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Bacterial lipopolysaccharides in sterile corneal organ-culture media.

作者信息

Sobottka Ventura A C, Böhnke M

机构信息

Augen- und Poliklinik des Inselspitals, Universität Bern, Switzerland.

出版信息

Cornea. 1999 Jan;18(1):92-7.

PMID:9894944
Abstract

PURPOSE

Lipopolysaccharides (LPS) are known to stimulate various inflammatory reactions by interaction with cytokines and macrophages. As contamination of sterile organ culture media with nonviable bacterial substances may influence donor tissue prognosis, we investigated a series of culture media drawn from organ culture for the presence of LPS.

METHODS

One hundred eighty-two samples of sterile organ-culture media were tested for LPS using the Limulus-amoebocyte-lysate assay (LALA). We then investigated the time course of LPS levels during organ culture, the influence of medium changes, the graft deswelling procedure and transportation as well as repeated freezing on the detection of lipopolysaccharides with the LALA.

RESULTS

LPS above background threshold was found in 21.4% of the organ-culture media. The time course of LPS during organ culture and through the deswelling procedure was quite stable. Medium changes may wash out LPS, thus the highest LPS values were normally seen in the examination medium, which has the first contact with the corneal tissue. Repeated freezing did not influence the detectability of LPS with the LALA.

CONCLUSION

LPS detected in sterile corneal organ cultures is probably derived from nonreplicating bacterial postmortem donor tissue contamination. It is a rather heat and cold stable product that may be washed out from the donor tissue by medium changes. As LPS may directly influence graft viability or trigger inflammatory host responses, further investigations of the clinical course of these grafts are required.

摘要

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