Immunocytochemical localization of lysozyme and surfactant protein A in rat type II cells and extracellular surfactant forms.

Using immunogold labeling of fixed, cryosubstituted tissue sections, we compared the distribution of lysozyme, an oxidant-sensitive lamellar body protein, with that of surfactant protein A (SP-A) in rat Type II cells, extracellular surfactant forms, and alveolar macrophages. Morphometric analysis of gold particle distribution revealed that lysozyme and SP-A were present throughout the secretory and endosomal pathways of Type II cells, with prominent localization of lysozyme in the peripheral compartment of lamellar bodies. All extracellular surfactant forms were labeled for both proteins with preferential labeling of tubular myelin and unilamellar vesicles. Labeling of tubular myelin for SP-A was striking when compared with that of lamellar bodies and other extracellular surfactant forms. Lamellar body-like forms and multilamellar structures were uniformly labeled for lysozyme, suggesting that this protein is rapidly redistributed within these forms after secretion of lysozyme-laden lamellar bodies. By contrast, increased labeling for SP-A was observed over peripheral membranes of lamellar body-like forms and multilamellar structures, apparently reflecting progressive SP-A enrichment of these membranes during tubular myelin formation. The results indicate that lysozyme is an integral component of the lamellar body peripheral compartment and secreted surfactant membranes, and support the concept that lysozyme may participate in the structural organization of lung surfactant.     

Cyclophosphamide and abrogation of tumor-induced suppressor T cell activity

Summary Previously we have demonstrated that the in vitro generation of P815-specific anti-tumor cytotoxic T lymphocytes (CTL) was suppressed by splenic suppressor T cells from late tumor-bearing hosts (TBH). Suppression is not caused by in vitro growth of P815 from splenic metastases, since suppression was also seen with spleen cells from late TBH mice bearing a hypoxanthine/aminopterin/thymidine-sensitive subline (PHS-5) of P815 in the presence of HAT. Cyclophosphamide has been shown to inhibit theinduction of suppressor cells selectively in a number of immune responses, but evidence that it can inhibit active tumor-induced suppressor T cells is limited. We have found that suppressor T cells already induced by P815 in syngeneic late TBH are sensitive to low doses of cyclophosphamide (50 mg/kg) given 1 day before spleen harvest, but the in vitro CTL response of late TBH spleen cells could not be restored by pretreating the mice with cyclophosphamide, even when exogenous interleukin-2 was added to the cultures. Although 50 mg/kg cyclophosphamide did not inhibit the CTL response of spleen cells from mice immunized with P815 +Corynebacterium parvum, the same dose of cyclophosphamide eliminated the CTL response of spleen cells from early TBH. Interleukin-2 (IL-2) did not overcome this effect of cyclophosphamide, suggesting a direct effect on CTL. Ultra-low-dose cyclophosphamide (10 mg/kg) did not adversely effect early TBH CTL but was still able to eliminate suppressor T cell activity from late TBH. Nevertheless, late TBH CTL remained unresponsive after pretreatment of mice with ultra-low-dose cyclophosphamide, even when exogenous IL-2 was added in vitro. CTL precursor frequency analyses demonstrated that cyclophosphamide pretreatment had little or no effect on the numbers of CTL precursors from early TBH. Late TBH CTL precursor cells were not detectable in these studies, with or without suppressor T cell inhibition by cyclophosphamide pretreatment. Thus, it appears that most CTL precursor cells may be lost or irretrievably inactivated in the spleens of late TBH mice.This work was supported by grants CA42443, CA48075 and T32-CA09210 from the National Cancer Institute, Department of Health and Human Services, and an American Cancer Society Clinical Oncology Career Development Award (H. D. Bear)     

Segmental specialization of neuronal connectivity in the leech

1. Every segmental ganglion of the leech Hirudo medicinalis contains two serotonergic Retzius cells. However, Retzius cells in the two segmental ganglia associated with reproductive function are morphologically distinct from Retzius cells elsewhere. This suggested that these Retzius cells might be physiologically distinct as well. 2. The degree of electrical coupling between Retzius cells distinguishes the reproductive Retzius cells; all Retzius cells are coupled in a non-rectifying manner, but reproductive Retzius cells are less strongly coupled. 3. Retzius cells in standard ganglia depolarize following swim motor pattern initiation or mechanosensory stimulation while Retzius cells in reproductive ganglia either do not respond or hyperpolarize. 4. In standard Retzius cells the depolarizing response caused by pressure mechanosensory neurons has fixed latency and one-to-one correspondence between the mechanosensory neuron action potentials and Retzius cell EPSPs. However, the latency is longer than for most known monosynaptic connections in the leech. 5. Raising the concentration of divalent cations in the bathing solution to increase thresholds abolishes the mechanosensory neuron-evoked EPSP in standard Retzius cells. This suggests that generation of action potentials in an interneuron is required for production of the EPSP, and therefore that the pathway from mechanosensory neuron to Retzius cell is polysynaptic. 6. P cells in reproductive segments have opposite effects on reproductive Retzius cells and standard Retzius cells in adjacent ganglia. Thus the difference in the pathway from P to Retzius is not localized specifically in the P cell, but elsewhere in the pathway, possibly in the type of receptor expressed by the Retzius cells.     

