Modulation of cytokine responses of murine CD8+ αβ intestinal intraepithelial lymphocytes by IL-4 and IL-12

The immune responses of the intestine mucosa feature the noninflammatory type, such as IgA production and oral tolerance. Th2 type cytokines have been implicated in the induction of these noninflammatory responses. In the present study, cytokine responses of CD8+ and CD4+ TCR+ intestinal intraepithelial lymphocyte ( iIEL) subsets to TCR stimulation under the influence of IL-12, IL-4, or CD28 costimulation were examined. IL-12 enhanced production of IL-10 and IFN- by the CD8+ iIEL significantly but only marginally affected the CD8+ subset, whereas IL-4 induced IL-4, IL-5, and IL-10 production and augmented TGF- production by both subsets. CD28 costimulation induced production of Th2 cytokines by CD4+ iIEL in the absence of exogenous IL-4. Unlike lymph node CD4+ cells, the CD28 costimulation-induced Th2 differentiation of CD4+ iIEL was not inhibited by IFN-. These results demonstrate active cytokine production by CD4+, CD8+, as well as CD8+ iIEL. The Th2-skewed cytokine profile of CD8+ iIEL and the IFN--resistance of Th2 differentiation of the CD4+ iIEL suggest that both iIEL subsets contribute to the induction of noninflammatory mucosal immune responses.     

Flexibility on the karyotype evolution in bitterlings (Pisces, Cyprinidae)

In bitterlings (Acheilognathinae) C- and Ag-banding karyotypes of 6 species-subspecies collected in China and South Korea were analyzed. The chromosomal constitution of 2n=46 (4SM+42ST) in Rhodeus atremius fangi was quite different from that of 2n=48 (8M+20SM+20ST) in other species-subspecies in Rhodeus. It was concluded from the analysis of banded chromosomes that the increase in number of ST during the karyotype change from 2n=48 to 2n=46 was achieved by a series of pericentric inversions from 24 M-SM to 24 ST, and the decrease in the diploid number was caused by an additional tandem fusion of 4 ST chromosomes, forming a new ST pair in the 2n=46 karyotype. The karyotype of Tanakia koreensis, T. signifer, and Acheilognathus macropterus is 2n=48 (8M+20SM+20ST), 2n=48 (8M+20SM+14–16ST+4–6 A), 2n=44 (14M+16SM+14ST), respectively. In R. ocellatus ocellatus, T. koreensis, T. signifer and A. macropterus, karyotype changes from 2n=48 to 2n=44 due to centric fusion and inversion have also been estimated. It was suggested that C-banding heterochromatin was greatly concerned with the karyotype evolution in bitterlings.     

Etude du phytochrome des graines de Pinus nigra Arn par spectrophotométrie bichromatique in vivo

Summary Phytochrome photoconversions P_rP_fr and P_frP_r can be measured by differential spectrophotometry in dry seeds (6% water content) of Pinus nigra Arn. A red light irradiation given before imbibition induces germination when the seeds are subsequently wetted and kept in darkness.In continuous darkness the phytochrome content shows a drastic increase at the beginning of moistening.The detectable pigment is entirely in the P_r form. The normal P_frP_r dark reversion is observed. P_fr destruction does not take place.     

Effect of genotype,explant and medium onin vitro regeneration of red pepper

In vitro plant regeneration was achieved inCapsicum praetermissum, C. baccatum andC. annuum cvs. G4, Bhiwapuri Sweet pepper, Cayenne pepper and Hybrid pepper. Shoots were induced from hypocotyl, cotyledon and leaf explants on Murashige and Skoog medium supplemented with 5.7 M indoleacetic acid (IAA)+13.3 M benzyladenine (BA); 22 M BA; and 44 M BA. Analysis of variance revealed that the most significant effect on shoot regeneration was due to the explant and it accounted for 56.3% of total variation observed. The genotype x explant effect on regeneration was minor relative to all other 2- and 3-way interactions because leaf explants consistently regenerated more shoots than hypocotyls or cotyledons in all the genotypes and thereby reduced the variation among the genotypes. Explant x medium interaction revealed that 22 M BA was the best growth regulator supplement in regeneration medium for optimal shoot regeneration from leaf explants. Rooting of regenerated shoots was achieved on 5.7 M IAA-containing medium, and the rooting response was better from shoots induced on medium fortified with 5.7 M IAA plus 13.3 M BA. Complete plantlets with diploid chromosome number (2n=2x=24) were transferred to soil and 60–70% of these plantlets survived and grew well.     

