Serum-Free and Xenobiotic-Free Preservation of Cultured Human Limbal Epithelial Cells

Aim/Purpose of the Study

To develop a one-week storage method, without serum and xenobiotics, that would maintain cell viability, morphology, and phenotype of cultured human limbal epithelial sheets.

Materials and Methods

Human limbal explants were cultured on intact human amniotic membranes for two weeks. The sheets were stored in a hermetically sealed container at 23°C in either a serum-free medium with selected animal serum-derived compounds (Quantum 286) or a xenobiotic-free medium (Minimal Essential Medium) for 4 and 7 days. Stored and non-stored cultures were analyzed for cell viability, amniotic membrane and epithelial sheet thickness, and a panel of immunohistochemical markers for immature cells (ΔNp63α, p63, Bmi-1, C/EBP∂, ABCG2 and K19), differentiated cells (K3 and Cx43), proliferation (PCNA), and apoptosis (Caspase-3).

Results

The cell viability of the cultures was 98 ± 1% and remained high after storage. Mean central thickness of non-stored limbal epithelial sheets was 23 ± 3 μm, and no substantial loss of cells was observed after storage. The non-stored epithelial sheets expressed a predominantly immature phenotype with ΔNp63α positivity of more than 3% in 9 of 13 cultures. After storage, the expression of ABCG2 and C/EBP∂ was reduced for the 7 day Quantum 286-storage group; (P = 0.04), and Bmi-1 was reduced after 4 day Quantum 286-storage; (P = 0.02). No other markers varied significantly. The expression of differentiation markers was unrelated to the thickness of the epithelia and amniotic membrane, apart from ABCG2, which correlated negatively with thickness of limbal epithelia (R = -0.69, P = 0.01) and ΔNp63α, which correlated negatively with amniotic membrane thickness (R = -0.59, P = 0.03).

Conclusion

Limbal epithelial cells cultured from explants on amniotic membrane can be stored at 23°C in both serum-free and xenobiotic-free media, with sustained cell viability, ultrastructure, and ΔNp63α-positivity after both 4 and 7 days.     

Model study of muscle spindle primary endings subjected to dynamic fusimotor activation

An earlier proposed model of the de-efferented muscle spindle mechano-receptors has been developed further to simulate the effects of the dynamic fusimotor ( _D) activation of the group Ia afferents (primary endings).The rate sensitivity of the original second order receptor model might be increased simply by increasing the overall viscous damping of the simulated polar regions of the nuclear bag fibre. However, adequate simulation of the typical time course of the stretch response of the primary endings during _D-activation required a subdivision of the polar regions into an active and a passive part. A reasonable behaviour of the model was obtained by simulating a local contraction covering about 50–90% of the polar regions of the nuclear bag fibres.The ramp response of the model showed a quick rate response component that increased by increasing the rate of the simulated stretch. This component was not significantly influenced by the simulated _D-activation.A slow rate component appeared to increase approximately in the same proportion as the intensity of the simulated _D-activation.The behaviour of the model closely corresponds to that of the biological prototype. The study demonstrates that the electrophysiological effects of activating the dynamic fusimotor fibres are indeed compatible with peripheral mechanical events associated with contraction phenomena within the polar regions of the nuclear bag intrafusal muscle fibres.     

A second order mechanical model of muscle spindle primary endings

Summary With reference to experimental data and the failure of earlier proposed first order linear models of mammalian muscle spindles, a second order mechanical model of de-efferented primary endings is studied. The model takes into account the presence of two different types of intrafusal muscle fibres in a complete spindle organ. It further allows the incorporation of different gain of the mechano-electric conversion into a depolarization of the sensory terminals innervating the two types of fibres.It is shown that a closer approximation to the behaviour of the biological prototype is obtained if the transducer gain of the branch corresponding to the nuclear bag intrafusal fibres is chosen significantly higher than that corresponding to the nuclear chain branch.The marked nonlinear behaviour of muscle spindle primary endings as recently reported by Matthews and Stein (1968, 1969) is interpreted as a saturation effect of the high gain mechano-electric transducer of the nuclear bag branch. The saturation is considered to reflect a condition of complete depolarization of these sensory terminals. If a higher transducer gain actually is present, a complete depolarization of these terminals would occur at a lower degree of mechanical deformation than for the nuclear chain terminals. The mechano-electric transducer system of the nuclear chain fibres might thus behave approximately linearly within a larger range of input amplitudes. The greatly reduced gain of the primary endings at large emplitudes of imposed muscle vibrations as observed experimentally (Matthews and Stein, 1968, 1969) may thus be accounted for by the transducer gain of the nuclear chain fibres alone.List of Symbols Used C Viscous stiffness, or electrical capacitance - f Frequency of a signal - K Static gain of a system - k Elastic stiffness - R Electrical resistance - s The Laplace operator - H(s) General transfer function of a system - X (s) Laplace transform of the difference between instantanous and resting length of the complete intrafusal muscle fibre, according to the suggested model shown in Fig. 2 - (s) Laplace transform of the length of the elastic component of the proposed Maxwell branch of the sensory region of the model - (s) Laplace transform of the difference between instantanous and resting length of the lumped model of the polar (non-sensory) region of the intrafusal fibres - (s) Laplace transform of the length of the purely elastic branch of the model - The transducer gain of the output from the -branch relative to that of the -branch - v(s) Laplace transform of the total output signal (s) + (s) - Time constant defined by or =RC for the mechanical and the electrical system respectively - Angular frequency equal to 2f - Rate constant describing the relation between the lead and the lag time constant of a first order lead-lag filter network     

