Abstract
Macrophagescanaccumulateonthesurfaceofemptyandislet-containingalginatecapsules,leadingtolossoffunctionaltissue.Inthisstudy,theeffectofperitonealmacrophagedepletiononthebiocompatibilityofalginatemacrocapsulesandfunctionofmacroencapsulatedporcineneonatalpancreaticcellclusters(NPCCs)wasinvestigated.ClodronateliposomeswereinjectedintotheperitonealcavitiesofnormoglycemicLewisrats5and2daysbeforethetransplantation.EmptyorNPCC-containingCa-alginatepolyL-lysine(PLL)-coatedmacrocapsulesweretransplantedintotheperitonealcavitiesofratsinjectedwitheitherclodronateliposomesorsaline.Ondays7,14and21,sampleswereevaluatedbyimmunohistochemistryforcellularimmuneresponsesonthesurfaceofthemacrocapsulesandformacrophagepopulationsinomentaltissue.ToassessthefunctionofmacroencapsulatedNPCCs,insulinsecretoryresponsestoglucoseandtheophyllineweremeasuredaftercapsuleretrieval.Insaline-injectedcontrolgroups,alloftheemptyandNPCC-containingmacrocapsuleswereovergrownwithmacrophages,thisbeingespeciallysevereonNPCC-containingmacrocapsules.Intheclodronateliposomes-injectedgroup,themajorityoftheemptymacrocapsuleswerefreeofmacrophageaccumulationandtheNPCC-containingmacrocapsuleswerelessovergrownthanincontrolanimals.HigherinsulinresponsestoglucoseandtheophyllinewereobservedinNPCCsretrievedfromratsinjectedwithclodronateliposomes.WeconcludethatdepletionofperitonealmacrophageswithclodronateliposomesimprovethesurvivalofmacroencapsulatedNPCCs.
PMID:12694544[Pubmed-MEDLINE]