Methods for measuring the properties of the turbulence in bubble flow

Summary A constant temperature hot film anemometer has been used to evaluate mean liquid flow velocity, bubble frequency, turbulence scale and intensity, and the rate of energy dissipation by liquid phase bubble flow.Symbols M mass - L lenght - T time - a gas/liquid interfacial area L² - a=a/V_L specific gas/liquid interfacial area with regard to the volume of the liquid L^–1 - d bubble diameter L - d mean bubble diameter L - d_e dynamic equilibrium (maximum stable) bubble size L - d_p primary bubble diameter L - d_s Sauter bubble diameter L - E specific energy dissipation rate with regard to the volume of the liquid ML^–1T^–3 - E V_L energy dissipation rate ML²T^–3 - E=E/ since =1 g cm^–3, E has the same numerical value as E. Therefore, the symbol E is used everywhere in the present paper for E and called energy dissipation rate (S. s^–2=Stokes. s^–2) L²T^–3 - E_G or _G local relative gas hold up L²T^–3 - f() autocorrelation function [Eq. (10)] L²T^–3 - f(r) cross correlation function [Eq. (11)] L²T^–3 - g acceleration of gravity LT^–2 - k constant LT^–2 - k_L mass transfer coefficient LT^–1 - k_La volumetric mass transfer coefficient with regard to the volume of the liquid T^–1 - N₀ number of crossings of u and T^–1 - n_B bubble frequency T^–1 - r distance between two points 1 and 2 of the cross correlation function L - t time T - u momentaneous liquid velocity LT^–1 - mean liquid velocity LT^–1 - mean square fluctuation velocity L²T^–2 - intensity of turbulence LT^–1 - x position coordinate L - V volume of the bubbling layer in the column L³ - V_L volume of the bubble free layer in the column L³ - V electrical voltage (in Fig. 2) L³ - v velocity scale [Eq. (6)] LT^–1 - We_crit critical Weber number [Eq. (4)] LT^–1 - w_SG superficial gas velocity LT^–1 - w_SL superficial liquid velocity LT^–1 - _G or E_G local relative gas hold up LT^–1 - smallest scale [Eq. (6)] L - time delay in the autocorrelation function [Eq. (10)] T - energy dissipation scale [E. (15)] L - _f: Taylor's vorticity scale [E. (14)] L - kinematic viscosity of the liquid L²T^–1 - density of the liquid ML^–3 - surface tension MT^–2 - dynamic pressure of the turbulence [Eq. (8)] ML^–1T^–2 - p primary (at the aerator) - e equilibrium (far from the aerator)     

Truncated presequences of mitochondrial F1-ATPase β subunit from Nicotiana plumbaginifolia transport CAT and GUS proteins into mitochondria of transgenic tobacco

The mitochondrial F₁-ATPase subunit (ATPase-) of Nicotiana plumbaginifolia is nucleus-encoded as a precursor containing an NH₂-terminal extension. By sequencing the mature N. tabacum ATPase-, we determined the length of the presequence, viz. 54 residues. To define the essential regions of this presequence, we produced a series of 3 deletions in the sequence coding for the 90 NH₂-terminal residues of ATPase-. The truncated sequences were fused with the chloramphenicol acetyl transferase (cat) and -glucuronidase (gus) genes and introduced into tobacco plants. From the observed distribution of CAT and GUS activity in the plant cells, we conclude that the first 23 amino-acid residues of ATPase- remain capable of specifically targeting reporter proteins into mitochondria. Immunodetection in transgenic plants and in vitro import experiments with various CAT fusion proteins show that the precursors are processed at the expected cleavage site but also at a cryptic site located in the linker region between the presequence and the first methionine of native CAT.     