Antibodies to Corynebacterium Pseudotuberculosis in Adult Goats from a Naturally Infected Herd

Serum samples taken in 3 successive years (1977, 1978 and 1979) from adult dairy goats (Norwegian breed) originating from 1 herd were examined for antibodies to Gorynebacterium pseudotuberculosis. Both bacterial agglutination test (BAT) and hemolysis inhibition test (HIT) were used. The proportion of seropositive goats increased 10–12 % during the investigation period. In 1979 all animals were seropositive to BAT and about 95 % had antihemolysins in their sera. Twenty-two of the 23 one-year old goats recruited to the herd in 1978 were seropositive. The average age-specific titres increased up to the age of 3 years, and subsequently decreased for goats aged 4–7 years. Caseous lymphadenitis is thus regarded as a chronic infection. The effect of age on the titre values was significant at the 5 % level in 1977 and 1978 when HIT was used and in 1978 when BAT was used. During the investigation period the same 36 and 40 goats were examined every year by BAT and HIT, respectively. Intermediate to high correlations between titre values for the same goats from year to year were found. Both BAT and HIT are suitable for sero-epidemiological investigations concerning infection with G. pseudotuberculosis in goats.     

RAPHIDOPHYCEAE [CHADEFAUD EX SILVA] SYSTEMATICS AND RAPID IDENTIFICATION: SEQUENCE ANALYSES AND REAL‐TIME PCR ASSAYS1

Species within the class Raphidophyceae were associated with fish kill events in Japanese, European, Canadian, and U.S. coastal waters. Fish mortality was attributable to gill damage with exposure to reactive oxygen species (peroxide, superoxide, and hydroxide radicals), neurotoxins, physical clogging, and hemolytic substances. Morphological identification of these organisms in environmental water samples is difficult, particularly when fixatives are used. Because of this difficulty and the continued global emergence of these species in coastal estuarine waters, we initiated the development and validation of a suite of real‐time polymerase chain reaction (PCR) assays. Sequencing was used to generate complete data sets for nuclear encoded small‐subunit ribosomal RNA (SSU rRNA; 18S); internal transcribed spacers 1 and 2, 5.8S; and plastid encoded SSU rRNA (16S) for confirmed raphidophyte cultures from various geographic locations. Sequences for several Chattonella species (C. antiqua, C. marina, C. ovata, C. subsalsa, and C. verruculosa), Heterosigma akashiwo, and Fibrocapsa japonica were generated and used to design rapid and specific PCR assays for several species including C. verruculosa Hara et Chihara, C. subsalsa Biecheler, the complex comprised of C. marina Hara et Chihara, C. antiqua Ono and C. ovata, H. akashiwo Ono, and F. japonica Toriumi et Takano using appropriate loci. With this comprehensive data set, we were also able to perform phylogenetic analyses to determine the relationship between these species.     

Hyperferritinemia is associated with insulin resistance and fatty liver in patients without iron overload

Objective

During the last 10 years we have experienced an increasing number of referrals due to hyperferritinemia. This is probably due to increased awareness of hereditary hemochromatosis, and the availability of a genetic test for this condition. Most of these referred patients were over-weight middle-aged men with elevated ferritin levels, but without the hemochromatosis-predisposing gene mutations. We evaluated the relationship between hyperferritinemia and the metabolic syndrome in 40 patients.

