Secondary Negative Effects of Isolation Enzyme (s) On Human Islets. A.N.Balamurugan

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Transcription:

Secondary Negative Effects of Isolation Enzyme (s) On Human Islets A.N.Balamurugan

Human Islets Functional Mass Preservation

18-25 min 10 min 8-12 min 10-15 min 45-60 min pancreas in chamber 37º Sub-Optimal Pancreases free islets warm collection cold end recirculation dilution cold collection end digestion Beginning of Cold End of Digestion

ISLET INCUBATION PROTOCOL Organ Manipulation - Ricordi s isolation method Start Warm collection T = 8-12 Minutes Sampling Wash Cells and Maintain at 4C Appearance of Free Islets Incubate at 37C With No Washing SAMPLES Islet Count DNA Measurement Insulin Content Immunocytochemistry Start Cold collection T = 25-30 Minutes 4C Samples 37C Samples

Insulin Immunostaining Standard Collection 80% 00% 60% 37 Cº 40% 4º 20% 0% <50 50-100 100-150 150-200 >200 Early Collection IEQ/gland IEQ/g 500000 450000 400000 350000 300000 250000 200000 150000 100000 50000 0 classic early 7000 6000 5000 4000 3000 2000 1000 0 classic early

Long-term Islet Graft Function?

Cold storage Surgical manipulation Ischemia Isolation stress Chemical stress Mechanical stress Non physiologic culture environment Inadequate mass Immunosuppressive drug toxicity Inflammation Rejection Role of Isolation Enzyme?

Isolation Enzyme Collagenase bacteria Clostridium Histolyticum Sigma - crude collagenase: 6 different collagenases, aminopeptidase, clostripain, phospolipase-c & neutral proteases Roche purified collagenase -- Liberase Collagenase Type-I, Type-II and Thermolysin

Acinar ECM Is Free islets

Experimental Design Fluorescent Liberase-HI FITC conjugated Liberase-HI (Molecular Probe) Confocal Fluorescence Microscope Immuno Electron Microscope Roche Liberase + Insulin Secretory Capability Time course exposure and culture - Basal insulin secretion Stimulated Insulin Secretion - Dynamic glucose challenge and KCL stimulation Insulin C-timer [transgenic mouse] islets - visualization of proinsulin granules Islet cell expressions Adhesion molecules (CD 106 and CD 62p) Apoptotic and anti-apoptotic molecules (Bax, Bcl-2) In vivo Transplantation Graft function CD 11b deposition

Fluorescent (FITC) Conjugated Liberase-HI Mouse islets -- intraductal injection of FITC conjugated Liberase and isolation of islets (n=4 donors) Human islets -- one hour exposure of FITC conjugated Liberase in vitro (n=8 donors) Confocal Fluorescence Microscopic & Immuno Electron Microscopic Examinations Fresh islets and acinar cells 3 days cultured islets and acinar cells Epifluorescence double staining with insulin

Mouse Islet Control Mouse Acinar Control

Morphology Viability (Calcin-AM, P.I. Stain)

Beta cell Acinar cell

Human Islet Control Human Acinar Control

DTZ Viability (Calcin-AM, P.I. Stain)

G Control-Hank s exposed islet H Liberase exposed islet 2 µ 2 µ

Beta cell Acinar cell

Cultured Mouse Islet Control Control Cultured Mouse Acinar

Fresh Cultured

Beta cell Acinar cell

Effect of enzyme exposure on insulin secretion Human islets were exposed to Liberase for 15, 30, 45 or 60 minutes and washed and cultured for 60 hours basal insulin secretion (n=6donors) 1 hour exposure of human islets to Liberase Dynamic glucose challenge 1 hour exposure KCL stimulation (n=4 donors) Exposure of Insulin C-Timer Transgenic mouse islets proinsulin visualization (color change)

Insulin Secretory Defect

Insulin Secretory Defect Control Liberase Insulin Retention in Islets

Effect of enzyme exposure on islet cell expressions Human islets were exposed to Liberase for 1 hour and cultured for 60 hours (n=6 donors) islet cell attachment to the dishes adhesion molecules expressions V-CAM-1 [CD 106], P-selectin [CD 62p] apoptotic and anti-apoptotic molecules (Bax, Bcl-2) Cycloheximide (protein synthesis inhibitor) treatment prevents cell attachment and adhesion molecule expressions

Effect of enzyme exposure on transplanted islets Liberase exposed (1 h) Human islets were transplanted (n=26) 150-400 islets/graft in NODscid mice (Streptozotocin induced, renal capsule site) Graft survival and recipient survival CD11b (marker of inflammation) deposition In graft area

100 Percent Diabetes free {n=26} 75 50 25 Control Treated 0 0 5 10 15 20 post transplantation time (days)

Summary Isolation process internalizes the enzyme particles in islet and acinar cells 3 days cultured islets also contained the particles Reduction in insulin secretion correlated with time of enzyme exposure (secretory defect) Adhesion molecules were expressed and apoptotic pathways were activated in islets Enzyme exposed islets recruited intense inflammatory cells

Conclusion Isolated islets carry potentially unwanted isolation enzyme by-products and reducing the exposure to enzyme is crucial Suggestions Collection of islets in UW solution during isolation (collection phase) possibly prevents further activation of enzyme (further exposure)