Physiologic aspects of pyridine nucleotide regulation in mammals

Summary Tissue levels of NAD⁺ appear to be regulated primarily by the concentration of extracellular nicotinamide, which in turn is controlled by the liver in a hormone-sensitive manner. Hepatic regulation involves the conversion of excess serum nicotinamide to Storage NAD⁺ and inactive excretory products, and the replenishment of serum nicotinamide by the hydrolysis of Storage NAD⁺. Tryptophan and nicotinic acid contribute to Storage NAD⁺, and thus are additional sources of nicotinamide. In response to administered nicotinamide, there is a preferential utilization of ATP and PRPP (5-phosphorylribose-1-pyrophosphate) for the biosynthesis of NAD⁺. This biosynthetic priority, whose purpose appears to be the conservation of intracellular nicotinamide, may explain why nicotinamide inhibits RNA and DNA synthesis in regenerating tissues and why elevated nicotinamide levels are toxic to growing animals and to mammalian cells in culture.     

Evidence for the induction of two types of potentially lethal damage after exposure of plateau phase Chinese hamster V79 cells toγ-rays

Summary The fixation of-rays induced potentially damage (PLD) caused after treatment either with-araA or in medium made hypertonic by the addition of sodium chloride was studied in plateau phase chinese hamster V79 cells. Treatment with-araA was found to affect a sector of PLD, the fixation of which specifically reduced the shoulder width of the survival curve. The effect was maximized when cell survival reached levels corresponding to an exponential line, with a slope similar to the final slope of the survival curve of untreated cells. This effect was achieved by a four hour treatment with-araA at concentrations above 150µM. Longer treatment times or incubation at higher-araA concentrations did not significantly enhance the effect. Treatment in hypertonic medium, on the other hand, enhanced cell killing in a concentration dependent (NaCl-concentration) way and the survival reached values much lower than those corresponding to an exponential line. No indication for a plateau in the effect, indicating complete fixation of the sector of PLD that reacts sensitively to this treatment, was obtained. Both the slope and the shoulder width of the survival curve were affected, the slope first being increased after short treatment times (up to 10 min), followed by a decrease in the shoulder width after longer treatment times (longer than 10 min). Lesions fixed after treatment with-araA were repaired within four hours, whereas the repair of lesions fixed after treatment in hypertonic medium (460 mM NaCl, 30 min) appeared to be biphasic, with a fast component (completed in about one hour) correlated with a decrease in the slope and a slow component (completed in four hours) correlated with restoration of the shoulder width. Based on these results, we suggest that two types of PLD may be induced in plateau phase V79 cells after exposure to-rays. One, the repair of which is completed within about one hour and which affects the slope of the survival curve, and a second, the repair of which takes place in a few hours and which specifically affects the survival curve shoulder width. The terms-PLD and-PLD are suggested for the first and second component, respectively.Comparison of the repair rates of-PLD as measured with the help of-araA and of sublethal damage as measured in split-dose experiments indicated that these two cellular repair processes have very similar kinetics when measured under the same experimental conditions. Furthermore, the rate was identical at which the shoulder of the survival curve reappeared (shoulder width was the only parameter of the survival curve affected in this type of experiment) in the time interval between either a conditioning dose of-rays and subsequent graded doses or between irradiation and treatment with-araA. Based on these results it is suggested that-PLD and sublethal damage may have a common molecular base.This work was supported by PHS-grants number CA 33951 and CA 39938 awarded by NCI, DHHS     

Effects of the growth regulator 4PU-30 on growth,K+ content,and alkaloid production in tobacco callus cultures

