Nuclear volume and number in long-term in vitro cultures of Puccinia graminis

1982 ◽  
Vol 60 (9) ◽  
pp. 1827-1836 ◽  
Author(s):  
W. R. Bushnell ◽  
Patricia L. Bosacker

Eight cultures of Puccinia graminis f. sp. tritici which had been serially subcultured in the Cereal Rust Laboratory for 2–13 years were examined for nuclear volume, number of nuclei per cell, and dimensions of hyphae. The cultures were of two types: compact with short, wide hyphal cells (ca. 10 × 22 μm); and fluffy with long, narrow cells (ca. 5 × 80 μm). The compact cultures tended to sporulate; the fluffy ones did not. By using volume of hyphal nuclei to estimate ploidy, the cultures were judged to be of three types: compact with two haploid nuclei per cell; compact with one diploid nucleus per cell; and fluffy with two diploid nuclei per cell. The compact cultures originated from American uredial isolates of races 17, 23, 38, and 56. The fluffy cultures originated only from University of Sydney uredial isolate 334, race 126Anz6,7, or as variants of compact cultures from American race 56. A uninucleate fluffy culture which had been initiated from uredial isolate 334 by Australian workers had a nuclear volume four times those of binucleate compact cultures, suggesting that the nucleus of each cell was tetraploid. A culture of P. graminis f. sp. secalis initiated at the Cereal Rust Laboratory was compact and had mostly four nuclei per cell, each presumed to be haploid. Generally, compact cultures had more characteristics in common with the parasitic form of P. graminis than fluffy cultures did.

2015 ◽  
Vol 39 ◽  
pp. S35
Author(s):  
C. Ichim ◽  
D. Koos ◽  
T. Ichim ◽  
R. Wells
Keyword(s):  

2012 ◽  
Vol 68 (3) ◽  
pp. 533-538 ◽  
Author(s):  
Wellington Ronildo Clarindo ◽  
Carlos Roberto Carvalho ◽  
Maria Andréia Corrêa Mendonça

1978 ◽  
Vol 148 (3) ◽  
pp. 823-828 ◽  
Author(s):  
J W Schrader ◽  
S Schrader

In vitro cultures of mouse bone marrow cells, maintained for periods up to 7 wk, were shown to contain cells able to repopulate irradiated hosts with T and B lymphocytes. The lymphocytes were fully functional and there did not appear to be any gross restriction of their receptor repertoire. The cultured cells reconstituted irradiated semiallogenic hosts without evidence of graft-versus-host disease, suggesting that culture of donor marrow might be a useful preliminary to transplantation when tissue matching is incomplete.


2020 ◽  
Vol 11 ◽  
Author(s):  
Gabriela Torres-Silva ◽  
Elyabe Monteiro Matos ◽  
Ludmila Freitas Correia ◽  
Evandro Alexandre Fortini ◽  
Wellington Santos Soares ◽  
...  

2018 ◽  
Vol 24 (4) ◽  
pp. 211-220 ◽  
Author(s):  
C L Depoix ◽  
F Haegeman ◽  
F Debiève ◽  
C Hubinont
Keyword(s):  

2011 ◽  
Vol 76 (3) ◽  
pp. 193-199 ◽  
Author(s):  
Katarzyna Goller ◽  
Jan J. Rybczyński

Experiments had been carried out on gametophytes and very young fronds of sporophytes with application of Murashige and Skoog (1962) medium. The paper described the results of 15 years in vitro experiments on 16 species of tree ferns belonging to various genera: <em>Blechnum</em>, <em>Cibotium</em>, <em>Cyathea</em> and <em>Dicksonia</em>. Genus <em>Cyathea</em> was represented by: <em>C. australis</em> (R.Br.) Domin., <em>C. capensis</em> (L.f.) Sm., <em>C. cooperi</em> (F.Muell.) Domin, <em>C. brownii</em> Domin, <em>C. dealbata</em> (G.Forest) Sw., <em>C. dregei</em> Kunze, <em>C. leichhardtiana</em> (F.Muell.) Copel., <em>C. robertsiana</em> (F.Muell.) Domin., <em>C. schanschin</em> Mart., <em>C. smithii</em> Hook.f. and <em>Cyathea</em> sp. In case of genus <em>Dicksonia</em> only two species were introduced into our experiments: <em>D. fibrosa</em> Colenso and <em>D. sellowiana</em> Hook.. Taxa <em>Blechnum</em> was presented by <em>B. brasiliense</em> Desv. and <em>Cibotium</em> by <em>C. glaucum</em> (Sm.) Hook. and Arn. and <em>C. schiedei</em> Schltdl. and Cham.. The studied species presented various responses on culture conditions depending on the level of stage of development. Time required for spores germination differed between species and took from only a few to 16 weeks. Prothalium formations showed various types of growth presented by marginal meristems. For all investigated species long term gametophyte in vitro cultures was established. Mature gametophyte possessed functional antheridia and archegonia. Spontaneous fertilization helped to establish the culture of young sporophytes. For all species the ex vitro culture in greenhouse collection was established. Manipulation of sucrose content in the medium stimulated the multiplication of gametophytes, but its lack induced formation of gemmae. Apospory was observed when culture of very young fronds was extended for 6 months and new generation of gametophytes was developed. Finally, sporophytes of 12 species were obtained and they have been growing in our greenhouse.


2021 ◽  
Vol 23 (Supplement_6) ◽  
pp. vi25-vi25
Author(s):  
Simranjit Singh ◽  
Landon Hansen ◽  
Changzheng Du ◽  
Kristen Roso ◽  
Rui Yang ◽  
...  

Abstract Glioblastoma (GBM) is a lethal brain cancer that exhibits high levels of drug resistance, a feature partially imparted by tumor cell stemness. Recent work has shown that homozygous MTAP deletion, a frequent genetic alteration in GBM, promotes the stemness of GBM cells. Here, exploiting the MTAP loss-conferred deficiency in adenine salvage, we demonstrated that subtle levels of adenine blockade via treatment with Alanosine, an inhibitor of de novo adenine synthesis, attenuate the stemness of MTAP-null GBM cells. Transcriptomic profiling performed on Alanosine-treated GBM cells revealed a reduction of mitochondrial DNA-encoded gene expression. Furthermore, Seahorse XF analysis showed that Alanosine treatment led to a reduction in mitochondrial respiration and eliminated GBM cells’ spare respiratory capacity, an important metabolic measure of cell fitness that is representative of their ability to respond to oxidative stress. Importantly, long term adenine shortage via treatment with low doses of Alanosine resulted in similarly compromised mitochondria functionality and attenuated GBM cells’ stemness. In further supporting this adenine blockade – compromised mitochondria – reduced stemness cascade, treatment with a mitochondrial respiration inhibitor attenuated the stemness of GBM cells, suggesting the importance of mitochondrial function in maintaining GBM stemness. Finally, in agreement with the diminished stemness and compromised mitochondrial function, we showed that Alanosine sensitized GBM cells to temozolomide (TMZ) in both in vitro cultures and in an orthotopic GBM model. Collectively, these results identify critical roles of adenine supply in maintaining stemness and mitochondrial function in GBM cells, suggest a targeted method of abrogating stemness and chemoresistance in GBMs, and support targeting adenine synthesis as a complementary approach for treating the half of GBMs harboring MTAP deletions.


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