Head activator and head inhibitor are signals for nerve cell differentiation in hydra

1987 ◽  
Vol 122 (1) ◽  
pp. 72-77 ◽  
Author(s):  
Sabine A.H. Hoffmeister ◽  
H.Chica Schaller
Development ◽  
1995 ◽  
Vol 121 (4) ◽  
pp. 1205-1216 ◽  
Author(s):  
B. Galliot ◽  
M. Welschof ◽  
O. Schuckert ◽  
S. Hoffmeister ◽  
H.C. Schaller

Hydra provides an interesting developmental model system where pattern formation processes are easily accessible to experimentation during regeneration. Previous studies have shown that the neuropeptide head activator affects cellular growth and head-specific cellular differentiation during head regeneration and budding. In order to investigate the signal transduction pathway and the regulatory genes involved in these processes, we measured cAMP levels after head activator treatment and found that head activator leads to an increase in cAMP levels at concentrations where effects on nerve cell determination and differentiation are observed (10(−11) to 10(−9) M). Moreover, exposure of intact hydra to a permeable form of cAMP stimulates nerve-cell differentiation and thus mimicks the effect of endogenous head activator. Band-shift assays were performed to detect changes in hydra nuclear protein binding activity during regeneration or after head activator treatment. We found that the cAMP response element (CRE) promotes a specific and strong DNA-binding activity which is dramatically enhanced and modified during early regeneration or after HA treatment. We also identified a surprisingly highly conserved hydra gene encoding the cAMP Response Element Binding protein, which is involved in this CRE-binding activity. Initiation of regeneration upon wounding provokes an endogenous release of HA which leads to the final differentiation of determined nerve cells. We propose that the nerve-cell differentiation observed within the first 4–8 hours of regeneration relies on the agonist effect of head activator on the cAMP pathway, which would in turn modulate the CRE-binding activity of the hydra CREB protein and thus regulate the transcriptional activity of genes involved in regeneration processes.


Author(s):  
Sabrina Picocci ◽  
Antonella Bizzoca ◽  
Patrizia Corsi ◽  
Thea Magrone ◽  
Emilio Jirillo ◽  
...  

2002 ◽  
Vol 80 (10) ◽  
pp. 1678-1689 ◽  
Author(s):  
Osamu Koizumi

Hydra belongs to the class Hydrozoa in the phylum Cnidaria. Hydra is a model animal whose cellular and developmental data are the most abundant among cnidarians. Hence, I discuss the developmental neurobiology of hydra. The hydra nerve net is a mosaic of neural subsets expressing a specific neural phenotype. The developmental dynamics of the nerve cells are unique. Neurons are produced continuously by differentiation from interstitial multipotent stem cells. These neurons are continuously displaced outwards along with epithelial cells and are sloughed off at the extremities. However, the spatial distribution of each neural subset is maintained. Mechanisms related to these phenomena, i.e., the position-dependent changes in neural phenotypes, are proposed. Nerve-net formation in hydra can be examined in various experimental systems. The conditions of nerve-net formation vary among the systems, so we can clarify the control factors at the cellular level by comparing nerve-net formation in different systems. By large-scale screening of peptide signal molecules, peptide molecules related to nerve-cell differentiation have been identified. The LPW family, composed of four members sharing common N-terminal L(or I)PW, inhibits nerve-cell differentiation in hydra. In contrast, Hym355 (FPQSFLPRG-NH3) activates nerve differentiation in hydra. LPWs are epitheliopeptides, whereas Hym355 is a neuropeptide. In the hypostome of hydra, a unique neuronal structure, the nerve ring, is observed. This structure shows the nerve association of neurites. Exceptionally, the tissue containing the nerve ring shows no tissue displacement during the tissue flow that involves the whole body. The neurons in the nerve ring show little turnover, although nerve cells in all other regions turn over continuously. These associations and quiet dynamics lead me to think that the nerve ring has features similar to those of the central nervous system in higher animals.


1986 ◽  
Vol 115 (1) ◽  
pp. 9-17 ◽  
Author(s):  
Thomas Holstein ◽  
Chica H. Schaller ◽  
Charles N. David

1980 ◽  
Vol 36 (6) ◽  
pp. 660-662 ◽  
Author(s):  
M. Sensenbrenner ◽  
G. G. Jaros ◽  
G. Moonen ◽  
B. J. Meyer

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