Growth, K⁺ content, and alkaloid production were compared in nonorganogenetic callus cultures ofNicotiana tabacum cv. Burley 21 grown at 25°C in the dark on two different media: a basal medium with 1 M -naphthaleneacetic acid and 1 M kinetin, and one with 1 M -naphthaleneacetic acid and 1 M 4PU-30 (N-(2-chloro-4-pyridyl)-N-phenylurea). These callus tissues behaved differently not only in growth and K⁺ content but also in alkaloid production. In comparison to cultures grown with kinetin, those grown with 4PU-30 showed a significantly higher fresh weight and dry weight and K⁺ content during the growth period studied. The data clearly indicate a positive correlation between K⁺ uptake rate stimulated by 4PU-30 and cell enlargement rate. However, the alkaloid biosynthesis in the callus tissues was activated by the supply of kinetin and diminished by that of 4PU-30. It thus appears that cellular enlargement of meristematic tissue stimulated by 4PU-30 limited alkaloid production.     

N-Terminal pyrazinones: a new class of peptide-bound advanced glycation end-products

Summary. The reaction of peptide Gly-Ala-Phe with the -dicarbonyl compounds glyoxal and methylglyoxal was studied under physiological conditions (pH=7.4, 37°C). Using HPLC with UV and fluorescence detection, a rapid derivatization of the peptide and the concomitant formation of well-defined products were observed. The products, which showed characteristic UV absorbance (_max=320 to 340nm) and fluorescence (_ex=330 to 340nm, _em=395 to 405nm), were identified by ESI-MS and NMR spectroscopic analysis as the N-terminally pyrazinone-modified peptides I (N-[2-(2-oxo-2H-pyrazin-1-yl)-propyl]-phenylalanine) and II (N-[2-(5-methyl-2-oxo-2H-pyrazin-1-yl)-propionyl]-phenylalanine). Model experiments revealed that the reactivity of the N-termini of peptides towards a derivatization by glyoxal is in the same order of magnitude as that of arginine, which generally is attributed as main target for -dicarbonyl compounds in proteins. Incubation of insulin with glyoxal proved the protein-bound formation of pyrazinones, with the N-terminus of the B-chain as the main target. According to these results, we conclude that N-terminal pyrazinones represent a new type of advanced glycation end-products (AGEs) with significance for biological systems and foods.     

Amplification and latency in photoreceptors: Integrated or separated phenomena?

It is shown that the models for the transduction process in photoreceptors which treat latency and amplification as integrated phenomena (integrated models) yield time scales for single photon signals (quantum bumps) which distinctly conflict with the experimentally observed ones for the ventral nerve photoreceptor of Limulus: the ratio of bump duration/ latency t _B/t _lat is predicted by integrated models to be 3 in contrast to the experimental result of 0.5. Moreover, integrated models lead to a predicted value of an extinction rate of 50%, i.e., 50% of the absorbed photons should be expected to cause no signal in the dark adapted state of the cell. In this paper it is shown that separation of latency and amplification in such a way that the latency causing process precedes amplification in the transduction process eliminates these discrepancies. In addition, the separate modeling of latency and amplification resolves the rather large ambiguity in determining the exponent n of the initial signal current J(t) ⁿreported in the literature to be between n2 (from noise analysis) up to n17 (from flash experiments). Two alternative models for the latency part of transduction are suggested which give a qualitatively much better agreement with the experimental histograms of latencies.List of Symbols A quantum bump amplitude, maximum of quantum bump signal current - latency criterion as a fraction in terms of J _max - E energy of the stimulating flash - g conductance of a single light-regulated channel - I(t) light intensity of the stimulating flash as a function of time - J(t) response current of photoreceptors to light flashes under voltage clamp - J _max maximum signal current response signal - J _min minimum current above which the signal current becomes distinguishable from the base line noise - k rate constant in models separating latency from amplification - L ligand in ligand binding model - rate constant of exponential bump decay - m number of amplification steps following gainless latency process in models separating latency and amplification - n exponent in the initial behaviour J(t)t ⁿ - Q net charge transfer of quantum bump signal current - (t) first-passage time probability density - t _B duration of quantum bump response - t _lat latency time - t _max time to peak for quantum bumps - t _r rise time for quantum bumps - U U-U _L, U=clamp voltage, U _L=reversal potential of light-regulated channels - v amplification factor - X _k intermediate conformations in transduction models This work was supported by Deutsche Forschungsgemeinschaft (SFB 160)     

