The importance of turbellarians in the marine meiobenthos: a review

Recent data and opinions on meiofaunal ecology are briefly reviewed; and from scattered data, the place of turbellarians in the meiobenthic community is discussed. Turbellarian diversity, density, and biomass are higher in sandy habitats than in muddy bottoms. In sand, turbellarian diversity is of the same magnitude as that of other important meiofaunal taxa, while densities range between 7–25% of the total meiofauna. Mean individual turbellarian dry weight seems to be four times that of nematodes and in sandy habitats turbellarian biomass may be equal to or excede that of nematodes. Most turbellarian species may be considered as predators and in this respect may take the place occupied by macrofaunal species in muddy sediments. mens.

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Symbiosis between a pelagic flatworm and a dinoflagellate from a tropical area: structural observations

A morphological account on the endosymbiosis between Amphiscolops sp and Amphidinium sp is given, based on scanning and transmission electron microscopy observations. The algal symbionts (15–20 µm in diameter) are found among cells of the peripheral parenchyma. Amphidinium sp. has a single pyrenoid of the multiple-stalked type, with several chloroplast lobes radiating from it. A comparison with A. klebsii is made. Our observations reinforce the assumption of selectivity of Amphiscolops for the symbiotic genus Amphidinium.     

Frontal organs in the Acoelomorpha (Turbellaria): Ultrastructure and phylogenetic significance

Using characters discernible through electron microscopy, we redefine the organ traditionally identified as the frontal organ in acoelomorph turbellarians as being a collection of two to several large mucus-secreting glands whose necks emerge together through a frontal pore at the exact apical pole of the body, i.e. at the point where the pattern of epidermal ciliary rootlets converges. Representatives that we have studied of each of the acoel families Paratomellidae, Diopisthoporidae, Solenofilomorphidae, Convolutidae, Otocelidae, and Mecynostomidae, as well as a representative of the Nemertodermatida, have such glands. Up to five additional types of glands that open anteriorly outside of the frontal pore, some of which are indistinguishable from glands of the general body wall, could be seen in the nemertodermatid, in Hesiolicium inops (Paratomellidae), and in representatives of the latter four acoel families. In Paratomella, three different types of glands open in diffuse fashion in a frontal glandular complex reminiscent of that in the Macrostomida.Sensory elements near the frontal pore appear to be independent of the gland necks, and so the organ cannot be considered a sensory organ.The frontal organ, as described above, appears very likely to be homologous within the Acoelomorpha, and represents another strong (although unrooted) autapomorphy for this line of turbellarian evolution.     

Old and new records of turbellarians from the central areas of Spain

From the point of view of its biodiversity, the Iberian Peninsula is one of the most interesting areas. Its special geographical location and geological history have created a high degree of diversity within the invertebrates groups in general, and within the ecological group of the Turbellaria in particular. In the present work, old and new records of turbellarian species from the central areas of the Iberian Peninsula are presented. Data on their biology and distribution within the freshwater habitats, mainly limnic, are also provided. This study is mainly based on the project Fauna Iberica III. This revised version was published online in July 2006 with corrections to the Cover Date.     

Ultrastructure of the copulatory stylet and accessory spines in Haplopharynx quadristimulus (Turbellaria)

The copulatory organ of Haplopharynx quadristimulus Ax, 1971 (Carolina form, Rieger, 1977) consists of a proximal prostatic vesicle and a distal stylet apparatus comprising a central tubular stylet and four to five peripheral accessory spines. By electron microscopy it could be seen that the stylet and spines were intracellular specializations. The copulatory organ can be interpreted as a specialization of an epithelial canal extending from the testes to the body wall. In the complex stylet apparatus, the epithelium was differentiated into six cell types. The stylet, which was formed in a matrix syncytium next to the prostatic vesicle, extended into the lumen of the stylet canal. The interior of the stylet apparatus contained one group of cells that had thick ciliary rootlets and another that had rootlet-like ribbons.The cells that contain the rootlets enveloped bundles of longitudinally arranged muscles. The accessory spines were formed in cells which lay peripheral to the muscle bundles. The spines, stylet, rootlet-like ribbons, and rootlets had similar patterns of periodic cross striations. The similarity in striation patterns suggests that the accessory spines and stylet are composed of modified ciliary rootlets.     