Avian model for 13-cis-retinoic acid embryopathy: demonstration of neural crest related defects

The effects of 13-cis-retinoic acid on the developing chick embryo were investigated. Fertilized eggs were injected via the yolk sac with single 50 microliters doses of either 1.5 micrograms, 15 micrograms, or 150 micrograms of 13-cis-retinoic acid in dimethyl sulfoxide on varying days of incubation (embryonic days 2, 3, 4, 5, or 6). Control embryos were given solvent alone or a mock injection. The embryos were examined on day 14 of incubation. The effects of retinoic acid on mortality and total malformations were both dose and developmental-stage responsive. The defects caused by 13-cis-retinoic acid occurred in mesenchymal tissues derived in part from the cranial neural crest ectomesenchyme. The craniofacial and cardiovascular malformations produced in the chick are analogous to those seen in animal models of retinoid teratogenesis and in human fetuses exposed to 13-cis-retinoic acid during maternal therapy for cystic acne. Following 13-cis-retinoic acid treatment, craniofacial and specific cardiovascular malformations were increased significantly compared to those in matched solvent and mock treated controls. The greatest number of malformations occurred when 13-cis-retinoic acid was given after cranial neural crest cell migration was complete. We propose that the primary effect of 13-cis-retinoic acid is on region-specific localization and differentiation of the mesenchymal subpopulation of cranial neural crest cells.     

Increase in ovarian kallikrein activity during ovulation in the gonadotrophin-primed immature rat

The ovulatory process was initiated in 25-day-old rats by injecting them with hCG (10 i.u., s.c.) 2 days after the animals had been primed with PMSG (10 i.u., s.c.). At 2-h intervals after hCG, the ovaries were extracted and assayed for glandular kallikrein activity by using a chromogenic substrate (H-D-Val-Leu-Arg-p-nitroanilide) which exhibits optical density (at 405 nm) upon hydrolysis. In 0-h control ovaries the activity was 12.5 x 10(-3) kallikrein units (KU)/mg protein and it increased to a peak of 56.6 x 10(-3) KU/mg at 12 h after hCG, when the follicles first began to rupture. The kallikrein activity was distinguishable from ovarian plasminogen activator activity on the basis of pH optima and response to trypsin inhibitor (SBTI). The activity was inhibited by a s.c. dose of indomethacin of 0.3 mg/rat, or higher, and this dosage inhibited ovulation. The results suggest that kallikrein activity contributes to the degradation of Graafian follicles during ovulation in mammals.     

OsPIN2, which encodes a member of the auxin efflux carrier proteins,is involved in root elongation growth and lateral root formation patterns via the regulation of auxin distribution in rice

Auxin flow is important for different root developmental processes such as root formation, emergence, elongation and gravitropism. However, the detailed information about the mechanisms regulating the auxin flow is less well understood in rice. We characterized the auxin transport‐related mutants, Ospin‐formed2‐1 (Ospin2‐1) and Ospin2‐2, which exhibited curly root phenotypes and altered lateral root formation patterns in rice. The OsPIN2 gene encodes a member of the auxin efflux carrier proteins that possibly regulates the basipetal auxin flow from the root tip toward the root elongation zone. According to DR5‐driven GUS expression, there is an asymmetric auxin distribution in the mutants that corresponded with the asymmetric cell elongation pattern in the mutant root tip. Auxin transport inhibitor, N‐1‐naphthylphthalamic acid and Ospin2‐1 Osiaa13 double mutant rescued the curly root phenotype indicating that this phenotype results from a defect in proper auxin distribution. The typical curly root phenotype was not observed when Ospin2‐1 was grown in distilled water as an alternative to tap water, although higher auxin levels were found at the root tip region of the mutant than that of the wild‐type. Therefore, the lateral root formation zone in the mutant was shifted basipetally compared with the wild‐type. These results reflect that an altered auxin flow in the root tip region is responsible for root elongation growth and lateral root formation patterns in rice.     