Mutational spectrum induced in Saccharomyces cerevisiae by the carcinogen N-2-acetylaminofluorene

The spectrum of mutations induced by the carcinogen N-2-acetylaminofluorene (AAF) was analysed in Saccharomyces cerevisiae using a forward mutation assay, namely the inactivation of the URA3 gene. The URA3 gene, carried on a yeast/bacterial shuttle vector, was randomly modified in vitro using N-acetoxy-N-2-acetylaminofluorene (N-AcO-AAF) as a model reactive metabolite of the carcinogen AAF. The binding spectrum of AAF to the URA3 gene was determined and found to be essentially random, as all guanine residues reacted about equally well with N-AcO-AAF. Independent Ura^– mutants were selected in vivo after transformation of the modified plasmid into a ura3 yeast strain. Plasmid survival decreased as a function of AAF modification, leading to one lethal hit (37% relative survival) for an average of 50 AAF adducts per plasmid molecule. At this level of modification the mutation frequency was equal to 70 × 10^–4, i.e. 50-fold above the background mutation frequency. UV irradiation of the yeast cells did not further stimulate the mutagenic response, indicating the lack of an SOS-like mutagenic response in yeast. Sequence analysis of the URA3 mutants revealed 48% frameshifts, 44% base substitutions and 8 % complex events. While most base substitutions (74%) were found to be targeted at G residues where AAF is known to form covalent C8 adducts, frameshift mutations were observed at GC base pairs in only 24% of cases. Indeed, more than 60% of frameshift events occurred at sequences such as 5-(A/T)_nG-3 where a short (n = 2 or 3) monotonous run of As or Ts is located on the 5' side of a guanine residue. We refer to these mutations as semi-targeted events and present a potential mechanism that explains their occurrence.     

Chromosomal polymorphisms involving telomere fusion,centromeric inactivation and centromere shift in the ant Myrmecia (pilosula) n=1

Detailed karyological surveys of the ant Myrmecia pilosula species group, which is characterized by the lowest chromosome number in higher organisms (2n=2), were attempted. We revealed that this species has developed highly complicated chromosomal polymorphisms. Their chromosome numbers are in the range 2n=2, 3, and 4, and six polymorphic chromosomes are involved, i.e., two for chromosome 1 (denoted as SM₁ and ST₁), three for chromosome 2 (A₂, A₂, and M₂), and M₍₁₊₂₎ for the 2n=2 karyotype. We suggested that these chromosomes were induced from a pseudo-acrocentric (A ₁ ^M ) and A₂ as follows: (1) A ₁ ^M SM₁ or ST₁ by two independent pericentric inversions; (2) A₂A₂M₂ by chromosomal gap insertion and centromere shift; and (3) ST₁+A₂M₍₁₊₂₎ by telomere fusion, where (3) means that the 2n=2 karyotype was derived secondarily from a 2n=4 karyotype. It is a noteworthy finding that active nucleolus organizer (NOR) sites, in terms of silver staining, are tightly linked with the centromere in this species, and that both the centromere and NOR of A₂ were inactivated after the telomere fusion.     

A clinicopathological evaluation of anti-fucosylated antigens antibody (YB-2) in colorectal carcinoma

A newly generated monoclonal antibody, YB-2, reacts simultaneously with Y (Fuc12Gal14[Fuc13]GlcNAc), Le^b (fuc12Gal13[Fuc14]GlcNAc) and H type 2 (Fuc12Gal14GlcNAc) antigens (Jpn J Cancer Res 1993: 84; 641-8). Since these antigens have been reported to be expressed strongly in malignant colorectal tissues, we investigated the usefulness of this antibody as an immunochemical tool for diagnosis of colorectal cancer. The rate of positive staining with YB-2 antibody in colorectal carcinoma (n=101), adenoma (n=26) and normal tissues (n=25) was 95.0, 50.0 and 12.0%, respectively. The specimens with negative staining were restricted in Dukes' A patients but 75% of Dukes' C patients were strongly positive. The intensity of positive staining with YB-2 antibody was also significantly related to the clinico-pathological features such as the depth of invasion, metastasis, histological types and tumor location. Moreover, the 5-year survival in patients whose tumors were positive with YB-2 antibody was found to be significantly low. Therefore, YB-2 antibody could be useful for immunodiagnosis and, possibly, immunotherapy of colorectal carcinoma.     

