivated in the indicated medium with or without 2% FCS supplementation. Statistical analysis revealed the following results:
p Value Significance
MEM with FCS versus SFM with FCS 0.036 Yes
MEM without FCS versus SFM without FCS 0.003 Yes
MEM with FCS versus F99 with FCS 0.260 No
MEM without FCS versus F99 without FCS 0.012 Yes
F99 with FCS versus SFM with FCS 0.132 No
F99 without FCS versus SFM without FCS 0.018 Yes
SFM with FCS versus SFM without FCS 0.943 No
MEM with FCS versus MEM without FCS 0.100 No
F99 with FCS versus F99 without FCS 1.000 No
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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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