Ultrastructural features of cocoon-shell globules in the vitelline cells of neoophoran platyhelminths

The Neoophora is characterized by the presence of complex female gonads composed of both germaria and vitellaria. The vitellaria are made up of vitelline cells that differentiate to produce and accumulate reserve substances (proteins, lipid, glycogen) and precursors of the egg capsule or cocoon shell (phenolic proteins). A comparative ultrastructural and cytochemical investigation of shell-forming globules from the vitelline cells of some neoophoran platyhelminths shows that the internal structures of the shellforming globules can be grouped into two (or three) main types. In the first, globule content is characterized by a more or less homogeneous electron-dense substructure evidently arising from repeated coalescence of small vesicles produced by the rough endoplasmic reticulum and Golgi complex. A variant of this type of globule shows intermingling (or concentric) electron-dense and translucent areas producing a pattern resembling brain convolutions (convoluted pattern). The second type of shell-globule structure shows a multigranular pattern, presumably resulting from repeated fusions of Golgian vesicles followed by incomplete coalescence of the electron-dense content. Comparison of shell-globule structure in different taxa could be useful in elucidating some complex and still-unclear phylogenetic relationships among Platyhelminthes.     

Phosphorylation of phosphofructokinase from skeletal muscle: correlations between phosphorylation and muscle function.

The specific radioactivity of [³²P]-phosphate incorporated into muscle phosphofructokinase was in equilibrium with the specific radioactivity of the γ-phosphate group of ATP. The incorporation was independent of the presence of cycloheximide. The total content of covalently bound phosphate in phosphofructokinase was correlated with the functional state of the muscle from which the enzyme was purified. Muscle dissected post mortem led to phosphofructokinase containing less than 2 phosphate groups per tetramer. Muscle dissected in vivo gave phosphofructokinase with 4 phosphates per tetramer when kept at rest and 8 phosphates per tetramer when stimulated to contract.     

An ultrastructural study of mitotic division in differentiated gastric smooth muscle cells

Summary An ultrastructural examination of tissue from the gizzards of chicks just before and just after hatching showed numerous mitotic divisions in the well differentiated and functional smooth muscle. The nuclei in the very elongate, dividing cells were located centrally. The cytoplasm immediately adjacent to the nuclei contained the normal fully differentiated complement of myofilaments. During the active stages of division, after the breakdown of the nuclear membrane, myofilaments were shown to lie between the individual chromosomes. The process of division only occupied a small portion of the long muscle cells; the ultrastructural changes seen appeared similar to those described in other cell types.This work was supported by grants from the National Heart Foundation of Australia and the Australian Research Grants Committee. Part of this study was completed while J.L.S.C. was in receipt of a Queen Elizabeth II Research Fellowship. T. B. was supported by a Commonwealth Postgraduate Award.     

Development and characterization of primary cultures of smooth muscle cells from the fibromuscular stroma of the guinea pig prostate