Testing the “ecologically noble savage” hypothesis: Interspecific prey choice by Piro hunters of Amazonian Peru

Native peoples have often been portrayed as natural conservationists, living in harmony with their environment. It is argued that this perspective is a result of an imprecise definition of conservation that emphasizes effects rather than actual behavior. Using foraging theory as a contrast, an operational definition of conservation is offered. Foraging theory assumes that foragers will behave to maximize their short-term harvesting rate. Hunting decisions that are costly in terms of short-term harvest rate maximization, yet increase the sustainability of the harvest are deemed conservation. Using this definition, alternative hypotheses are tested using data on the inter-specific prey choice decisions of a group of subsistence hunters, the Piro of Amazonian Peru. Results indicate that hunters do not show any restraint from harvesting species identified as vulnerable to over-hunting and local extinction. Decisions are made that are consistent with predictions of foraging theory. The phrase ecologically noble savage was coined by Kent Redford (1991) in a thought provoking article of the same name.     

A continuous migration model with stable demography

A probability model of a population undergoing migration, mutation, and mating in a geographic continuum R is constructed, and an integrodifferential equation is derived for the probability of genetic identity. The equation is solved in one case, and asymptotic analysis done in others. Individuals at x, y R in the model mate with probability V(x, y) dt in any time interval (t, t + dt). In two dimensions, if V(x,y) = V(x–y) where V(x) V(x/)/ ² approaches a delta function, the equilibrium probability of identity vanishes as 0. The asymptotic rate at which this occurs is discussed for mutation rates u u _o > 0 and for Cu , > 0, and u 0.Partially supported by NSF grant MCS79-03472Research was partially supported by Task Agreement No. DE-AT06-76EV71005 under Contract No. DE-AM06-76RL02225 between the U.S. Dept. Energy and the University of Washington     

Natural-killer-stimulatory effect of combined low-dose interleukin-2 and interferon β in hairy-cell leukemia patients

The association of low doses of interleukin-2 (IL-2; 5 IU/ml) and interferon (IFN; 10 IU/ml) induced an additive or synergic stimulatory effect on natural killer (NK) activity (32%) in peripheral blood samples from hairy-cell leukemia patients, both those with active disease and those in remission. The synergic NK stimulatory effect was more commonly found in samples from patients with active disease, while the additive effect was more frequent in the patients in remission. The IL-2/IFN combination provoked a nonadditive nonsynergic NK-stimulatory effect in a further 19.8% samples. The targets of the IL-2/IFN combination were typical NK cells, as shown by the fact that there was increased cytotoxicity (synergic, additive or nonadditive nonsynergic) against the K562, but not the Daudi cell line in peripheral blood mononuclear cell samples treated with the combination of the two cytokines. When CD16⁺/CD56⁺ or CD57⁺/CD16⁺/CD56⁺ cells were removed, the NK-stimulatory effect was lost. The fact that the NK-cell-enhancing activity of the IL-2/IFN combination was reduced when Percoll fractions 2 and 3 were used, but still persisted in 66% of tests, may have been due to cytotoxicity being higher in the untreated fractions 2 and 3 than in the untreated unfractionated samples. One of the factors responsible for the NK-stimulatory effect appears to be the capacity of the IL-2/IFN combination to trigger an increase in IFN synthesis. If similar experiments give like results in samples from patients suffering from other B-cell lymphoproliferative, or HIV-associated disorders, all of which are characterized by a deficiency in NK activity, it should be possible to use low-dose IL-2/IFN to treat these disorders and, perhaps, residual neoplastic disease without exposing the patient to undue toxicity. Further, by testing other combinations one should be able to identify the lowest IL-2 and IFN doses that would effectively boost the additive or synergic effect in a greater number of cases.     