Local context and connectivity determine the response of zooplankton communities to salt contamination

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Target-detection by the echolocating bat,Eptesicus fuscus

Summary The long-range echo-detection capabilities of echolocating bats (Eptesicus fuscus) were studied in a two-choice psychophysical procedure.E. fuscus can detect 4.8 mm diameter spheres at a distance of 2.9 m, and 19.1 mm diameter spheres at a distance of 5.1 m. The threshold of echo-detection corresponds to the distance at which a target returns an echo amplitude in the region of 0 dB SPL. The results demonstrate that the maximum effective range of bat sonar is greater than previously indicated by obstacleavoidance and target-interception tasks.     

The effect of humidity on growth and feed conversion of broiler chickens

The optimum range of relative humidity for chicken after brooding is between 50 and 70%. The range is between 60% and 80% relative humidity during the brooding period. The higher humidities seem to favor better growth and feed conversion. However, one must be careful since the higher humidities seem to favor problems with wet litter, housing and some diseases. Dehydration did not occur under conditions of these tests. Feed conversion, feathering,pigmentation and gain of the chicken is aversely affected by high relative humidities above 26.7°C temperature. Chicken raised at 35° to 37.8°C regardless of humidity do not perform satisfactorily. The importance of water cannot be overlooked as was shown in these trials.The chicken requires approximately 0.68 kg of water per kg of feed consumed and almost 1.59 kg of water for each kg of gain. If the water is unpalatable, contaminated or high in mineral salts consumption can be reduced thus causing a reduction in growth and efficiency.

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Zusammenfassung Der optimale Bereich der Relativen Feuchte für Hühner nach dem Brüten liegt zwischen 50 und 70%, der Bereich während der Brutperiode zwischen 60 und 80%. Höhere Feuchten scheinen ein besseres Wachstum und eine bessere Nahrungsverwertung zu begünstigen. Jedoch muss man vorsichtig sein, weil die höheren Feuchten Schwierigkeiten wie feuchte Streu und Behausung sowie einige Krankheiten begünstigen. Austrocknung kam unter diesen Versuchsbedingungen nicht vor. Futterverwertung, Gefieder, Pigmentierung und Gewichtszunahme werden durch hohe Relative Feuchten bei Temperaturen über 26,7°C ungünstig beeinflusst. Hühner, die bei 35 bis 37,8°C ohne Rücksicht auf die Relative Feuchte gezüchtet wurden,befriedigten nicht. Die Bedeutung des Wassers darf nicht übersehen werden. Das Huhn benötigt annähernd 0,68 kg Wasser je Kg Futterverbrauch und fast 1,59 kg Wasser für jedes kg Gewichtszunahme. Wenn das Wasser nicht schmackhaft oder verunreinigt ist oder einen hohen Gehalt von Mineralsalzen besitzt, kann der Verbrauch reduziert und so eine Beeinträchtigung des Wachstums und der Leistungsfähigkeit verursacht werden.

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Resume L'humidité optimum pour le développement des poulets fraîchement éclos est située entre 50 et 70%. Durant la couvaison, cet optiumum se situe entre 60 et 80%. Une humidité plus élevée semble favoriser la croissance et une meilleure mise en valeur de la nourriture. Il faut pourtant être prudent dans le réglage de l'humidité, car, si elle est trop élevée, elle semble favoriser certaines maladies et apporte des difficultés d'élevage dues au poulailler lui-même et au fait que la litière est humide. On n'as pas constaté de phénomènes de déshydratation au cours de ces essais. Au-dessus de 26,7°C, une forte humidité influence de façon défavorable la nutrition, le plumage, la pigmentation et le développement des poulets. Des poulets élevés entre 35° et 37,8°C sans qu'on tienne compte de l'humidité ne donnent pas satisfaction. Dans les présents essais, on a également mis en évidence l'importance de l'eau. Les poulets ont besoin d'environ 0,68 kg d'eau par kg de nourriture et d'à peu près 1,59 kg d'eau par kg de poids. Si l'eau a un goût désagréable, si elle est polluée ou si elle présente une forte teneur en sels minéraux, les poulets en boivent moins et leur développement en est diminué d'autant.

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Presented at the Fourth International Biometeorological Congress, New Brunswick, N.J., 26 August–2 September 1966. Scientific Article Number A-1291. Contribution No. 3832 of the Maryland Agricultural Experiment Station.