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S Berking

Publications and source records attributed to S Berking.

11 recordsLinked to original sources

The protein phosphatase inhibitor cantharidin induces head and foot formation in buds of Cassiopea andromeda (Rhizostomae, Scyphozoa).

The polyps of Cassiopea andromeda produce spindle shaped, freely swimming buds which do not develop a head (a mouth opening surrounded by tentacles) and a foot (a sticky plate at the opposite end) until settlement to a suited substrate. The buds, therewith, look very similar to the planula larvae produced in sexual reproduction. With respect to both, buds and planulae, several peptides and the phorbolester TPA have been found to induce the transformation into a polyp. Here it is shown that cantharidin, a serine/threonine protein phosphatase inhibitor, induces head and foot formation in buds very efficiently in a 30 min treatment, the shortest yet known efficient treatment. Some resultant polyps show malformations which indicate that a bud is ordinary polyp tissue in which preparatory steps of head and foot formation mutually block each other from proceeding. Various compounds related to the transfer of methyl groups have been shown to affect head and foot formation in larvae of the hydrozoon Hydractinia echinata. These compounds including methionine, homocysteine, trigonelline, nicotinic acid and cycloleucine are shown to also interfere with the initiation of the processes which finally lead to head and foot formation in buds of Cassiopea andromeda.

Alkaloids

Metamorphosis and pattern formation in Hydractinia echinata, a colonial hydroid.

There are several reasons why Hydractinia echinata Hydrozoa, Cnidaria) is excellently suited to study developmental processes. In the laboratory fertilization takes place every morning in the seawater in thousands of eggs. Cleavage starting synchronously leads to a ciliated planula larva within 2 to 3 days. Onset of metamorphosis from the larval to the polyp stage must be triggered externally. There are several agents known to induce or to interfere with induction of metamorphosis thus allowing access to the biochemical basis of this process. The pattern of the resultant polyp can be influenced by certain treatments during the process of metamorphosis allowing access to a process of proportioning. The colony develops by elongation of hollow tubes at the base of the polyps, termed stolons on which in more or less regular intervals new polyps emerge. Two (main) types of polyps are formed allowing to study spacing by lateral inhibition and lateral dependence of each other. In the present paper current data and hypotheses concerning all these topics are discussed.

Animals

Control of formation of the two types of polyps in Thecocodium quadratum (Hydrozoa, Cnidaria).

Thecocodium quadratum (Werner, Jber. Biol. Anst. Helgoland, 1965) is a colonial hydroid which produces 2 different types of polyps: gastrogonozooids and dactylozooids. The mouthless dactylozooids bear tentacles and catch the prey, which is then taken over and swallowed by the gastrogonozooids which have no tentacles. It is obvious that for a colony to survive both polyps must exist simultaneously arranged in a certain spatial pattern. Our experiments indicate that the formation of polyps in a growing culture is governed by at least 3 principles: (1) short range inhibition between polyps irrespective of their differentiation; (2) long range specific inhibition between gastrogonozooids; and (3) long range supporting influence (lateral help, Meinhardt, H., Models of Biological Pattern Formation, 1982) between gastrogonozooids and dactylozooids.

Animals

Homarine (N-methylpicolinic acid) and trigonelline (N-methylnicotinic acid) appear to be involved in pattern control in a marine hydroid.

A morphogenetically active compound has been isolated from tissue extract of Hydractinia echinata and identified to be N-methylpicolinic acid (homarine). When applied to whole animals, homarine prevents metamorphosis from larval to adult stage and alters the pattern of adult structures. The concentration of homarine in oocytes is about 25 mM. During embryogenesis, metamorphosis and early colony development the overall homarine content does not change. Adult colonies contain a fourfold lower homarine concentration than larvae. The polyp's head contains twofold more homarine than the gastric region and the stolons. A second, similarly active compound, N-methylnicotinic acid (trigonelline), has also been identified in Hydractinia tissue at concentrations about one-third that of homarine. Incubation of larvae in 10 to 20 microM-homarine or trigonelline prevents head as well as stolon formation. If the compounds are applied in a pulse during metamorphosis, a large part of the available tissue forms stolons. Since microM concentrations of homarine and trigonelline are morphogenetically active, whereas mM concentrations are present in the tissue it appears that both substances are stored within the tissue.

Alkaloids

Commitment of stem cells to nerve cells and migration of nerve cells precursors in preparatory bud development in Hydra.

Budding in Hydra starts as an evagination of the double-layered tissue in the parent animal's gastric region. Five hours later the density of nerve cells in the bud's tissue doubles, representing the first detectable difference from the cellular composition of the surrounding tissue. These new nerve cells derive from multipotent stem cells which are in S-phase one day before evagination starts. Some of the bud's new nerve cells derive from stem cells which have migrated into the future bud's tissue after their commitment, apparently attracted by the bud anlage. The bud anlage recruits precursors of nerve cells even during starvation, during which nerve cell production ceases in other parts of the body. Furthermore, the bud anlage controls the duration of the development from commitment to final differentiation of the resulting nerve cells. Experiments with an inhibitor purified from hydra tissue indicate a tight correlation between stages of preparatory bud development and stages of recruitment of nerve cells for the bud. Whether or not precursors of nerve cells are involved in the control of bud formation in normal hydra, as compared to epithelial hydra which still bud though consisting of epithelial cells only, will be discussed.

Animals

Control of nerve cell formation from multipotent stem cells in Hydra.

Feeding of starved animals provides a very short signal which determines stem cells to differentiate into nerve cells after the next mitosis. Only those stem cells become determined which are just in the middle of their S-phase at the time of feeding. Stem cells of any other stage of the cycle do not become determined. Nerve cell determination is suppressed by very low concentrations of an endogenous inhibitor. The inhibitor exerts its effect only during the first half of the S-phase, not before and not after this period. Based on these finding it is proposed that stem cells are susceptible to 2 different signals during the first half of their S-phase; one signal allows the development into nerve cells, the other prevents this development. Within this period the decision whether to become a nerve cell or not is reversible. It becomes fixed at the end of this period.

Animals