AB0135 THE MITOCHONDRIAL-RETICULAR NETWORK (MRN) OF NEUTROPHILIC LEUKOCYTES OF SYNOVIAL FLUID (SF) OF PATIENTS WITH SLE AND RA

2020 ◽  
Vol 79 (Suppl 1) ◽  
pp. 1368.1-1368
Author(s):  
G. V. Kudriavtseva ◽  
Y. Malenkov ◽  
V. Shishkin ◽  
V. V. Shishkin

Background:Objectives:It has been established that in cells, in particular in neutrophilic leukocytes of SF, mitochondria form a mitochondrial-reticular dynamic spatial network (MRN). MRN is the epicenter of apoptosis, reflecting structural and functional changes in the immuno-complex pathology in SLE and RA.Methods:SF was analyzed in patients: 10 SLE (43 ± 2.3 years), 13 RA (45 ± 1.6 years) and 8 donors (42 ± 3.7 years, postmortem). Neutrophilic leukocytes from the SF were isolated by standard methods and resuspended in a composition medium: 70 mM NaCl; 140 mM sucrose; 5.6 mM KCl; 10 mM pyruvate; 8 mM MOPS; pH = 7.4. The cell suspension was centrifuged for 5 min at 800 g. MRN was isolated by centrifuging the resulting supernatant for 15 min at 12 000 g. The resulting MRN fragments were resuspended in citrate-phosphate buffer (pH = 7.4) and used in experiments. The activity of adenosine monophosphate-activated protein kinase (AMPK) was evaluated by Western blotting. Quantitative determination of cytochrome C (Cyt C) was carried out by enzyme immunoassay method using the Human Cytochrome c Platinum ELISA kit (eBioscience, USA). Active forms of oxygen free radicals (AFRF) were registered by EPR. The swelling rate of MRN fragments was determined spectrophotometrically at 540 nm. The electrophoretic mobility (EM) of MRN fragments was determined by the automatic microscope “Parmoquant-2”.Results:MRN of neutrophilic leukocytes of the SF undergoes significant adaptive rearrangements during the development of SLE and RA (tab.1). On average, the expression of biochemical indicators of autophagy (AMPK), apoptosis (Сyt. C), necrosis (level of oxygen free radicals, low-amplitude swelling rate) increases by 2-3 times compared with the conventional norm. Particular attention should be paid to pathological changes in the electrokinetic potential of MRN, which determines the functional state of the SF as a whole as a colloidal system. Obviously, in SLE and RA, depletion of the energy of MRN (a sharp increase in the activity of AMRK), activation of free radical processes, disruption of intracellular ion homeostasis due to an increase in the rate of swelling of MRN as a manifestation of a compensatory-adaptive reaction. It ultimately leads to a decrease in electrokinetic properties of MRN. Thus EM is an integral indicator of physico-chemical properties and architectonics of MRN pointihg to the development of autoimmune pathology.Table 1.EXPRESSION OF INDUCTORS OF AUTOPHAGY, APOPTOSIS, NECROSIS AND ELECTROPHORETIC MOBILITY OF MRN FRAGMENTS OF NEUTROPHILIC LEUKOCYTES OF SF IN SLE AND RAExperience TermsAMPK,cond.unit/mg proteinCyt C,ng/mlAFRF, unit/mg proteinSwelling rate of MRN,/min ·mg proteinEM,m/v · secDonor (8)0,51±0,0523,7±5,47,3±2,40,177± 0,0041,58± 0,07SLE (10)1,73±0,04**49,3±6,5*21,3±5,1**0,435±0,005***0,35±0,05***RA (13)1,25±0,07**47,8±4.8*15,7±4,3*0,410±0,007***0,41±0,07***Notes: differences with the control norm: * - p <0.05; ** - p <0.01; *** - p <0.001.Conclusion:Endoplasmic stress occurs in SF cells during the development of SLE and RA, blocking of autophagy and apoptosis leads to a breakdown of neutrophilic leukocyte MRN, accumulation of high molecular products of tissue decay - phlogogens in the intercellular space, among which the expression in the context is characterized by proteins - chaperones Hsp 60-100. These processes are accompanied by a shift in the bioelectric homeostasis of MRN neutrophilic leukocytes, an increase in their swelling rate and a significant decrease in their electrokinetic potential. The described MRN reactions of neutrophilic leukocytes of the SF should be taken into account when developing pharmacologically induced apoptosis as a new approach in the treatment of autoimmune diseasesReferences:[1]Shishkin V. I. et al. Ann Rheum Dis 2017; 76: No 6, p.1077-1078; DOI:10.1136/annrheumdis-2017-eular5364Disclosure of Interests:None declared

2021 ◽  
Author(s):  
Baozhu Li ◽  
Ruonan Fan ◽  
Guiling Sun ◽  
Ting Sun ◽  
Yanting Fan ◽  
...  

