Production and characterization of fetal sheep pancreatic islet-like cell clusters

1996 ◽  
Vol 5 (4) ◽  
pp. 491-498 ◽  
Author(s):  
B Tuch
1996 ◽  
Vol 5 (4) ◽  
pp. 491-498 ◽  
Author(s):  
Bernard E. Tuch ◽  
Jocelyn C. Madrid ◽  
Ellie Summers ◽  
Murray S.R. Smith

Explants of fetal sheep pancreas transplanted into diabetic athymic mice survive for many months but there is only partial differentiation of the endocrine cells. As an alternative form of graft we examined the possibility of creating islet-like cell clusters (ICCs) by collagenase digestion of the fetal sheep pancreas, as has been described for human and porcine fetal pancreas. Such ICCs did form at the rate of 6-23 per 10 mg pancreas; their size varied between 65 and 474 μm (median 232 μm) and their insulin content was 1.6 ± 0.2 mU per 20 ICCs. Laser scanning confocal analysis showed that 4.6 ± 0.7% of the cells contained insulin. Insulin was secreted from ICCs maintained in culture at the daily rate of 2.5 mU per 30 ICCs. Arginine but not glucose or theophylline enhanced acute insulin secretion in vitro. Transplantation of up to 1000 ICCs into athymic and scid mice resulted in sparse growth of the epithelial-like cells in the graft and only partial differentiation of the endocrine cells. Hyperglycaemia in diabetic recipients was not normalized. Thus, while functioning ICCs can be created from fetal sheep pancreas, they do not appear to be appropriate for transplantation to reverse diabetes in mice.


Peptides ◽  
1985 ◽  
Vol 6 (3) ◽  
pp. 483-489 ◽  
Author(s):  
C.E. Dunlap ◽  
D.K. Sundberg ◽  
J.C. Rose

Nature ◽  
1982 ◽  
Vol 300 (5889) ◽  
pp. 276-278 ◽  
Author(s):  
Jean Rivier ◽  
Joachim Spiess ◽  
Michael Thorner ◽  
Wylie Vale

1995 ◽  
Vol 34 (3) ◽  
pp. 439-448 ◽  
Author(s):  
Yoshiaki NORIMATSU ◽  
Hiromi KODA ◽  
Shuji HAMAZAKI ◽  
Yuri OZEKI ◽  
Kyoumi NAKAKUNI ◽  
...  

2015 ◽  
Vol 43 (5) ◽  
pp. 743-746 ◽  
Author(s):  
Akiko Anagawa-Nakamura ◽  
Kochi Kakimoto ◽  
Katsuhiro Miyajima ◽  
Yuzo Yasui ◽  
Yusuke Kemmochi ◽  
...  

1999 ◽  
Vol 266 (1) ◽  
pp. 33-36 ◽  
Author(s):  
Ilias Nitsos ◽  
David W Walker
Keyword(s):  

2020 ◽  
Vol 150 (8) ◽  
pp. 2061-2069
Author(s):  
Brit H Boehmer ◽  
Laura D Brown ◽  
Stephanie R Wesolowski ◽  
William W Hay ◽  
Paul J Rozance

ABSTRACT Background Infusion of a complete amino acid mixture into normal late-gestation fetal sheep potentiates glucose-stimulated insulin secretion (GSIS). Leucine acutely stimulates insulin secretion in late-gestation fetal sheep and isolated fetal sheep islets in vitro. Objectives We hypothesized that a 9-d leucine infusion would potentiate GSIS in fetal sheep. Methods Columbia-Rambouillet fetal sheep at 126 days of gestation received a 9-d leucine infusion to achieve a 50%–100% increase in leucine concentrations or a control infusion. At the end of the infusion we measured GSIS, pancreatic morphology, and expression of pancreatic mRNAs. Pancreatic islet endothelial cells (ECs) were isolated from fetal sheep and incubated with supplemental leucine or vascular endothelial growth factor A (VEGFA) followed by collection of mRNA. Data measured at multiple time points were compared with a repeated-measures 2-factor ANOVA. Data measured at 1 time point were compared using Student's t test or the Mann–Whitney test. Results Glucose-stimulated insulin concentrations were 80% higher in leucine-infused (LEU) fetuses than in controls (P < 0.05). In the pancreas, LEU fetuses had a higher proportion of islets >5000 μm2 than controls (75% more islets >5000 μm2; P < 0.05) and a larger proportion of the pancreas that stained for β cells (12% greater; P < 0.05). Pancreatic and pancreatic islet vascularity were both 25% greater in LEU fetuses (P < 0.05). Pancreatic VEGFA and hepatocyte growth factor (HGF) mRNA expressions were 38% and 200% greater in LEU fetuses than in controls (P < 0.05), respectively. In isolated islet ECs, HGF mRNA was 20% and 50% higher after incubation in supplemental leucine (P < 0.05) or VEGFA (P < 0.01), respectively. Conclusions A 9-d leucine infusion potentiates fetal GSIS, demonstrating that glucose and leucine act synergistically to stimulate insulin secretion in fetal sheep. A greater proportion of the pancreas being comprised of β cells and higher pancreatic vascularity contributed to the higher GSIS.


1995 ◽  
Vol 2 (1) ◽  
pp. 26-31 ◽  
Author(s):  
A. Bjöersdorff ◽  
O. Korsgren ◽  
R. Feinstein ◽  
A. Andersson ◽  
J. Tollemar ◽  
...  
Keyword(s):  

2017 ◽  
Vol 49 (12) ◽  
pp. 957-962 ◽  
Author(s):  
Celso Gomez-Sanchez ◽  
Maniselvan Kuppusamy ◽  
Martin Reincke ◽  
Tracy Williams

AbstractPrimary aldosteronism is the most common type of secondary hypertension affecting 6–10% of patients with primary hypertension. PA is mainly caused by unilateral hyperaldosteronism due to an aldosterone-producing adenoma, unilateral hyperplasia with or without micronodules or bilateral zona glomerulosa hyperplasias with or without macro or micronodules. The development of antibodies against the terminal enzyme of aldosterone biosynthesis (CYP11B2) has permitted the further characterization of normal adrenals and resected adrenals from patients with primary aldosteronism. Normal adrenals exhibit two different patterns of cellular expression of CYP11B2: young individuals display a relatively uniform expression of the enzyme throughout the zona glomerulosa while the adrenals of older individuals have dispersed CYP11B2-expressing cells but have more groups of cells called aldosterone-producing cell clusters (APCC). APAs exhibit different patterns of CYP11B2 staining that vary from uniform to homogeneous. There are also a proportion of cells within the APA that co-express different enzymes that are not normally co-expressed in normal individuals. Approximately 30% of patients with unilateral hyperaldosteronism do not have an APA, but either have an increased number of CYP11B2 expressing micronodules or hyperplasia of the zona glomerulosa. In summary, the studies reported in this review are shedding new light on the pathophysiology of primary aldosteronism. The wide variation in histopathological features of the adenomas and concurrent presence of APCCs raises the possibility that most cases of unilateral production of aldosterone actually might represent bilateral asymmetric hyperplasia with nodules frequently due to the development of somatic aldosterone-driving mutations.


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