A novel cottong ovule culture: Induction, growth, and characterization of submerged cotton fibers (Gossypium hirsutum L.)

Summary The growth of submerged cotton (Gossypium hirsutum L.) fibers from cultured ovules has been investigated. The results indicate that exogenous plant hormone levels regulate the induction of submerged fiber growth. The age of ovules at induction is also important. Cell diameter, wall thickness, and cell length of submerged fibers were measured and compared with air-grown fibers and fibers grown in vivo (produced by cotton plants grown in the greenhouse). Various cellwall thickening patterns were observed among submerged fibers, while only one predominant cell-wall deposition pattern was produced in air-grown fibers and in fibers produced in vivo. The diameter of submerged fibers was about the same as that of air-grown fibers but about 22% less than that of fibers grown, in vivo. It appears that the secondary cell wall thickenings are initiated earlier in submerged fibers. The cell-wall thickness of submerged fibers, at 41 d post anthesis (DPA), was 51% greater than that of fibers grown in vivo, whereas the cell-wall thickness of air-grown fibers was 42% less than that of fibers produced in vivo. The cell length of submerged fibers was approximately half that of fibers grown in vivo. and the air-grown fiber length was about two-thirds of fibers grown in vivo. The age of ovules at induction affects the outcome of the air-grown fiber-cell length, but does not appear to affect the length of submerged fiber cells. To produce submerged fiber growth, we found that the optimal age of ovules at induction was 0 DPA, and the optimal medium (with a GA₃ of 0.5 μM and an IAA range of 5-20 μM) depends on the time of ovule induction (−2 to+2DPA). We conclude that conditions leading to submerged cotton fiber growth have great potential for (a) direct monitoring of growth and making precise, detailed measurements during fiber growth and development; (b) producing cellulose and fibers in vitro more efficiently than earlier ovule-culture methods; and (c) using these unique cultures to obtain a better understanding of signal transduction and gene expression leading to growth, development, and programmed cell death in the life history of the cotton fiber.     

Cytomorphometry of sarcoplasmic reticulum in extrinsic eye muscles of the teleost (Tinca tinca L.)

Summary The sarcoplasmic reticulum of the white and red muscle fibers in the extrinsic eye muscle of the tench (Tinca tinca L.) differs in its organization. The SR of the white fibers is organized according to the Z type, the SR of the red fibers according to the A/I type. In order to estimate the volume and surface of the SR component in both types of muscle fibers, a stereological analysis was carried out.The volume of the SR expressed as a volume density (Vv _SR) is twofold greater in the white than in the red muscle fibers. The surface of the SR, expressed as surface density (Sv _SR) is 20,5% larger in the white muscle fibers.I extend my sincerest thanks to Prof. E. R. Weibel for helpful discussion and instructions in the use of his method and to Mrs. Anna Mleczko-Michalik for skillfull technical assistance. — This work was supported by Polish Academy of Science, project number 09.4.1.4.5.     

Physical properties of polymorphic yeast prion amyloid fibers

Amyloid fibers play important roles in many human diseases and natural biological processes and have immense potential as novel nanomaterials. We explore the physical properties of polymorphic amyloid fibers formed by yeast prion protein Sup35. Amyloid fibers that conferred distinct prion phenotypes ([PSI⁺]), strong (S) versus weak (W) nonsense suppression, displayed different physical properties. Both S[PSI⁺] and W[PSI⁺] fibers contained structural inhomogeneities, specifically local regions of static curvature in S[PSI⁺] fibers and kinks and self-cross-linking in W[PSI⁺] fibers. Force-extension experiments with optical tweezers revealed persistence lengths of 1.5 μm and 3.3 μm and axial stiffness of 5600 pN and 9100 pN for S[PSI⁺] and W[PSI⁺] fibers, respectively. Thermal fluctuation analysis confirmed the twofold difference in persistence length between S[PSI⁺] and W[PSI⁺] fibers and revealed a torsional stiffness of kinks and cross-links of ∼100–200 pN·nm/rad.     