Summary Primary cultures of smooth muscle cells (SMCs) were obtained by a two-step enzymatic digestion of guinea pig prostatic stroma. Ultrastructural morphology and growth characteristics of these cells conformed to those reported for SMCs isolated from vascular and visceral tissue sources. Electron microscopic examination indicated that the cells assumed modified myofibroblastoid features in culture. Microfilaments with associated dense bodies were markedly depleted in cultured smooth muscle cells, in comparison with those of the parent tissue. Cultured cells also possessed increased content of rough endoplasmic reticulum indicating the increased secretory or protein-synthetic capacity of the cells. Immunoperoxidase staining for cytoskeletal markers using monoclonal antibodies to desmin and vimentin supported the ultrastructural observations, suggesting a decline in desmin-staining intermediate filaments during “modulation” to the myofibroblastoid form. Despite this depletion of smooth muscle-specific differentiation markers and reversion to more general mesenchymal properties, the cells retained the ability to contract on challenge with norepinephrine, and grew in the characteristic “hill and valley” pattern on attaining confluence. Inasmuch as the estrogen and androgen receptor expression of the parent stromal tissue is also retained, these primary cell cultures should provide a useful model to study regulation of prostatic development. This work was supported by research grants from the National Health and Medical Research Council of Australia, the Anti Cancer Foundation of the Universities of South Australia, and the Flinders Medical Centre Research Foundation.     

Culture and characterization of fetal human atrial and ventricular cardiac muscle cells

Summary Atrial and ventricular cardiac muscle cells isolated from 14- to 18-wk old fetal human hearts were grown in culture and characterized. Once established in culture the flattened cells contracted spontaneously and possessed differentiated ultrastructural characteristics including organized sarcomeres, intercalated discs, and transverse tubules with couplings. Atrial granules were present in the cultured atrial cells. Some cultured ventricular myocytes also contained electron-dense granules associated with Golgi cisternae, which were similar in size and appearance to atrial granules. The cultured ventricular myocytes divided and expressed the genes for thymidine kinase, histone H4, myosin heavy chain, muscle-specific creatine kinase, atrial natriuretic factor, and insulin-like growth factor II. These results establish that differentiated fetal human heart muscle cells can be cultured in sufficient quantities for biochemical, molecular, and morphological analyses. This work was supported by a postdoctoral fellowship from the American Heart Association, Louisiana Affiliate (JBD) and the National Institutes of Health, Bethesda, MD (HL-35632) (WCC).     

Precocious in vitro development of satellite cells from dystrophic chicken muscle

Summary Satellite cells, liberated from pectoral muscle of juvenile dystrophic chickens by sequential treatment with collagenase, hyaluronidase, and trypsin and preplated to remove fibroblasts and cultured on gelatin proliferated rapidly, fused and formed confluent muscle cultures within 6 d in vitro with minimal contamination by fibroblasts. When identical isolation and culturing techniques were applied to muscle from age-mateched normal chickens proliferation and differentiation were slower, contamination with fibroblasts was much greater, and only a small number of myotubes were formed. After injection of the myotoxic anesthetic marcaine into normal pectoral muscle for 5 consecutive days, myotube formation was accelerated in satellite cell cultures, but the rate of differentiation was not as rapid as that occurring in cells from dystrophic muscle. This research was supported by a grant from the Muscular Dystrophy Association of Canada.     

Structure and function of the spermathecal complex in the phlebotomine sandflyPhlebotomus papatasi Scopoli (Diptera: Psychodidae): I. Ultrastructure and histology

Females of phlebotomine sandflies (Diptera: Psychodidae) possess highly variable spermathecae that present several important taxonomic characters. The cause of this diversity remains a neglected field of sandfly biology, but may possibly be due to female post-mating sexual selection. To understand this diversity, a detailed study of the structure and function of the spermathecal complex in at least one of the species was a prerequisite. Using scanning and transmission electron microscopy, described here is ultrastructure of the spermathecal complex in the sand fly,Phlebotomus papatasi Scopoli. The spermathecal complexes are paired; each consists of a long spermathecal duct, a cylindrical spermathecal body, and a spherical spermathecal gland. Muscle fibres, nerves, tracheoles, and vascular sinuses connect the spermathecal body and duct through the epithelial layers. Spermathecal gland is formed by a typical insect epidermis and consisting of an epithelial layer of class-1 epidermal cells and elaborate glandular cells of class-3 epidermal cells, each having both receiving and conducting ductules (i.e. “end apparatus”) and a “cytological apodeme”, which is a newly described cell structure. The spermathecal body and duct are lined by class-1 epidermal cells and a cuticle, and are enveloped by a super-contracting visceral muscular system. The cuticle consists of rubber-like resilin, and its fibrillar arrangement and chemical nature are described. A well-developed neuromuscular junction exists between the spermathecal gland and the spermathecal body, which are connected to each other by a nerve and a muscle. The spermathecal complexes of the sandfly are compared with those of other insect species. The physiological role and possible evolutionary significance of the different parts of spermathecal complex in the sandfly are inferred from the morphology and behaviour. Post-mating sexual selection may be responsible for the structural uniqueness of the spermathecal complex in phlebotomine sandflies.     

