Nicotiana glauca × Nicotiana langsdorffii tumor hybrid: growth, morphology, polyamines and nucleic acids in vitro

1980 ◽  
Vol 58 (21) ◽  
pp. 2285-2293 ◽  
Author(s):  
D. Serafini Fracassini ◽  
N. Bagni ◽  
P. Torrigiani

Callus of the tumor hybrid of Nicotiana glauca × N. langsdorffii grew better on agar in flasks than on liquid medium in flasks or on agar medium in Petri dishes. Asymmetric callus without roots produced small leaves and parenchyma cells were the most common type of cell. Few meristematic clusters were present, but these were very active during exponential and deceleration growth phases. The volume of their nucleoli, which were large and stained intensely, was used as a marker of the cell cycle. Shortly after transplantation the tissue divided synchronously, but thereafter it became asynchronous. An investigation of nucleic acids and polyamines showed that subcultures initiated a rapid synthesis and accumulation of DNA; thereafter the levels of tRNA and rRNA increased, especially in the deceleration phase, the amount of tRNA always being higher than rRNA. The polyamines putrescine and spermidine are always in larger amounts than in the normal tissue, and spermine could be detected in trace amounts. Their metabolism is correlated with arginine levels, the most important precursor of putrescine. Polyamine levels increased several fold during the deceleration phase, their increase being positively correlated with increased levels of nucleic acids, mainly during the very beginning of the subculture and, then during the deceleration phase.

1981 ◽  
Vol 59 (11) ◽  
pp. 1969-1977 ◽  
Author(s):  
V. Nuti Ronchi

The histological events leading to shoot formation in Nicotiana glauca and in the nontumorous Nicotiana glauca × Nicotiana langsdorffii hybrid have been studied. Organized development begins from a single vacuolated parenchyma cell which divides and precociously differentiates tracheidal cells, forming a growth center with nodular structures with xylem in the center and phloem outside. The vascular tissue is precociously separated from the surrounding callus by a layer of cells which are shown to be endodermal by position and by histochemical reactions. Further growth leads to the formation of a mound of meristematic tissue which later forms shoot apical meristems. The sequences of events are discussed in relation to other known systems of regeneration in calluses.The system described could be suitable for evaluating the effects of various physical and chemical agents on the different steps of differentiation.


2020 ◽  
Vol 20 (11) ◽  
pp. 821-830
Author(s):  
Prasad Pofali ◽  
Adrita Mondal ◽  
Vaishali Londhe

Background: Current gene therapy vectors such as viral, non-viral, and bacterial vectors, which are used for cancer treatment, but there are certain safety concerns and stability issues of these conventional vectors. Exosomes are the vesicles of size 40-100 nm secreted from multivesicular bodies into the extracellular environment by most of the cell types in-vivo and in-vitro. As a natural nanocarrier, exosomes are immunologically inert, biocompatible, and can cross biological barriers like the blood-brain barrier, intestinal barrier, and placental barrier. Objective: This review focusses on the role of exosome as a carrier to efficiently deliver a gene for cancer treatment and diagnosis. The methods for loading of nucleic acids onto the exosomes, advantages of exosomes as a smart intercellular shuttle for gene delivery and therapeutic applications as a gene delivery vector for siRNA, miRNA and Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) and also the limitations of exosomes as a gene carrier are all reviewed in this article. Methods: Mostly, electroporation and chemical transfection are used to prepare gene loaded exosomes. Results: Exosome-mediated delivery is highly promising and advantageous in comparison to the current delivery methods for systemic gene therapy. Targeted exosomes, loaded with therapeutic nucleic acids, can efficiently promote the reduction of tumor proliferation without any adverse effects. Conclusion: In the near future, exosomes can become an efficient gene carrier for delivery and a biomarker for the diagnosis and treatment of cancer.


2015 ◽  
Vol 51 (37) ◽  
pp. 7887-7890 ◽  
Author(s):  
Hideto Maruyama ◽  
Kazuhiro Furukawa ◽  
Hiroyuki Kamiya ◽  
Noriaki Minakawa ◽  
Akira Matsuda

Synthetic chemically modified nucleic acids, which are compatible with DNA/RNA polymerases, have great potential as a genetic material for synthetic biological studies.


Toxics ◽  
2020 ◽  
Vol 8 (3) ◽  
pp. 51
Author(s):  
Jorge Humberto Limón-Pacheco ◽  
Natalie Jiménez-Barrios ◽  
Alejandro Déciga-Alcaraz ◽  
Adriana Martínez-Cuazitl ◽  
Mónica Maribel Mata-Miranda ◽  
...  

Some studies have shown that silicon dioxide nanoparticles (SiO2-NPs) can reach different regions of the brain and cause toxicity; however, the consequences of SiO2-NPs exposure on the diverse brain cell lineages is limited. We aimed to investigate the neurotoxic effects of SiO2-NP (0–100 µg/mL) on rat astrocyte-rich cultures or neuron-rich cultures using scanning electron microscopy, Attenuated Total Reflection-Fourier Transform Infrared spectroscopy (ATR-FTIR), FTIR microspectroscopy mapping (IQ mapping), and cell viability tests. SiO2-NPs were amorphous particles and aggregated in saline and culture media. Both astrocytes and neurons treated with SiO2-NPs showed alterations in cell morphology and changes in the IR spectral regions corresponding to nucleic acids, proteins, and lipids. The analysis by the second derivative revealed a significant decrease in the signal of the amide I (α-helix, parallel β-strand, and random coil) at the concentration of 10 µg/mL in astrocytes but not in neurons. IQ mapping confirmed changes in nucleic acids, proteins, and lipids in astrocytes; cell death was higher in astrocytes than in neurons (10–100 µg/mL). We conclude that astrocytes were more vulnerable than neurons to SiO2-NPs toxicity. Therefore, the evaluation of human exposure to SiO2-NPs and possible neurotoxic effects must be followed up.


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