Histochemical Characterization and Distribution of Fiber Types in the Pectoralis Muscle of the Ostrich (Struthio camelus) and Emu (Dromaius novaehollandiae)

The muscle fibers of the pectoralis (M. pectoralis pars thoracicus) of a male and a female ostrich (Struthio camelus) and a male and a female emu (Dromaius novaehollandiae) were studied histochemically for succinate dehydrogenase and myofibrillar adenosine triphosphatase. Slow-tonic (ST), fast-twitch oxidative-glycolytic (FOG) and fast-twitch glycolytic (FG) fibers were approximately equal in number and distribution in the emu pectoralis examined. In the ostriches, both predominantly FG and approximately equal areas, were present. ST fibers were significantly (P ≤ 0.05) larger than the similarly (P ≥ 0.05) sized FG and FOG fibers in the female ostrich and emus. In the male ostrich ST fibers were smaller (P ≤ 0.05) than FG fibers, neither of which were significantly (P ≥ 0.05) different from FOG fibers. The ratites have the greatest percentage and widest distribution of ST fibers found in any avian pectoralis studied to date. This could represent the ancestoral avian pectoralis, neoteny or an effect of flightlessness. ST fibers are used in the maintenance of posture, which is probably the main role of the pectoralis in the emu. The predominantly FG areas of the ostrich are indicative of an additional function, namely, behavioural display. Sexual dimorphism in the ostrich pectoralis is strongly suggested.     

Characteristics of antimicrobial fibers prepared with wood periodate oxycellulose

A kind of antimicrobial fibers, a composite of Chitosan-Dialdehyde Cellulose (C-DAC) fibers, was prepared by using commercially elemental chlorine-free (ECF) bleached kraft softwood cellulose fibers oxidized by periodate and then further grafted by chitosan with different molecular weights. The characteristics of the C-DAC fibers and physical properties as well as antimicrobial activities of the handsheet made of C-DAC fibers were measured. The results show that the dry and rewet tensile indices, antimicrobial activity against Staphylococcus aureus and Escherichia coli, can be improved significantly as the molecular weight of grafted chitosan on the dialdehyde cellulose fibers decreases.     

Conduction velocities and fiber diameters in a cutaneous nerve of the pigeon

Summary The characteristics of fibers of a cutaneous nerve supplying the wing skin of the pigeon have been investigated with electrophysiological and electron microscopic techniques.Recordings of the compound action potential showed four distinct peaks with conduction velocities of about 30 m/s, 12 m/s, 4 m/s and 0.5 m/s.From electron micrographs both fiber diameters and thickness of myelin sheath were assessed and used as criteria for segregating various fiber populations. Altogether four groups could be discerned: large thickly myelinated fibers, small thickly myelinated fibers, small thinly myelinated fibers, and unmyelinated or C-fibers. The subdivision of the thickly myelinated fibers into two populations is evidenced mainly by corresponding peaks in the compound action potential. The thinly myelinated fibers with a mean diameter of 2 m contributed about 90% of all myelinated fibers in this nerve.When comparing fiber dimensions and conduction velocities of this avian nerve with those of mammalian cutaneous nerves, the lower CV's of avian nerve fibers can be explained by smaller diameters and thinner myelin sheaths.The results of this investigation are a prerequisite for latency considerations in central somatosensory pathways in birds.Abbreviations CAP compound action potential - CV conduction velocity - D fiber diameter - d axon diameter - g ratio d/D - m thickness of myelin sheath     

The Specific Force of Single Intact Extensor Digitorum Longus and Soleus Mouse Muscle Fibers Declines with Aging

In the present study we measured, for the first time, the isometric specific force (SF, force normalized to cross sectional area) generated by single intact fibers from fast- (extensor digitorum longus, EDL) and slow-twitch (soleus) muscles from young adult (2–6), middle-aged (12–14) and old (20–24 month-old) mice. SF has also been measured in single intact flexor digitorum brevis fibers from young mice. Muscle fibers have been classified into fast- or slow-twitch based on the contraction kinetics. Maximum SF recorded in EDL and soleus fibers from young and middle-aged mice did not differ significantly. A significant age-dependent decline in maximum SF was recorded in EDL and soleus fibers from young or middle-aged to old mice. The SF was 377 ± 18, 417 ± 20 and 279 ± 18 kPa for EDL fibers from young, middle-aged and old mice, respectively and 397 ± 17, 405 ± 24 and 320 ± 33 kPa for soleus fibers from age-matched mice, respectively. The frequency needed to elicit maximum force in EDL and soleus fibers from middle-aged to old mice did not differ significantly. In conclusion, the specific force developed by both fast and slow-twitch single intact muscle fibers declines with aging and more significantly in the former. Received: 14 July 2000/Revised: 7 September 2000     