Methods

Forty consecutive patients referred for hyperferritinemia were investigated. The examination programme included medical history, clinical investigation and venous blood samples drawn after an overnight fast. This resulted in 34 patients with unexplained hyperferritinemia, which were further examined. Liver biopsy was successfully performed in 29 subjects. Liver iron stores were assessed morphologically, and by quantitative phlebotomy in 16 patients.

Results

The majority of the patients had markers of the metabolic syndrome, and 18 patients (52%) fulfilled the IDF-criteria for the metabolic syndrome. Mean body mass index was elevated (28,8±4,2), mean diastolic blood pressure was 88,5±10,5 mmHg, and mean fasting insulin C-peptide 1498±539 pmol/l. Liver histology showed steatosis and nuclear glycogen inclusions in most patients (19 out of 29). Only four patients had increased iron stores by histology, of which two could be explained by alcohol consumption. Fourteen of 16 patients normalized ferritin levels after phlebotomy of a cumulative blood amount corresponding to normal iron stores. Ferritin levels were significantly related to insulin C-peptide level (p<0.002) and age (p<0.002).

Conclusion

The present results suggest that liver steatosis and insulin resistance but not increased iron load is frequently seen in patients referred for suspected hemochromatosis on the basis of hyperferritinemia. The ferritin level seems to be positively associated to insulin resistance.     

Genomic representations using concatenates of Type IIB restriction endonuclease digestion fragments

We have developed a method for genomic representation using Type IIB restriction endonucleases. Representation by concatenation of restriction digests, or RECORD, is an approach to sample the fragments generated by cleavage with these enzymes. Here, we show that the RECORD libraries may be used for digital karyotyping and for pathogen identification by computational subtraction.     

Development of real-time PCR assays for rapid detection of Pfiesteria piscicida and related dinoflagellates

Pfiesteria complex species are heterotrophic and mixotrophic dinoflagellates that have been recognized as harmful algal bloom species associated with adverse fish and human health effects along the East Coast of North America, particularly in its largest (Chesapeake Bay in Maryland) and second largest (Albermarle-Pamlico Sound in North Carolina) estuaries. In response to impacts on human health and the economy, monitoring programs to detect the organism have been implemented in affected areas. However, until recently, specific identification of the two toxic species known thus far, Pfiesteria piscicida and P. shumwayae (sp. nov.), required scanning electron microscopy (SEM). SEM is a labor-intensive process in which a small number of cells can be analyzed, posing limitations when the method is applied to environmental estuarine water samples. To overcome these problems, we developed a real-time PCR-based assay that permits rapid and specific identification of these organisms in culture and heterogeneous environmental water samples. Various factors likely to be encountered when assessing environmental samples were addressed, and assay specificity was validated through screening of a comprehensive panel of cultures, including the two recognized Pfiesteria species, morphologically similar species, and a wide range of other estuarine dinoflagellates. Assay sensitivity and sample stability were established for both unpreserved and fixative (acidic Lugol's solution)-preserved samples. The effects of background DNA on organism detection and enumeration were also explored, and based on these results, we conclude that the assay may be utilized to derive quantitative data. This real-time PCR-based method will be useful for many other applications, including adaptation for field-based technology.     

Avoidance Responses to Infrasound in Downstream Migrating European Silver Eels, Anguilla anguilla

In an attempt to develop an efficient acoustic fish fence, we have designed an infrasound source able to generate large nearfield particle acceleration. The source generates water movements by means of two symmetrical pistons in an air-filled cylinder with 21cm bore. The pistons are driven by eccentric coupling to an electric motor, with 5cm p.p. amplitude. The piston movements are 180° out of phase. The piston reaction forces are thus opposed, leading to vibration free operation. The submergible infrasound source is operated freely suspended in the water mass. The emitted sound frequency is 11.8Hz. The particle acceleration is about 0.01ms^–2 at a distance of 3m, corresponding to the threshold intensity for deterring effects of infrasound on Atlantic salmon smolts. The sound source was employed to test the effect of intense infrasound on migrating European silver eels. Fish confined in a tank displayed startle behaviour and prolonged stress reactions, telemetrically monitored as tachycardia, in response to intense infrasound. The field tests were carried out in the River Imsa. A trap that catches all the descending eels is installed near the river mouth. The trap was separated in four equal sections. During the periods with infrasound exposure, the proportion of silver eels entering the section closest to the sound source was reduced to 43% of the control value. In the section closest to the opposite river bank, infrasound increased the proportion of trapped eels to 144% of the control values. This shift of the migrating eels away from the infrasound source was highly significant.