Transdifferentiation of macrophages into fibroblasts as a result of Schistosoma mansoni infection

The possibility of transdifferentiation of macrophages into fibroblasts which could be at the origin of fibrotic tissue in schistosome-infected mice was studied using immunocytochemical techniques. Macrophage cell samples extracted from the peritoneal cavity of schistosome-infected mice were fractionated on a Percoll gradient. The cultures were purified by treatment with a trypsin solution to eliminate any fibroblasts possibly collected along with the macrophages. Immunocytochemical methods were then used to characterize the cells at different points in time. The fibroblastic property of the morphologically transformed cells was confirmed by their positive labeling with the anti-procollagen antibody. However, these cells still possessed the mac-1 and mac-2 antigens which characterize the monomacrophage line.SCOPUS: ar.jinfo:eu-repo/semantics/publishe

A study of peritoneal cells from healthy and Schistosoma mansoni-infected mice with special reference to myofibroblasts arising in culture.

Adherent, trypsin-resistant, peritoneal cells from mice with chronic schistosomiasis mansoni, and from control mice, were cultivated in vitro up to 20 days. Fibroblasts regularly appeared, about 6 days after seeding, in cultures of the manyfold more numerous cells from infected mice, concomitantly with a dramatic increase, detected by autoradiography, in the percentage of DNA-replicating cells of the monocyte-macrophage lineage. Peritoneal cells from healthy and from infected mice were fractionated on discontinuous Percoll gradients. Eight cell subsets were harvested in both cases, quantitated, and studied by electron microscopy. Two fractions (2 and 3: 1.041 < densities < 1.060 g/ml) from infected mice were greatly enriched in monoblasts and promonocytes. The cells of the different subsets were seeded separately, trypsin-treated and cultivated in vitro. Cultures of cell fractions 2 and 3 from infected mice contained the majority of the DNA-synthesizing cells and gave regularly rise to fibroblasts. Cultures of the different fractions were used for sequential morphological observations (2-11 days) at the electron microscope level. Early cultures were also used for the ultrastructural detection of the Mac-1 (CD 18/CD 11b) surface antigen by gold immunocytochemistry. A few fibroblasts were rarely observed in cultures of fractions 2 and 3 from control mice, while cells with ultrastructural features of myofibroblasts were regularly observed in cultures of the same fractions harvested from mice with chronic schistosomiasis. Fractions 2 and 3 from infected mice contained a large number of Mac-1 positive monoblasts. The correlations between the presence of monoblasts, DNA replication in cells of the monocyte-macrophage lineage and the appearance of myofibroblasts in cultures of the same fractions derived from infected mice are discussed.SCOPUS: ar.jinfo:eu-repo/semantics/publishe

Morphology and dynamics of calcium carbonate granules produced by different earthworm species.

Granules of calcium carbonate produced by earthworms are regularly found in soil profiles, but little is known of their origins and dynamics. Pure cultures of a range of species were therefore set up, using artificial soils, and the granules recovered for examination. Species of Lumbricus, Aporrectodea, Octolasion and Allolobophora all produced granules larger than 0.125mm, but Eisenia hortensis did not. For comparison, two compost-dwelling Eisenia species were also cultured. These yielded no granules at all, suggesting that the genus as a whole does not produce granules, consistent with its lack of calciferous sacs. Granules recovered from the other 7 species have a variety of sizes and morphologies, ranging from single calcite crystals to aggregations up to 2.5mm in diameter. SEM photographs of the granules and data on granule concentrations in relation to depth are presente