Musculature in polychaetes: comparison of Myrianida prolifera (Syllidae) and Sphaerodoropsis sp. (Sphaerodoridae)

Abstract. The relationship of the polychaete taxa Syllidae and Sphaerodoridae within Phyllodocida is still unresolved: phylogenetic analyses either show them as sister groups or more widely separated. The present article aims to provide information about the structure of the muscular system that could be essential for understanding their relationship. A crucial point is whether the body wall contains circular muscles, which has recently been shown to be absent in more taxa than previously known. The F-actin filaments in members of Myrianida prolifera (Syllidae) and Sphaerodoropsis sp. (Sphaerodoridae) were labeled with phalloidin and their three-dimensional relationships reconstructed by means of confocal laser scanning microscopy. Among the noteworthy differences that emerged between the species are (1) members of M. prolifera possess four, those of Sphaerodoropsis sp. eight, longitudinal muscle strands; (2) the body wall in M. prolifera contains transverse fibers in a typical, supralongitudinal position, while in Sphaerodoropsis sp., corresponding fibers lie beneath the longitudinal strands; (3) pro- and peristomium in M. prolifera have no distinct F-actin fibers, while five longitudinal pairs and three single transverse muscular fibers shape the anterior end in Sphaerodoropsis sp.; (4) the proventricle of M. prolifera comprises primarily radial muscle fibers arranged in distinct rows, while in Sphaerodoropsis sp. the axial proboscis consists of longitudinal and circular fibers and radial fibers are lacking; (5) in M. prolifera, the proximal and distal sections of the two anteriormost pairs of dorsal cirri possess longitudinal myofilaments, which are separate from the body wall musculature; by contrast, all appendages in Sphaerodoropsis sp. do not; (6) both species have bracing muscles: in M. prolifera they are positioned above the longitudinal fibers, whereas in Sphaerodoropsis sp. they are uniquely positioned between longitudinal and sublongitudinal transverse fibers. These results do not support a sister-group relationship of Syllidae and Sphaerodoridae. In addition, Sphaerodoropsis sp. is yet another example in the list of polychaetes lacking typical circular muscles in the body wall.     

Spinal mechanisms of electric organ discharge synchronization in Gymnotus carapo

Summary The duration of the electric organ discharge (EOD) in Gymnotus carapo is brief and independent of fish size. Spinal mechanisms involved in electrocyte synchronization were explored by recording spontaneous action potentials of single fibers from the electromotor bulbospinal tract (EBST). Using the field potential of the medullary electromotor nucleus (MEN) as a temporal reference we calculated the orthodromic conduction velocity (CV) of these fibers (range: 10.7–91 m/s).The CVs (in m/s) of fibers recorded at the same level of the spinal cord were significantly different in small and large fish; this difference disappeared when CV were expressed as percentage of body length/ms. Plotting these values against conduction distance (also in %) showed that low CV fibers predominate in the rostral cord while only fast fibers are found at distal levels. Moreover, antidromic stimulation of the distal cord was only effective on high CV fibers. The orthodromic CVs in the distal portion of the recorded fibers were calculated by collision experiments; no significant differences were found between proximal and distal portions.The spatial distribution of CV values within the EBST is proposed to play the main role in synchronizing the electromotoneurons' activity along the spinal cord.Abbreviations EOD electric organ discharge - EO electric organ - EBST electromotor bulbospinal tract - MEN medullary electromotor nucleus - CV conduction velocity - EMN electromotoneuron     

Nylon-fiber affinity selection of red blood cells and tissue culture cells on the basis of cell surface determinants