Crassulacean acid metabolism in tropical dicotyledonous trees of the genusClusia

Summary The performance of crassulacean acid metabolism (CAM) by dicotyledonous trees of the genusClusia sampled at three sites in the state of Falcon in northern Venezuela is characterized.Clusia leaves have a somewhat succulent appearance. Unlike leaves of many other CAM plants, which are uniformly built up of very large isodiametric cells, there are distinct layers of palisade and spongy mesophyll, with individual cells being smaller. There is no specialized water storage tissue. ¹³C values indicate thatC. multiflora in the elfin-cloud forest on top of Cerro Santa Ana, at 800 m altitude, performs C₃ photosynthesis (¹³ –27.1). However,C. rosea in the tall cloud forest on Cerro Santa Ana (600m altitude), andC. rosea andC. alata in the dry forest on Serrania San Luis (900 m altitude) perform CAM (¹³C –14.1 to –19.2). InC. alta andC. rosea there were large day-night changes in the levels of malic and citric acids ranging from 63 to 240 mmol 1^–1 for malid acid and from 35 to 112 mmol 1^–1 for citric acid. The sum of the changes in malate and citrate levels accounts for the changes of titratable protons measured. With a day-night change of titratable protons of 768 mmol 1^–1 in one of the analyses,C. rosea showed the highest value yet encountered in a CAM plant. Oscillations of free sugars (fructose, glucose, sucrose) and of starch were also analysed in the CAM performingClusia species. Carbon skeletons of the precursors involved in nocturnal malate and citrate synthesis largely derive from free sugars and not from polyglucan. Unlike some other CAM plants, there is no clear and quantitative correlation between day-night changes of organic acid levels and cell sap osmolality.Dedicated to Professor Dr. Otto L. Lange on the occasion of his 60th birthday.     

Inactivation of voltage-dependent calcium current in an insulinoma cell line

We have studied the mechanism of Ca current inactivation in the -cell line HIT-T15 by conventional and perforated patch recording techniques, using two pulse voltage protocols and a combination of current and tail current measurements. In 5 mM Ca, from a holding potential of - 80 mV, the maximum current showed a complex time course of inactivation: a relatively fast, double exponential inactivation (_h1 12 ms and _h2 60 ms) and a very slowly inactivating component ( > 1 s). The faster component (_h1) was due to the voltage-dependent inactivation of a low-threshold-activated (LVA), T-type current, which deactivates more slowly ( 3–5 ms) than the other components ( 0.2–0.3 ms). The intermediate component (_h2) was due to the Ca-dependent inactivation of a portion of the high-threshold-activated (HVA) current. A saturating dose of the dihydropyridine (DHP) nifedipine (10 M) did not affect the LVA current, but inhibited by 68 ± 5% the transient, Ca-sensitive portion of the HVA current and by 33 ± 12% the long lasting component. We suggest that three components of the calcium current can be resolved in HIT cells and the main target of DHPs is a HVA current, which inactivates faster than the DHP-resistant HVA component and does so primarily through calcium influx. Correspondence to: C. Marchetti     

Second-derivative Fourier transform infrared spectra of seaweed galactans

The Fourier transform infrared spectra of agar, agarose, -, -, and -carrageenan, and ofChondrus canaliculatus, Iridaea ciliata, I. membranacea, I. laminarioides andGracilaria chilensis polysaccharides were recorded in the 4000–400 cm^-1 region. The bands in the second derivative mode are sharper and more bands are resolved than in the normal spectra.Agar, agarose andG. chilensis phycocolloids exhibit diagnostic bands at 790 and 713 cm^-1. -, - and -carrageenans, and native carrageenan-type polysaccharides fromC. canaliculatus andIridaea species exhibit bands at around 1160, 1140, 1100, 1070, 1040, 1008, 610, and 580 cm^-1. Therefore, FT-IR spectroscopy in the second-derivative mode may be applied to differentiate between agar- and carrageenan-types seaweed galactans.