Abstract

IntroductionAcute pancreatitis (AP) is one of the most common diseases involving necrotic inflammation. Bone marrow mesenchymal stem cells (BMMSCs) have the potential of multi-directional differentiation and self-renewal for tissue repair. It remains less clear if granulocyte colony-stimulating factor (G-CSF) can improve the therapeutic effect of BMMSC transplant in AP. Therefore, we explored this issue in a rat model of experimental AP.ResultsTransplanted PKH26-positive BMMSCs were present in the injured pancreatic tissue, with some cells co-expressed pancreatic cellular markers, including Pax-4, Ngn3 and Nkx-6. Pathological, biochemical and serological data suggested an improvement in histological and functional recovery in these animals relative to control. Overall, the AP model rats received BMMSCs and G-CSF co-treatment showed better recovery in terms of tissue regeneration and blood biochemical levels relative to other groups.Materials and MethodsBMMSCs from donor rats were labeled with the fluorescent dye PKH26 and transfused into recipient rats with AP induced by L-arginine. The animals were divided into a control group, and groups treated with BMMSCs, G-CSF, and BMMSCs together with G-CSF. Therapeutic effects were evaluated histologically with immunohistochemistry and immunofluorescence, together with biochemical measurement of pancreatic markers.ConclusionG-CSF therapy with BMMSC transplantation improves histological and functional outcomes in rats with experimental AP.

Highlights

  • Acute pancreatitis (AP) is one of the most common diseases involving necrotic inflammation

  • Transplanted PKH26-positive Bone marrow mesenchymal stem cells (BMMSCs) were present in the injured pancreatic tissue, with some cells co-expressed pancreatic cellular markers, including Pax-4, Ngn3 and Nkx-6

  • The cells showed the antigenic profile of BMMSCs [22]

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Summary

Introduction

Acute pancreatitis (AP) is one of the most common diseases involving necrotic inflammation. Bone marrow mesenchymal stem cells (BMMSCs) have the potential of multi-directional differentiation and self-renewal for tissue repair. It remains less clear if granulocyte colony-stimulating factor (G-CSF) can improve the therapeutic effect of BMMSC transplant in AP. We explored this issue in a rat model of experimental AP. Mesenchymal stem cells (MSCs) have the potential to differentiate into bone, cartilage, or adipose tissue under suitable conditions [10, 11]. These www.impactjournals.com/oncotarget non-hematopoietic stromal progenitor cells have selfrenewal ability and high plasticity.

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