Abstract Background and aims As drought threatens the yield and quality of maize (Zea mays L.), it is important to dissect the molecular basis of maize drought tolerance. Flavonoids, participate in the scavenging of oxygen free radicals and alleviate stress-induced oxidative damages. This study aims to dissect the function of flavonoids in the improvement of maize drought tolerance. Methods Using far-infrared imaging screening, we previously isolated a drought overly insensitivity (doi) mutant from an ethyl methanesulfonate (EMS)-mutagenized maize library and designated it as doi57. In this study, we performed a physiological characterization and transcriptome profiling of doi57 in comparison to corresponding wild-type B73 under drought stress. Results Under drought stress, doi57 seedlings displayed lower leaf-surface temperature (LST), faster water loss, and better performance in growth than B73. Transcriptome analysis reveals that key genes involved in flavonoid biosynthesis are enriched among differentially expressed genes in doi57. In line with these results, more flavonols and less hydrogen peroxide (H2O2) were accumulated in guard cells of doi57 than in those of B73 with the decrease of soil water content (SWC). Moreover, the capacity determined from doi57 seedling extracts to scavenge oxygen free radicals was more effective than that of B73 under the drought treatment. Additionally, doi57 seedlings had higher photosynthetic rates, stomatal conductance, transpiration rates, and water use efficiency than B73 exposed to drought stress, resulting in high biomass and greater root/shoot ratios in doi57 mutant plants. Conclusion Flavonoids may facilitate maize seedling drought tolerance by lowering drought-induced oxidative damage as well regulating stomatal movement.


1986 ◽  
Vol 251 (5) ◽  
pp. F839-F843 ◽  
Author(s):  
M. S. Paller ◽  
R. P. Hebbel

After renal ischemia, oxygen free radicals are formed and produce tissue injury, in large part, through peroxidation of polyunsaturated fatty acids. We used an in vivo method to monitor lipid peroxidation after renal ischemia, the measurement of ethane in expired gas, to determine the time course of lipid peroxidation and the effect of several agents to limit lipid peroxidation after renal ischemia. In anesthetized rats there was no significant increase in ethane production during 60 min of renal ischemia. During the first 10 min of renal reperfusion, there was a prompt increase in ethane production from 2.9 +/- 1.3 to 6.3 +/- 1.9 pmol/min (P less than 0.05). Ethane production was significantly increased during the first 50 min of reperfusion and then rapidly tapered to base-line levels. Preischemic administration of allopurinol to prevent superoxide radical generation or the superoxide radical scavenger superoxide dismutase prevented the increase in ethane production during postischemic reperfusion. These studies confirm that there is increase lipid peroxidation following renal ischemia that can be prevented by agents which limit the formation or accumulation of oxygen free radicals. This in vivo method for measuring lipid peroxidation could also be employed to study the effects of ischemia on lipid peroxidation in other organs, as well as to monitor lipid peroxidation in other forms of injury.


1995 ◽  
Vol 66 (5) ◽  
pp. 473-475 ◽  
Author(s):  
Erol Göktürk ◽  
Akin Turgut ◽  
Cengiz Baygu ◽  
Izge Gunal ◽  
Sinan Seber ◽  
...  

1987 ◽  
Vol 122 (8) ◽  
pp. 961
Author(s):  
BEN EISEMAN

IUBMB Life ◽  
1998 ◽  
Vol 46 (1) ◽  
pp. 207-214 ◽  
Author(s):  
Edmundo Chávez ◽  
Cecilia Zazueta ◽  
Adela Cuéllar ◽  
Horacio Reyes-Vivas ◽  
Noemí García

1991 ◽  
Vol 57 (1-2) ◽  
pp. 1-17 ◽  
Author(s):  
James A. Jesberger ◽  
J. Steven Richardson

1992 ◽  
Vol 111 (1-2) ◽  
Author(s):  
Arshad Rahman ◽  
Fabeha Fazal ◽  
Julie Greensill ◽  
K. Ainley ◽  
J.H. Parish ◽  
...  

Angiology ◽  
1988 ◽  
Vol 39 (12) ◽  
pp. 1005-1013 ◽  
Author(s):  
Kailash Prasad ◽  
Jawahar Kalra ◽  
Greg Buchko

Sign in / Sign up

Export Citation Format

Share Document