Literature DB >> 9233696

Long-term function of fish islet xenografts in mice by alginate encapsulation.

H Yang1, W O'Hali, H Kearns, J R Wright.   

Abstract

BACKGROUND: Large, anatomically discrete pancreatic islets, Brockmann bodies (BBs), exist in certain teleost fish. When transplanted under the renal capsules of streptozotocin-diabetic athymic nude mice, BB grafts produce uniform normoglycemia for 50 days and mammalian-like glucose tolerance profiles; however, these very discordant islets reject in 7-8 days when transplanted into euthymic BALB/c mice.
METHODS: In the present study, BBs were mass harvested, minced into <1-mm tissue fragments, and encapsulated in alginate-based macrospheres (5 mm diameter) or noodles (0.5x3 cm). Nonencapsulated and encapsulated BB fragments were transplanted intraperitoneally into streptozotocin-diabetic (nonfasting blood glucose >400 mg/dl) nu/nu and BALB/c mice. Glucose levels were monitored at least 3 times a week.
RESULTS: Encapsulated BB grafts uniformly survived >50 days (10/10) or >100 days (3/3) in nu/nu recipients. The mean graft survival time was 27+/-13 days in BALB/c recipients (n=7). Daily intraperitoneal administration of 2.5 mg/kg 15-deoxyspergualin, in combination with encapsulation, resulted in uniform long-term BB graft function in BALB/c recipients (n=5). Similarly, long-term function was achieved in four of six BALB/c recipients with daily intraperitoneal administration of 10 mg/kg cyclosporine (two grafts failed after 39 and 45 days). Nonencapsulated BB grafts transplanted intraperitoneally into BALB/c or nu/nu recipients functioned for <7 days; immunosuppression alone did not permit graft survival in BALB/c recipients. In all cases of graft survival of >50 days, grafts were surgically removed from the peritoneal cavity, and blood sugar levels returned to a diabetic state within a few days. Historical sections of grafts, stained with hematoxylin and eosin and immunoperoxidase for insulin, showed viable, well-granulated BB tissue.
CONCLUSIONS: This study demonstrates that tilapia BBs are suitable for encapsulation and that encapsulated BBs can be made to function long term in diabetic mice.

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Year:  1997        PMID: 9233696     DOI: 10.1097/00007890-199707150-00006

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  5 in total

Review 1.  Islet and stem cell encapsulation for clinical transplantation.

Authors:  Rahul Krishnan; Michael Alexander; Lourdes Robles; Clarence E Foster; Jonathan R T Lakey
Journal:  Rev Diabet Stud       Date:  2014-05-10

Review 2.  Toward beta cell replacement for diabetes.

Authors:  Bjarki Johannesson; Lina Sui; Donald O Freytes; Remi J Creusot; Dieter Egli
Journal:  EMBO J       Date:  2015-03-01       Impact factor: 11.598

3.  Production of transgenic tilapia with Brockmann bodies secreting [desThrB30] human insulin.

Authors:  Bill Pohajdak; Marc Mansour; Olga Hrytsenko; J Michael Conlon; L Clayton Dymond; James R Wright
Journal:  Transgenic Res       Date:  2004-08       Impact factor: 2.788

4.  Ancestral genomic duplication of the insulin gene in tilapia: An analysis of possible implications for clinical islet xenotransplantation using donor islets from transgenic tilapia expressing a humanized insulin gene.

Authors:  Olga Hrytsenko; Bill Pohajdak; James R Wright
Journal:  Islets       Date:  2016-07-03       Impact factor: 2.694

Review 5.  A review of piscine islet xenotransplantation using wild-type tilapia donors and the production of transgenic tilapia expressing a "humanized" tilapia insulin.

Authors:  James R Wright; Hua Yang; Olga Hyrtsenko; Bao-You Xu; Weiming Yu; Bill Pohajdak
Journal:  Xenotransplantation       Date:  2014-07-05       Impact factor: 3.907

  5 in total

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