Author:
Schubert Undine,Lehmann Susann,Schmid Janine,Morawietz Henning,Bornstein Stefan R.,Ludwig Barbara
Abstract
AbstractIntraportal islet transplantation in patients with type 1 diabetes enables
restoration of glucose-regulated insulin secretion. However, several factors
hamper a widespread application and long-term success: chronic hypoxia, an
inappropriate microenvironment and suppression of regenerative and proliferative
potential by high local levels of immunosuppressive agents. Therefore, the
identification of alternative and superior transplant sites is of major
scientific and clinical interest. Here, we aim to evaluate the adrenal as an
alternative transplantation site. The adrenal features a particular
microenvironment with extensive vascularization, anti-apoptotic and
pro-proliferative, anti-inflammatory and immunosuppressive effects. To validate
this novel transplantation site, an in vitro co-culture system of adrenal cells
and pancreatic islets was established and viability, islet survival, functional
potency and antioxidative defense capacity were evaluated. For in vivo
validation, an immune-deficient diabetic mouse model for intra-adrenal islet
transplantation was applied. The functional capacity of intra-adrenally grafted
islets to reverse diabetes was compared to a standard islet transplant model and
measures of engraftment such as vascular integration were evaluated. The
presence of adrenal cells positively impacted on cell metabolism and oxidative
stress. Following transplantation, we could demonstrate enhanced islet function
in comparison to standard models with improved engraftment and superior
re-vascularization. This experimental approach allows for novel insights into
the interaction of endocrine systems and may open up novel strategies for islet
transplantation augmented through the bystander effect of other endocrine cells
or the active factors secreted by adrenal cells modulating the
microenvironment.
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