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Xu, X., D’Hoker, J., Stange, G., Bonne, S., De Leu, N., Xiao, X., Van de Casteele, M., Mellitzer, G., Ling, Z., Pipeleers, D., Bouwers, L., Scharfmann, R., Gradwohl, G. and Heimberg, H. (2008) Beta Cells Can Be Generated from Endogenous Progenitors in Injured Adult Mouse Pancreas. Cell, 132, 197-207.
http://dx.doi.org/10.1016/j.cell.2007.12.015

has been cited by the following article:

• TITLE: Differentiation of Pancreatic Ductal Epithelial Cells into Insulin Like Cell Clusters in Chronic Pancreatitis

  AUTHORS: Pondugala Pavan Kumar, Gaddipati Radhika, G. Venkat Rao, D. Nageshwar Reddy, M. Sasikala

  KEYWORDS: Chronic Pancreatitis, Ductal Epithelial Cells, Islet Like Clusters, Cell Differentiation

  JOURNAL NAME: Open Journal of Endocrine and Metabolic Diseases, Vol.5 No.12, December 14, 2015

  ABSTRACT: Background/Aim: Islet regeneration in chronic pancreatitis (CP) is relevant for managing the associated loss of endocrine function. Because ductal epithelial cells were earlier demonstrated to differentiate into pancreatic endocrine mass, we evaluated their proliferation and differentiation in chronic pancreatitis. Methods: Pancreatic ducts were obtained from surgically resected pancreata of 12 patients with chronic pancreatitis and 15 control subjects. CK19 positive ductal cells were evaluated for their proliferating and differentiating abilities upon immunostaining with Ki 67 and hormone positivity for insulin and glucagon, apart from monitoring Pdx 1 expression. Results: In comparison to the controls, a greater number of proliferating pancreatic ductal epithelial cells (PDECs) were observed under conditions of CP. The increase in Pdx1 expressing PDECs (22%) and proliferating Pdx1 expressing PDECs (30%) was significant (P βcell mass adjacent to the ducts increased by 28%.Conclusion: Enhanced capability of PDECs to proliferate and differentiate into endocrine mass suggests that PDECs form a source of progenitors for cell based therapy in chronic pancreatitis.