All pancreatic cell types (endocrine, exocrine, and ductal) are derived fro
m the same endodermal dorsal and ventral anlage, which grow together to for
m the definitive pancreas. Golosow and Grobstein were pioneers in the field
of pancreatic developmental research, as were Wessells and Cohen, who alre
ady in the 1960s performed classic embryological experiments describing the
morphogenesis of the pancreas and the epithelio-mesenchymal interactions t
hat are instrumental for proper pancreas development. Recent findings sugge
st that follistatin and fibroblast growth factors represent some of these k
ey mesenchymal factors that actively promote at least pancreatic exocrine d
evelopment. The true endodermal origin of the pancreatic endocrine cells be
came evident by experiments performed by the groups of LeDouarin and Rutter
in the 1970s. The newly acquired insights regarding the specification of p
ancreatic endocrine cells as controlled by the notch signaling pathway (i.e
., similar to the mechanisms by which neurons are specified during neurogen
esis) have provided a novel understanding of the long acknowledged similari
ties between neurons and the pancreatic endocrine cells. Last, the identifi
cation of a number of distinct transcription factors operating at various l
evels of pancreatic development and in different cell types has provided us
eful information both on pancreas development and on various pancreatic dis
orders such as diabetes. Interestingly, four of the hitherto defined five d
ifferent maturity-onset diabetes of the young (MODY) genes correspond to tr
anscription factors, and, in addition, several transcription factors have a
lso been linked to type 2 diabetes.