Ultrastructure of midgut endocrine cells in the adult mosquito, Aedes aegypti

The ultrastructure of endocrine cells in the midgut of the adult mosquito, Aedes aegypti, resembled that of endocrine cells in the vertebrate gastro-intestinal tract. Midgut endocrine cells, positioned basally in the epithelium as single cells, were cone-shaped and smaller than the columnar digestive cells. The most distinctive characteristic of endocrine cells was numerous round secretory granules along the lateral and basal plasma membranes where contents of the granules were released by exocytosis. Secretory granules in each individual cell were exclusively of one type, either solid or 'haloed', and for all cells observed, the range in granule diameter was 60-120 nm. The cytoplasm varied in density from clear to dark. Lamellar bodies were prominent in the apical and lateral cellular regions and did not exhibit acid phosphatase activity. The basal plasma membrane was smooth adjacent to the basal lamina, whereas in digestive cells the membrane formed a labyrinth. Some endocrine cells reached the midgut lumen and were capped by microvilli; a system of vesicles and tubules extended from beneath the microvilli to the cell body. An estimated 500 endocrine cells were distributed in both the thoracic and abdominal regions of the adult midgut. In one midgut, we classified a sample of endocrine cells according to cytoplasmic density and granule type and size; endocrine cells with certain types of granules had specific distributions within the midgut.     

Isolation and culture of smooth muscle cells from human umbilical cord arteries

Summary A short method is described for obtaining a large number of pure vascular smooth muscle cells in culture. The smooth muscle cells were isolated from human umbilical cord arteries digested twice by an enzyme mixture of collagenase, trypsin, elastase, and DNAase with addition of α-tosyl-lysyl chloromethane. Primary cell culture and first subculture were not contaminated by endothelial cells, no Factor VIII being produced. The cultures consisted of smooth muscle cells as appeared from phase contrast and electron microscopy. Part of this study was supported by a scholarship from the Dutch Ministry of Education and Science and by the Leyden University Foundation.     

On the nature of pharyngeal muscle cells in the Tardigrada

As part of a transmission electron microscopic study of the embryological development in tardigrades, the ultrastructure of the pharynx was examined. The intent was to establish whether the pharyngeal muscle cells constitute an eclodermal myoepithelium (as in many aschelminth pharynges) or whether they are mesodermal (as in certain other aschelminth groups and among articulates). In the latter case the cuticle would be produced solely by specialized epithelial cells. The eutardigrade species Halobiotus crispae Kristensen, 1982, was investigated in four embryological stages, as a newly hatched juvenile, in the active adult stage, and in the hibernation stage pseudosimplex I. A comparison was made with the arthrolardigrade Actinarctus doryphorus Schulz, 1935, in the active adult stage and in the simplex stage. The results indicate that the tardigrade pharynx is an ectodermal myoepithelium. The muscles appear to be truly cross-striated and monosarcomerial. The phylogenetic implications of these findings are discussed briefly.     

