Elektronenmikroskopische Untersuchungen am Interstitiellen Gewebe des Rattenhodens,unter Besonderer Berücksichtigung der Leydigschen Zwischenzellen

Zusammenfassung Die elektronenmikroskopische Untersuchung des Interstitiums des Rattenhodens nach Fixierung mit Glutaraldehyd und Nachfixierung mit Osmiumtetroxyd bestätigte das Vorkommen von dunklen und hellen Leydig-Zellen.Die dunkle Leydig-Zelle besitzt ein tubular gestaltetes, feinmaschiges, dicht gepacktes agranuläres endoplasmatisches Reticulum. Sie ist reicher an einzelnen und an rosettenförmig gelagerten Ribosomen als die helle Zelle. Sie ist mit einem typischen Ergastoplasma, somit mit einem Proteinsyntheseapparat ausgestattet. Der Golgi-Apparat ist geringer entfaltet, die Mitochondrien sind dichter und kleiner als in hellen Zellen. Ferner zeichnet sich die dunkle Zelle durch das Vorkommen von Glykogengranula aus.In der hellen Leydig-Zelle wird die Cytoplasmastruktur von dem bläschenförmig gestalteten agranulären endoplasmatischen Reticulum beherrscht. Tubuli sind in einzelnen Zellen und Zellbezirken zwar nachweisbar, stehen aber im Verhältnis zu den Bläschen ganz im Hintergrund. Typisches Ergastoplasma fehlt. Die Mitochondrien sind hell und groß sowie arm an Binnenstrukturen. Der Golgi-Apparat ist durch besonders große Golgi-Vakuolen gekennzeichnet. Glykogen fehlt.Außer den Leydig-Zellen wird die Ultrastruktur der Tubuluswand, insbesondere der sog. kontraktilen Zellen und der neben den Leydig-Zellen im Interstitium vorhandenen Fibrocyten, Histiocyten und Lymphocytenc?) beschrieben.

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Summary The electron microscopic investigation of the interstitium of rat testis after fixation in glutaraldehyde and subsequent fixation with osmiumtetroxyde confirmed the existence of dark and clear Leydig-cells.The dark Leydig-cells possess a tubule-formed, fine-meshed, tightly packed, agranular, endoplasmatic reticulum. They have more ribosomes — single or arranged in rosettes — than the clear cells. They have a typical ergastoplasm, i.e. an apparatus for protein-synthesis. The Golgi-apparatus is less developed, the mitochondria are denser and smaller than in the clear cells. Furthermore the presence of glycogen granules is characteristic for the dark cell-type.In the clear cells a vesicle-shaped, agranular, endoplasmic reticulum is predominant. In some cells and regions of cells tubules are detectable but in comparison to the vesicles they are rare. Typical ergastoplasm is lacking. The mitochondria are clear, voluminous and the inner structures are poorly developed. The Golgi-apparatus is characterized by especially large Golgi-vacuoles. Glycogen is missing.Besides the Leydig-cells the ultrastructure of the tubular elements especially of the socalled contractile cells as well as the structure of the fibrocytes, histiocytes and lymphocytes (?), located in the interstitium, is described.

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Mit Unterstützung durch die Deutsche Forschungsgemeinschaft.

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Forschungsstipendiat der Alexander von Humboldt-Stiftung 1964–1965.     

Comparison of the mating behaviour between two sympatric species,Nezara antennata andN. viridula (Heteroptera: Pentatomidae), with special reference to sound emission

Mating behaviour and associated songs were compared between 2 sympatric congeneric species,Nezara antennata andN. viridula, between which interspecific mating was known to occur under natural conditions. The fundamental sequence of mating behaviour for these species was the same. Three kinds of songs were recorded from each sex ofN. antennata. ForN. viridula, 4 kinds of male songs and 3 kinds of female songs were recorded. The songs which corresponded with definite behavioural bouts were distinct between these species. Some consideration was made as to why interspecific differences in the songs did not sufficiently engender ethological isolation. In addition, some geographic variations in the songs were shown among Yugoslavian (Čokl et al. 1972), American (Harris et al. 1982) and Japanese populations ofN. viridula. These variations were relatively inconspicuous when compared with the interspecific differences fromN. antennata.     

