Lineage-specific morphogenesis in the developing pancreas: role of mesenchymal factors

Development ◽  
1996 ◽  
Vol 122 (2) ◽  
pp. 439-447 ◽  
Author(s):  
G.K. Gittes ◽  
P.E. Galante ◽  
D. Hanahan ◽  
W.J. Rutter ◽  
H.T. Debase

Pancreatic organogenesis has been a classic example of epitheliomesenchymal interactions. The nature of this interaction, and the way in which endocrine, acinar and ductal cell lineages are generated from the embryonic foregut has not been determined. It has generally been thought that mesenchyme is necessary for all aspects of pancreatic development. In addition islets have been thought to derive, at least in part, from ducts. We microdissected 11-day embryonic mouse pancreas and developed several culture systems for assays of differentiation: (i) on transparent filters; (ii) suspended in a collagen I gel; (iii) suspended in a basement membrane rich gel; (iv) under the renal capsule of an adult mouse. Epithelia were grown either with or without mesenchyme, and then assayed histologically and immunohistochemically. Epithelium with its mesenchyme (growth systems i-iv) always grew into fully differentiated pancreas (acinar, endocrine, adn ductal elements). In the basement membrane-rich gel, epithelium without mesenchyme formed ductal structures. Under the renal capsule of the adult mouse the epithelium without mesenchyme exclusively formed clusters of mature islets. These latter results represent the first demonstration of pure islets grown from early pancreatic precursor cells. In addition, these islets seemed not to have originated from ducts. We propose that the default path for growth of embryonic pancreatic epithelium is to form islets. In the presence of basement membrane constituents, however, the pancreatic analage epithelium appears to be programmed to form ducts. Mesenchyme seems not to be required for all aspects of pancreatic development, but rather only for the formation of acinar structures. In addition, the islets seem to form from early embryonic epithelium (which only express non-acinar genes). This formation occurs without any specific embryonic signals, and without any clear duct or acinus formation.

2021 ◽  
Author(s):  
Yosuke Miyachi ◽  
Miki Nishio ◽  
Junji Otani ◽  
Shinji Matsumoto ◽  
Akira Kikuchi ◽  
...  

1964 ◽  
Vol 2 (3) ◽  
pp. 444
Author(s):  
J. F. A. P. Miller ◽  
S. M. A. Doak ◽  
A. M. Cross
Keyword(s):  

2008 ◽  
Vol 319 (2) ◽  
pp. 555
Author(s):  
Ipsita Dey-Guha ◽  
Mahua Mukhopadhyay ◽  
Heiner Westphal

1997 ◽  
Vol 45 (1) ◽  
pp. 107-118 ◽  
Author(s):  
André Nadeau ◽  
Gilles Grondin ◽  
Richard Blouin

ZPK is a recently described protein serine/threonine kinase that has been originally identified from a human teratocarcinoma cell line by the polymerase chain reaction and whose function in signal transduction has not yet been elucidated. To investigate the potential role of this protein kinase in developmental processes, we have analyzed the spatial and temporal patterns of expression of the ZPK gene in mouse embryos of different gestational ages. Northern blot analysis revealed a single mRNA species of about 3.5 KB from Day 11 of gestation onwards. In situ hybridization studies demonstrated strong expression of ZPK mRNA in brain and in a variety of embryonic organs that rely on epithelio-mesenchymal interactions for their development, including skin, intestine, pancreas, and kidney. In these tissues, the ZPK mRNA was localized primarily in areas composed of specific types of differentiating cells, and this expression appeared to be upregulated at a time concomitant with the onset of terminal differentiation. Taken together, these observations raise the possibility that the ZPK gene product is involved in the establishment and/or maintenance of a fully cytodifferentiated state in a variety of cell lineages.


Cell ◽  
1980 ◽  
Vol 22 (3) ◽  
pp. 719-726 ◽  
Author(s):  
Victor P. Terranova ◽  
David H. Rohrbach ◽  
George R. Martin

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