Nylon fibers coated with various lectins were used for the specific selection from mixed populations of erythrocytes or tissue culture cells with lectin receptors. Binding of human group O red blood cells to fibers treated with Ulex europaeus lectin I (H-specific) or of human group A red cells to fibers treated with Helix pomatia lectin (A-specific) was proportional to lectin concentration in the solution used to adsorb lectin to the fibers. Binding was blood group specific and increased with increasing concentrations of red cells applied to the fibers. Most adsorption of lectin to the fibers occurred within minutes; cell binding to lectin-coated fibers was almost complete within 30 min. Blood group negative Chinese hamster tissue culture cells bound non-specifically to Helix-coated fibers with a frequency of less than 10⁻⁴ input cells; the yield of viable, colony-forming cells bound to PHA-coated fibers was about 1%. Epithelial cells from cultures of amniotic fluid or fetal kidney contained 1–30% cells positive for the ABO blood group of the donor; blood group positive cells from these cultures were poorly bound to fibers coated with blood group specific lectins, though they bound readily to PHA-coated fibers, suggesting that presence of appropriate surface determinants may be necessary but not sufficient for lectin: cell binding in this system.     

The cole-moore effect in nodal membrane of the frogRana ridibunda: Evidence for fast and slow potassium channels

Summary The K conductance (g _K) kinetics were studied in voltage-clamped frog nodes (Rana ridibunda) in double-pulse experiments. The Cole-Moore translation forg _K–t curves associated with different initial potentials (E) was only observed with a small percentage of fibers. The absence of the translation was found to be caused by the involvement of an additional, slow,g _K component. This component cannot be attributed to a multiple-state performance of the K channel. It can only be accounted for by a separate, slow K channel, the fast channel being the same as then ⁴ K channel inR. pipiens.The slow K channel is characterized by weaker sensitivity to TEA, smaller density, weaker potential (E) dependence, and somewhat more negativeE range of activation than the fast K channel. According to characteristics of the slow K system, three types of fibers were found. In Type I fibers (most numerous) the slow K channel behaves as ann ⁴ HH channel. In Type II fibers (the second largest group found) the slow K channel obeys the HH kinetics within a certainE range only; beyond this range the exponential decline of the slowg _K component is preceded by anE-dependent delay, its kinetics after the delay being the same as those in Type I fibers. In Type III fibers (rare) the slow K channel is lacking, and it is only in these fibers that the Cole-Moore translation of the measuredg _K–t curves can be observed directly.The physiological role of the fast and slow K channel in amphibian nerves is briefly discussed.     

Sexual dimorphism in neuronal projections from the antennae of silk moths (Bombyx mori,Antheraea polyphemus) and the gypsy moth (Lymantria dispar)

Summary The antennal lobe of both sexes of the silk moth Bombyx mori contains 55–60 ventrally located antennal glomeruli; in addition, that of the male contains a dorsal macroglomerular complex (MGC). A group of identifiable glomeruli consisting of two lateral large glomeruli (LLG) and four medial small glomeruli (MSG) is present in both sexes, but the LLG are greatly enlarged in the female. A MGC is also present in the male gypsy moth Lymantria dispar and male giant silk moth Antheraea polyphemus. The MGC in all of these species is organized into 3–4 distinct levels of glomeruli. Antennal sensory fibers were stained by cobalt backfills in B. mori, A. polyphemus, and L. dispar. Most fibers stained from cut long hairs (sensilla trichodea) projected to MGC in males and LLG in both sexes of B. mori. The distribution of fibers in the MGC of B. mori was topographically biased in that a majority of fibers from anterior branches projected medially in MGC while most fibers from posterior branches projected laterally or anteriorly. Terminal arborizations of single fibers were each restricted to a single glomerular level of the MGC. Fibers projecting to the posterior antennal center were frequently stained in cut-hair and control preparations, apparently by uptake of cobalt through intact sensilla on flagellar branches.     

Electrogenesis of embryonic chick skeletal muscle cells differentiated in vitro

Electrogenesis of embryonic chick skeletal muscle cells differentiated in monolayer cultures was investigated. Muscle fibers in vitro generate spike potentials similar to those of fibers in vivo. However, other responses, plateaux resembling those in heart muscle, are also elicited. These results suggest that a functional differentiation exists in cultured muscle fibers.     