Increased adipogenicity of cells from regenerating skeletal muscle

Adipose tissue development is observed in some muscle pathologies, however, mechanisms that induce accumulation of this tissue as well as its cellular origin are unknown. The adipogenicity of cells from bupivacaine hydrochloride (BPVC)-treated and untreated muscle was compared in vitro. Culturing cells from both BPVC-treated and untreated muscles in adipogenic differentiation medium (ADM) for 10 days resulted in the appearance of mature adipocytes, but their number was 3.5-fold higher in cells from BPVC-treated muscle. Temporal expressions of PPARgamma and the presence of lipid droplets during adipogenic differentiation were examined. On day 2 of culture in ADM, only cells from BPVC-treated muscle were positive both for PPARgamma and lipid droplets. Pref-1 was expressed in cells from untreated muscle, whereas its expression was absent in cells from BPVC-treated muscle. In ADM, the presence of insulin, which negates an inhibitory effect of Pref-1 on adipogenic differentiation, was required for PPARgamma2 expression in cells from untreated muscle, but not for cells from BPVC-treated muscle. These results indicate that BPVC-induced degenerative/regenerative changes in muscle lead to increased adipogenicity of cells, and suggest that this increased adipogenicity not only involves an increase in the number of cells having adipogenic potential, but also contributes to the progression of these cells toward adipogenic differentiation.     

Isolation and enrichment of skeletal muscle progenitor cells from mouse bone marrow

There is great interest in the therapeutic potential of non-hematopoietic stem cells obtained from bone marrow called mesenchymal stem cells (MSCs). Rare myogenic progenitor cells in MSC cultures have been shown to convert into skeletal muscle cells in vitro and also in vivo after transplantation of bone marrow into mice. To be clinically useful, however, isolation and expansion of myogenic progenitor cells is important to improve the efficacy of cell transplantation in generating normal skeletal muscle cells. We introduced into MSCs obtained from mouse bone marrow, a plasmid vector in which an antibiotic (Zeocin) resistance gene is driven by MyoD and Myf5 enhancer elements, which are selectively active in skeletal muscle progenitor cells. Myogenic precursor cells were then isolated by antibiotic selection, expanded in culture, and shown to differentiate appropriately into multinucleate myotubes in vitro. Our results show that using a genetic selection strategy, an enriched population of myogenic progenitor cells, which will be useful for cell transplantation therapies, can be isolated from MSCs.     

ATP-dependent potassium channels of muscle cells: Their properties,regulation, and possible functions

ATP-dependent potassium channels are present at high density in the membranes of heart, skeletal, and smooth muscle and have a lowP _open at physiological [ATP]_i. The unitary conductance is 15–20 pS at physiological [K⁺] _o , and the channels are highly selective for K⁺. Certain sulfonylureas are specific blockers, and some K channel openers may also act through these channels. K_ATP channels are probably regulated through the binding of ATP, which may in turn be regulated through changes in the ADP/ATP ratio or in pH_i. There is some evidence for control through G-proteins. The channels have complex kinetics, with multiple open and closed states. The main effect of ATP is to increase occupancy of long-lived closed states. The channels may have a role in the control of excitability and probably act as a route for K⁺ loss from muscle during activity. In arterial smooth muscle they may act as targets for vasodilators.     

Quantitative and qualitative in vitro analysis of the stem cell potential of hematopoietic cells purified from murine skeletal muscle

The murine skeletal muscle contains hematopoietic stem cells, but this potential has so far not been studied quantitatively or qualitatively in vitro. To quantify the hematopoietic stem cell potential, we have used highly purified SP/CD45^＋ cells in long-term culture initiating cell （LTC-IC） assays. The SP/CD45^＋ cell population purified from murine muscle was found to have significant stem cell activity with an LTC-IC frequency of 1/640. Single-cell-sorted SP/CD45^＋ cells from muscle exhibited robust proliferative activity in vitro at day 16 （380-fold amplification）, especially after culture with OP-9 layers that also support embryonic stem cells. Amplified cell populations originating from single cells exhibited multilineage differentiation ability with evidence of myeloid, lymphoid and NK cell markers. Thus, our results demonstrate that hematopoietic stem cells that can be quantified by LTC-IC assays exist in the murine skeletal muscle and show also for the first time, at the single-cell level, that these cells exhibit multilineage differentiation ability and major proliferative potential.