Fibrin supports human fetal islet-epithelial cell differentiation via p70 s6k and promotes vascular formation during transplantation

Authors

Matthew Riopel, Children's Health Research Institute, London, ON
Jinming Li, Children's Health Research Institute, London, ON
Mark Trinder, Children's Health Research Institute, London, ON
George F. Fellows, Western University
Rennian Wang, Children's Health Research Institute, London, ONFollow

Document Type

Article

Publication Date

8-30-2015

Journal

Laboratory Investigation

Volume

95

Issue

8

First Page

925

Last Page

936

URL with Digital Object Identifier

10.1038/labinvest.2015.74

Abstract

The human fetal pancreas expresses a variety of extracellular matrix (ECM) binding receptors known as integrins. A provisional ECM protein found in blood clots that can bind to integrin receptors and promote β cell function and survival is fibrin. However, its role in support of human fetal pancreatic cells is unknown. We investigated how fibrin promotes human fetal pancreatic cell differentiation in vitro and in vivo. Human fetal pancreata were collected from 15 to 21 weeks of gestation and collagenase digested. Cells were then plated on tissue-culture polystyrene, or with 2D or 3D fibrin gels up to 2 weeks, or subcutaneously transplanted in 3D fibrin gels. The human fetal pancreas contained rich ECM proteins and expressed integrin αVβ3. Fibrin-cultured human fetal pancreatic cells had significantly increased expression of PDX-1, glucagon, insulin, and VEGF-A, along with increased integrin αVβ3 and phosphorylated FAK and p70 s6k. Fibrin-cultured cells treated with rapamycin, the mTOR pathway inhibitor, had significantly decreased phospho-p70 s6k and PDX-1 expression. Transplanting fibrin-mixed cells into nude mice improved vascularization compared with collagen controls. These results suggest that fibrin supports islet cell differentiation via p70 s6k and promotes vascularization in human fetal islet-epithelial clusters in vivo.