Mechanochemical study of conformational transitions and melting of Li-, Na-, K-, and CsDNA fibers in ethanol–water solutions

Highly oriented fibers of Li-, Na-, K-, and CsDNA were prepared with a previously developed wet spinning method. The procedure gave a large number of equivalent fiber bundle samples (reference length, L₀, typically = 12–15 cm) for systematic measurements of the fiber length L in ethanol–water solutions, using a simple mechanochemical set up. The decrease in relative length L/L₀ with increasing ethanol concentration at room temperature gave evidence for the B-A transition centered at 76% (v/v) ethanol for NaDNA fibers and at 80 and 84% ethanol for K- and CsDNA fibers. A smaller decrease in L/L₀ of LiDNA fibers was attributed to the B-C transition centered at 80% ethanol. In a second type of experiment with DNA fibers in ethanol–water solutions, the heat-induced helix–coil transition, or melting, revealed itself in a marked contraction of the DNA fibers. The melting temperature T_m, decreased linearly with increasing ethanol concentration for fibers in the B-DNA ethanol concentration region. In the B-A transition region, Na- and KDNA fibers showed a local maximum in T_m. On further increase of the ethanol concentration, the A-DXA region followed with an even steeper linear decrease in T_m. The dependence on the identity of the counterion is discussed with reference to the model for groove binding of cations in B-DNA developed by Skuratovskii and co-workers and to the results from Raman studies of the interhelical bonds in A-DNA performed by Lindsay and co-workers. An attempt to apply the theory of Chogovadze and Frank-Kamenetskii on DNA melting in the B-A transition region to the curves failed. However, for Na- and KDNA the T_m dependence in and around the A-B transition region could be expressed as a weighted mean value of T_m of A- and B-DNA. On further increase of the ethanol concentration, above 84% ethanol for LiDNA and above about 90% ethanol for Na-, K-, and CsDNA, a drastic change occurred. T_m increased and a few percentages higher ethanol concentrations were found to stabilize the DNA fibers so that they did not melt at all, not even at the upper temperature limit of the experiments (～ 80°C). This is interpreted as being due to the strong aggregation induced by these high ethanol concentrations and to the formation of P-DNA. Many features of the results are compatible with the counterion–water affinity model. In another series of measurements, T_m of DNA fibers in 75% ethanol was measured at various salt concentrations. No salt effect was observed (with the exception of LiDNA at low salt concentrations). This result is supported by calculations within the Poisson–Boltzmann cylindrical cell model. © 1994 John Wiley & Sons, Inc.     

Cell lineage of flight muscle fibers in Drosophila: a fate map of the induced shibire phenotype in mosaics

Summary A blastoderm fate map has been prepared for Drosophila, using mosaics of a temperature-sensitive mutation, shibire (shi). The mutation can cause abnormal flight muscle morphology, inducible only by a short heat pulse in early metamorphosis. Thus muscle lineage and development are unperturbed until the heat pulse in the early pupa. The developmental focus of the shi muscle phenotype maps to the ventral thorax at the expected site of thoracic mesoderm, and probably indicates the blastoderm progenitors of the adult flight muscle. The fate map provides greater detail than previously available for the dorsolongitudinal fibers (DLM) of flight muscle, showing wide separation of the fibers of flight muscle. DLM fibers a and b map close together, and far anterior to fibers e and f, which also map together. On a fate map, common developmental focus indicates a common blastoderm origin. Thus, the observed pattern for DLM fibers suggests that the blastoderm progenitors for each of these syncytial fiber pairs (a, b; e, f) include only one or two cells. It follows that there is usually a single genotype within each fiber pair (a, b; e, f), and that this genotype is directly reflected in the fiber phenotype. In a large number of cases, DLM fibers a and b differ in phenotype from other DLM fibers, in parallel with their other differences (e.g., timing of development in pupa, innervation, motor activity). The separation of fate map locations of the developmental focus for DLM fibers within mesoderm suggests that specific fibers of flight muscle may, in normal development, originate in all three thoracic mesodermal parasegments.     

