Leicester Research Archive

Leicester Research Archive >
College of Medicine, Biological Sciences and Psychology >
Infection, Immunity and Inflammation, Department of >
Published Articles, Dept. of Infection, Immunity and Inflammation >

Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/1317

Title: Characterisation of an important enzymatic component in collagenase that is essential for the effective digestion of the human and porcine pancreas
Authors: Chen, R.L.
James, Roger F.L.
Issue Date: 2001
Publisher: Cognizant Communication Corporation
Citation: Cell Transplantation, 2001, 10 (8), pp.709-716
Abstract: Recent clinical results from Edmonton have demonstrated the feasibility of achieving normoglycemia in type I diabetic patients by islet transplantation. One of the key issues in obtaining this success was transplanting sufficient numbers of islets by sequential transplants. Although the development of semipurified endotoxin-free Clostridium histolyticum-derived collagenase (Liberase) has improved islet yields from the human pancreas, batch-to-batch variation and loss of activity with time still hampers progress in obtaining consistent islet preparations. In order to define key components of crude collagenase, a panel of monoclonal antibodies (McAbs) was raised against crude collagenase. Monoclonal antibodies were generated by fusions between splenocytes of BALB/c mice immunized with Boheringer P collagenase and the myeloma cell line NS-0. These monoclonal antibodies were used as probes to study molecular differences between effective and ineffective collagenase batches using Western blotting. Two monoclonal antibodies (LDS71 and LDS81) were raised and characterized as recognizing separate epitopes on a 125-kDa component. Western blotting indicated that the 125-kDa band was rapidly broken down by storage or by dialysis in the presence of dithiothreitol. However, this breakdown could be prevented by the addition of leupeptin (a protease inhibitor) to the dialysis buffer. On testing fractions at 5-min intervals from the “Ricordi” digestion circuit during porcine and human pancreas digestion, the 125-kDa component was rapidly broken down in relatively ineffective collagenase batches but in effective batches was present throughout the digestion process. The correlation between the presence of the 125-kDa band and effectiveness of pancreas digestion suggests that this may be a key component in the formulation of C. histolyticum collagenase.
ISSN: 0963-6897
eISSN: 1555-3892
Links: http://hdl.handle.net/2381/1317
http://www.ingentaconnect.com/content/cog(...)
Version: Publisher version
Status: Peer reviewed
Type: Article
Rights: Copyight 2001 Cognizant Comm. Corp. Deposited with reference to the publisher's archiving policy available on the SHERPA/RoMEO website.
Appears in Collections:Published Articles, Dept. of Infection, Immunity and Inflammation

Files in This Item:

File Description SizeFormat
8650256_amended.pdf1.96 MBAdobe PDFView/Open
View Statistics

Items in LRA are protected by copyright, with all rights reserved, unless otherwise indicated.

 

MAINTAINER