Conversion of gibberellin A20 to gibberellins A1 and A5 in a cell-free system from Phaseolus vulgaris

The soluble fraction of a cell-free system from immature seeds of Phaseolus vulgaris L. converts gibberellin A₂₀ (GA₂₀) to GA₁ and GA₅. It does however not metabolize GA₁ and GA₂₉ to GA₅, showing that in this system GA₂₀ is converted directly to GA₅. The steps from GA₂₀ to GA₁ (3-hydroxylation) and from GA₂₀ to GA₅ (² double-bond formation) require oxygen, Fe²⁺ and -ketoglutarate, and are stimulated by ascorbate. The enzymes catalyzing these conversions bate. The enzymes catalyzing these conversions have properties similar to those of GA oxidases found in Cucurbita maxima and Pisum sativum.Abbreviations GA_n gibberellin A_n - HPLC high-performance liquid chromatography - GC-MS combined gas chromatography-mass spectrometry - TLC thin-layer chromatography - TMSi/TMSi trimethylsilyl ether/trimethylsilyl ester Graduate student, University of Tokyo     

Detecting latitudinal and altitudinal expansion of invasive bamboo Phyllostachys edulis and Phyllostachys bambusoides (Poaceae) in Japan to project potential habitats under 1.5°C–4.0°C global warming

Rapid expansion of exotic bamboos has lowered species diversity in Japan's ecosystems by hampering native plant growth. The invasive potential of bamboo, facilitated by global warming, may also affect other countries with developing bamboo industries. We examined past (1975–1980) and recent (2012) distributions of major exotic bamboos (Phyllostachys edulis and P. bambusoides) in areas adjacent to 145 weather stations in central and northern Japan. Bamboo stands have been established at 17 sites along the latitudinal and altitudinal distributional limit during the last three decades. Ecological niche modeling indicated that temperature had a strong influence on bamboo distribution. Using mean annual temperature and sun radiation data, we reproduced bamboo distribution (accuracy = 0.93 and AUC (area under the receiver operating characteristic curve) = 0.92). These results infer that exotic bamboo distribution has shifted northward and upslope, in association with recent climate warming. Then, we simulated future climate data and projected the climate change impact on the potential habitat distribution of invasive bamboos under different temperature increases (i.e., 1.5°C, 2.0°C, 3.0°C, and 4.0°C) relative to the preindustrial period. Potential habitats in central and northern Japan were estimated to increase from 35% under the current climate (1980–2000) to 46%–48%, 51%–54%, 61%–67%, and 77%–83% under 1.5°C, 2.0°C, 3.0°C, and 4.0°C warming levels, respectively. These infer that the risk areas can increase by 1.3 times even under a 1.5°C scenario and expand by 2.3 times under a 4.0°C scenario. For sustainable ecosystem management, both mitigation and adaptation are necessary: bamboo planting must be carefully monitored in predicted potential habitats, which covers most of Japan.     

Reactivation of Insertionally Inactivated Shiga Toxin 2 Genes of Escherichia coli O157:H7 Caused by Nonreplicative Transposition of the Insertion Sequence

IS1203v is an insertion sequence which has been found in inactivated Shiga toxin 2 genes of Escherichia coli O157:H7. We analyzed the transpositional mechanism of IS1203v in order to investigate whether the Shiga toxin 2 genes inactivated by IS1203v could revert to the wild type. When the transposase activity of IS1203v was enhanced by artificial frameshifting, IS1203v was obviously excised from the Shiga toxin 2 gene in a circular form. The IS1203v circle consisted of the entire IS1203v, but an extra 3-bp sequence (ATC) intervened between the 5′ and 3′ ends of IS1203v. The extra 3-bp sequence was identical to a direct repeat which was probably generated upon insertion. Moreover, we detected the Shiga toxin 2 gene with a precise excision of IS1203v. In the wild-type situation, the transposition products of IS1203v could be observed by PCR amplification. These results show that IS1203v can transpose in a nonreplicative manner and that the Shiga toxin gene inactivated by this insertion sequence can revert to the wild type.     

