SHORT-TERM STORAGE OF HUMAN LYMPHOCYTES PRIOR TO IN VITRO STIMULATION1,2

1974 ◽  
Vol 17 (1) ◽  
pp. 37-41 ◽  
Author(s):  
RICHARD J. MANGI ◽  
FRED S. KANTOR
2012 ◽  
Vol 47 (3) ◽  
pp. 344-350 ◽  
Author(s):  
Rafael de Carvalho Silva ◽  
Zanderluce Gomes Luis ◽  
Jonny Everson Scherwinski-Pereira

The objective of this work was to evaluate the large-scale propagation of grapevine genotypes after short-term storage in vitro. Microshoots from ten grapevine genotypes were used. The following storage temperatures were evaluated: 10, 20, and 25°C. After short-term storage, the shoots were propagated in up to five successive subcultures, to assess the large-scale propagation of the germplasm maintained under conditions of minimal growth. The propagated shoots were rooted in different concentrations of indolbutiric acid (IBA) and acclimatized in greenhouse. The best temperature for short-term storage in vitro and survival of the genotypes was 20°C. In the propagation phase, the highest number of shoots per explant was found in the subcultures 4 and 5, with averages of 4.9 and 4.8 shoots per explant, respectively. In the rooting phase, the best results for number of roots were obtained using a culture medium supplemented with 0.4 µmol L-1 of IBA, with an average of three roots per shoot. During the acclimation phase, a survival rate higher than 95% was achieved after 30 days in the greenhouse. Grapevine genotypes maintained for six months in vitro, at 20ºC, can be micropropagated in large scale.


2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
Sreelekshmi R. Nair ◽  
C. S. Geetha ◽  
P. V. Mohanan

Pyrogens are heterogeneous group of fever-inducing substances derived from Gram-positive and Gram-negative bacteria, fungi, and viruses. They incite immune response by producing endogenous pyrogens such as prostaglandins and other proinflammatory cytokines like IL-1β, IL-6, and TNF-α. The present study was to analyze the influence of cryopreservation in IL-1βrelease, a marker for inflammatory response from human lymphocytes, in response to exogenous pyrogenic stimulants. Lymphocytes isolated from pooled blood of multiple healthy individuals were cryopreserved in DMSO and glycerol for periods of 7, 14, 30, and 60 days and were challenged with LPS and LTAin vitro. The inflammatory cytokine, IL-1βrelease, was measured by ELISA method. It was observed that the release of IL-1βincreases instantaneously after the initiation of incubation and reaches a maximum at 3 to 5 hours and then gradually decreases and gets stabilized for both pyrogens. Moreover it was also observed that the effect of cryoprotectants, DMSO (10%) and glycerol (10%), showed almost similar results for short-term storage, but DMSO-preserved lymphocytes yielded a better viability for long-term storage. Thus, the isolated cryopreserved lymphocytes system can be a promising approach for the total replacement/alteration to animal experimentation for pyrogenicity evaluation.


1977 ◽  
Vol 89 (2) ◽  
pp. 511-512 ◽  
Author(s):  
M. J. De Maine

SummaryTwo methods of storing pollen of the dihaploid-inducing Dutch (Wageningen) Solatum phureja clone, IVP 48, are described. Pollination results showed that the functional fertility of one type of stored pollen is similar to that of fresh pollen when used in dihaploid induction crosses on tetraploid potatoes. No obvious relationship was found between the in vitro germination of the pollen samples and their functional fertilities in dihaploid induction crosses.


1998 ◽  
Vol 49 (1) ◽  
pp. 249 ◽  
Author(s):  
M.R. Schneider ◽  
J. Schwartz ◽  
H.-D. Reichenbach ◽  
J.L. Rodrigues

2010 ◽  
Vol 125 (4) ◽  
pp. 761-766 ◽  
Author(s):  
S. Gopala Sundararaj ◽  
Anuradha Agrawal ◽  
Rishi K. Tyagi

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