Accordingly, our results can reinforce the idea of the protective role of tunic morula/compartment cells. Microscopic observations on C. intestinalis indicate the presence of intratunical bacteria and alga-like cells [30] and [47]. Unicellular algae seem to be restricted
to certain periods and to be related to the environment in which animals live. As regards bacteria, it is still unclear whether they are symbiotic PR-171 mouse or pathogenic, or whether they are stable and seasonally dependent. Since they are found both in the matrix and within phagocytic features in some tunic cells, there may be a defense system against bacterial infection or against some groups of bacteria. At present there is no ecological and taxonomic information on the bacteria found in the Ciona tunic, and it is still unclear by which
mechanisms they can survive in the tunic. Further investigations of their fine structure and further efforts to clarify their role are needed. The present observations disclose an involvement of particular cell types in the production of AMPs in the inflamed tunic. Infiltration of hemocytes induced in C. intestinalis upon injection of sheep erythrocytes into the tunic increases significantly the number of cells in the area of entry; most of them are in a degenerative state and undergo drastic changes so it is difficult to identify all cell types on the basis of their ultrastructural
aspects. The release Diflunisal of their content which could take part in the destruction http://www.selleckchem.com/products/ch5424802.html of the foreign cells, may be judged by the presence of gold particles labeling the cellular remnants and granules significantly positive to Ci-MAM-A and Ci-PAP-A. AMPs are released into the extracellular space, upon the activation of degranulation processes. Variously distributed in the tunic matrix of the inflamed area are electron-dense particles which can be clustered and packed, or be interspersed among degranulating cells to form irregular masses; associated with them we localized the natural molecules Ci-MAM-A and Ci-PAP-A. Concerning ‘inflammatory hemocytes’ in the hemocoel we expect an increased expression of AMP genes. The next major objective is the elucidation of the distribution and the rate of synthesis of these molecules in circulating hemocytes during an inflammation. In conclusion, our data clearly demonstrate for the first time that AMPs are also synthesized in the tunic cells of C. intestinalis, and give further evidences that these peptides constitute an important part in host defense against invading microbes. However, the complex interactions leading from recognition of invaders via signal transduction to induction of AMP genes needs further investigation. First author is indebted to Prof.