Biophysical effect of amino acids on the prevention of protein aggregation

Each protein folds into a unique and native structure spontaneously. However, during the unfolding or refolding process, a protein often tends to form aggregates. To establish a method to prevent undesirable protein aggregation and to increase the stability of native protein structures under deterioration conditions, two types of aggregation conditions, thermal unfolding-induced aggregation and dilution-induced aggregation from denatured state, were studied in the presence of additional amino acids and ions using lysozyme as a model protein. Among 15 amino acids tested, arginine exhibited the best results in preventing the formation of aggregates in both cases. Further biophysical studies revealed that arginine did not change the thermal denaturation temperature (T(m)) of the lysozyme. The preventive effect of arginine on aggregation was not dependent on the size or isoelectric point of eight kinds of proteins tested.     

qUVR-10, a major quantitative trait locus for ultraviolet-B resistance in rice, encodes cyclobutane pyrimidine dimer photolyase

Rice qUVR-10, a quantitative trait locus (QTL) for ultraviolet-B (UVB) resistance on chromosome 10, was cloned by map-based strategy. It was detected in backcross inbred lines (BILs) derived from a cross between the japonica variety Nipponbare (UV resistant) and the indica variety Kasalath (UV sensitive). Plants homozygous for the Nipponbare allele at the qUVR-10 locus were more resistant to UVB compared with the Kasalath allele. High-resolution mapping using 1850 F(2) plants enabled us to delimit qUVR-10 to a <27-kb genomic region. We identified a gene encoding the cyclobutane pyrimidine dimer (CPD) photolyase in this region. Activity of CPD photorepair in Nipponbare was higher than that of Kasalath and nearly isogenic with qUVR-10 [NIL(qUVR-10)], suggesting that the CPD photolyase of Kasalath was defective. We introduced a genomic fragment containing the CPD photolyase gene of Nipponbare to NIL(qUVR-10). Transgenic plants showed the same level of resistance as Nipponbare did, indicating that the qUVR-10 encoded the CPD photolyase. Comparison of the qUVR-10 sequence in the Nipponbare and Kasalath alleles revealed one probable candidate for the functional nucleotide polymorphism. It was indicated that single-base substitution in the CPD photolyase gene caused the alteration of activity of CPD photorepair and UVB resistance. Furthermore, we were able to develop a UV-hyperresistant plant by overexpression of the photolyase gene.     

Matrix metalloproteinase-7 degrades all insulin-like growth factor binding proteins and facilitates insulin-like growth factor bioavailability

Proteolytic modification of insulin-like growth factor binding proteins (IGFBPs) plays an important physiological role in regulating insulin-like growth factor (IGF) bioavailability. Recently, we demonstrated that matrix metalloproteinase-7 (MMP-7)/Matrilysin produced by various cancer cells catalyzes the proteolysis of IGFBP-3 in vitro and regulates IGF bioavailability, resulting in an anti-apoptotic effect against anchorage-independent culture. In the present study, we investigated whether MMP-7 contributes to proteolysis of the other five IGFBPs, IGFBP-1, IGFBP-2, IGFBP-4, IGFBP-5, and IGFBP-6, and whether this results in phosphorylation of the IGF type 1 receptor (IGF-1R). MMP-7 cleaved all six IGFBPs, resulting in IGF-mediated IGF-1R phosphorylation, which was inhibited by EDTA treatment. These results suggest that MMP-7 derived from cancer cells can regulate IGF bioavailability in the microenvironment surrounding the tumor, where various kinds of IGF/IGFBP complexes are found, thereby favoring cancer cell growth and survival during the processes of invasion and metastasis.