The adult musculature of two pseudostomid species reveals unique patterns for flatworms (Platyhelminthes,Prolecithophora)

We analyzed the adult musculature of two prolecithophoran species, Cylindrostoma monotrochum (von Graff, 1882) and Monoophorum striatum (von Graff, 1878) using a phalloidin-rhodamine technique. As in all rhabdithophoran flatworms, the body-wall musculature consisted of three muscle layers: on the outer side was a layer of circular muscle fibers and on the inner side was a layer of longitudinal muscle fibers; between them were two different types of diagonally orientated fibers, which is unusual for flatworms. The musculature of the pharynx consisted of a basket-shaped grid of thin longitudinal and circular fibers. Thick anchoring muscle fibers forming a petal-like shape connected the proximal parts of the pharynx with the body-wall musculature. Male genital organs consisted of paired seminal vesicles, a granular vesicle, and an invaginated penis. Peculiar ring-shaped muscles were only found in M. striatum, predominantly in the anterior body part. In the same species, seminal vesicles and penis only had circular musculature, while in C. monotrochum also longitudinal musculature was found in these organs. Female genital organs were only present in M. striatum, where we characterized a vagina interna, and a bursa seminalis. Transverse, crossover, and dorsoventral muscle fibers were lacking in the middle of the body and greatly varied in number and position in both species.     

Arrangement and structure of sinus hair muscles in the big-clawed shrew,Sorex unguiculatus

The arrangement and structure of sinus hair muscles in the snout of the shrew, Sorex unguiculatus, were studied by electron microscopy and serial section light microscopy. Both striated and smooth muscles are directly associated with sinus hair follicles. The striated muscle fibers originate from the base of a follicle and insert onto the superficial portion of adjoining caudally positioned follicles. Some fibers insert into the corium instead of inserting into a follicle. The fibers show a fine structure typical of red fibers. Smooth muscle cells form a network with elastic fibers beneath the corium. Some cells are directly attached to the capsule of the sinus, thus forming a type of M. arrector pili. Striated muscle fibers that appear to end in the corium are connected with the smooth muscle network through the elastic fibers which appear to function as the tendon of these two types of muscle cell.     

Evidence of a microtrabecular cytoskeletal lattice in glandular cells of hydrozoan planulae

Hydrozoan planulae of Pennaria tiarella and Podocoryne carnea were processed for transmission electron microscopy using diethylene glycol distearate (DGD). The DGD functions as a removable embedding medium to produce embedment-free sections of intact planulae. Images of glandular cells obtained using embedment-free sections were compared with those from conventional Spurr-embedded sections. In unembedded sections a large number of thin anastomosing fibers were observed throughout the cytoplasm of the glandular cell. The fibers appeared to coalesce in certain areas to form thick bundles of fibers that partitioned the glandular cytoplasm into spherical compartments. The meshwork of fibers is three-dimensional and resembles a microtrabecular lattice. Mitochondria are suspended within and attached to the network of fibers, thus suggesting a cytoskeletal role of the fibers. This study documents the presence of a cytoplasmic fiber system within cells of intact invertebrate larvae.     

The claw closer muscle of Neohelice granulata (Grapsoidea,Varunidae): a morphological and histochemical study

Longo, M.V., Goldemberg, A.L. and Díaz, A.O. 2011. The claw closer muscle of Neohelice granulata (Grapsoidea, Varunidae): a morphological and histochemical study. —Acta Zoologica (Stockholm) 92 : 126–133. The claw closer muscle of Neohelice granulata was studied according to histological, histochemical, and morphometrical criteria. Adult male crabs in intermoult stage were collected from Mar Chiquita Lagoon (Buenos Aires, Argentina). Muscle fibers show evident striations and oval‐elongated nuclei with loose chromatin. The loose connective tissue among muscle fibers consists of cells and fibers embedded in an amorphous substance. Muscle histochemistry reveals two slow fiber types: ‘A’ and ‘B’. Prevailing A fibers are larger, and they usually show, with respect to B type, a weaker reaction to whole techniques. Fibers with short (SS), intermediate (IS), and long sarcomeres (LS) appear in the claw closer muscle, being the LS fibers predominant. Concluding, the histochemical and morphometrical characteristics of the claw closer muscle fibers of N. granulata are indicative of slow fibers. The slow A type (low resistant to fatigue) prevails.