Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 6 de 6
Filter
1.
Chinese Journal of Blood Transfusion ; (12): 129-133, 2022.
Article in Chinese | WPRIM | ID: wpr-1004326

ABSTRACT

【Objective】 To investigate the quality changes of suspended red blood cells (SRBCs) prepared from the blood of Tibetan high Hb population, and explore the availability and safety of blood collected from Tibetan high Hb population. 【Methods】 The voluntary blood donors were grouped according to the Hb concentration at the initial screening: female blood donors from Tibet Autonomous Region (>3 500 m) with Hb≥190 g/L and male blood donors with Hb≥210 g/L were classified as plateau high hemoglobin group. A total of 13 male blood donors from Tibet Autonomous Region were recruited. And the female blood donors (n=13) with Hb(115~165) g/L and male blood donors (n=12) with Hb(120~185) g/L from Chengdu were classified as control group. Whole blood of 200 mL specification was centrifuged to remove the plasma, and MAP additive solution was added to prepare SRBCs, then SRBCs were divided into four aliquots (50 mL/bag and stored at 4℃. Parameters as blood routine, free Hb and hemolysis rate were measured aseptically at day 1, 14, 21, 35 of storage. And 10 mL SRBCs was used to extract membrane proteins for tyrosine phosphorylation detection of band 3 protein. 【Results】 The RBCs counts(×1012/L), hematocrit(%) and hemoglobin(g/L) of Tibetan high Hb group and control group were 6.76±0.95 vs 4.65±0.52, 63.3±6.8 vs 43.1±4.4 and 214.4±19.8 vs 143.2±16.9 (P<0.01). The erythrocyte deformability test on the day 1, 14, 21, 35 of storage showed that the deformability of SRBCs prepared from Tibetan high Hb group was significantly lower than that of the control group under shear stress of 3, 5.33, 9.49, 16.87, and 30 Pa, while the hemolysis rate of SRBCs prepared from the Tibetan high Hb group and the control group on the day 1, 14, 21, 35 were 0.050 2±0.040 2 vs 0.022 2±0.011 1, 0.055 4±0.043 vs 0.032 1±0.028 7, 0.061 2±0.025 9 vs 0.034 3±0.031 7 and 0.069 6±0.032 0 vs 0.044 0±0.033 3 (P<0.05). Western blotting showed that the cytoplasmic N-terminal Y21 of band 3 protein of SRBCs prepared from Tibetan high Hb group was highly phosphorylated. 【Conclusion】 The deformability of SRBCs prepared from the Tibetan high Hb group was significantly lower while the hemolysis rate of SRBCs was higher than that of the control group. The hemolysis rate of the SRBCs at the end of storage prepared from the Tibetan high Hb group meets the requirements of the national standard GB18469-2012(<0.8%). The increase of hemolysis rate of SRBCs prepared from the Tibetan high Hb group was closely related to the phosphorylation of band 3 protein.

2.
Article in Spanish | LILACS | ID: lil-628523

ABSTRACT

Se determinó la presencia de anticuerpos naturales anti banda 3 mediante un ensayo inmunoenzimático en microplacas acopladas con la proteína banda 3 en 14 pacientes con drepanocitosis, 4 con crisis vasooclusiva dolorosa y 10 en estado basal. Se demostró una disminución significativa (p = 0,000005) de los niveles de los anticuerpos naturales anti banda 3 en el total de los pacientes al compararlos con los controles normales, lo que puede estar relacionado con un consumo elevado de estos en el proceso de aclaramiento de eritrocitos con hemoglobina SS oxidados o senescentes. No se demostró diferencia estadística entre el grupo de pacientes en estado basal y aquellos con crisis vasooclusiva dolorosa, lo cual sugiere la posibilidad de que no haya participación de los anticuerpos naturales anti banda 3 en la modulación del fenómeno oclusivo que se produce en esta enfermedad. Se recomienda el estudio longitudinal de un número mayor de pacientes, que permita profundizar en este aspecto.


The presence of natural anti-band 3 antibodies was determined by an immunoenzymatic assay in microplaques coupled with band 3 protein in 14 patients with drepanocytosis, 4 with painful vasoocclusive crisis and 10 in the basal state. It was proved a significant reduction (p = 0,000005) of the levels of natural anti-band 3 antibodies in all the patients on comparing them with the normal controls, which may be related to an elevated consumption of these in the clearance process of oxidized or senescent erythrocytes with hemoglobin SS. There was no statistical difference between the group of patients in the basal state and those with painful vasoocclusive crisis, which suggests that the natural anti-band 3 antibodies do not take part in the modulation of the occlusive phenomenon that is produced in this disease. The longitudinal study of a greater number of patients that allows to go deep into this apect is recommended.

3.
Journal of Veterinary Science ; : 329-333, 2007.
Article in English | WPRIM | ID: wpr-117486

ABSTRACT

The purpose of this study was to determine the expression and distribution of band 3 in the collecting duct and connecting tubules of the kidney of the marmoset monkey (Callithrix jacchus), and to establish whether band 3 is expressed in type A intercalated cells. The intracellular localization of band 3 in the different populations of intercalated cells was determined by double-labeling immunohistochemistry. Immunohistochemical microscopy demonstrated that band 3 is located in the basolateral plasma membranes of all type A intercalated cells in the connecting tubule (CNT), cortical collecting duct (CCD), and outer medullary collecting duct (OMCD) of the marmoset. However, type B intercalated cells and non-A/ non-B intercalated cells did not show band 3 labeling. Electron microscopy of the CNT, CCD and OMCD confirmed the light microscopic observation of the basolateral plasma membrane staining for band 3 in a subpopulation of interacted cells. Basolateral staining was seen on the plasma membrane and small coated vesicles in the perinuclear structure, some of which were located in the Golgi region. In addition, there was no labeling of band 3 in the mitochondria of the CNT, CCD and in OMCD cells. The intensity of the immunostaining of the basolateral membrane was less in the CNT than in the CCD and OMCD. In contrast, band 3 immunoreactivity was greater in the intracellular vesicles of the CNT. From these results, we suggest that the basolateral Cl-/HCO3- exchanger in the monkey kidney is in a more active state in the collecting duct than in the CNT.


Subject(s)
Animals , Male , Anion Exchange Protein 1, Erythrocyte/metabolism , Callithrix/metabolism , Gene Expression Profiling/veterinary , Gene Expression Regulation , Immunohistochemistry/veterinary , Kidney Tubules/cytology , Kidney Tubules, Collecting/cytology , Microscopy, Electron, Transmission/veterinary
4.
Korean Journal of Nephrology ; : 899-909, 2000.
Article in Korean | WPRIM | ID: wpr-9255

ABSTRACT

The purpose of this study was to elucidate whether the molecular defect of acid-base transporters in renal tubules is related to the functional defect of urinary acidification in distal renal tubular acidosis(RTA). We performed NH4Cl, furosemide, or bicarbonate loading test to evaluate renal acidification function, and immunohistochemistry using antibodies to H+- ATPase, Cl-/HCO3- exchanger(band-3 protein), and Na+/K+-ATPase in kidney tissue in 6 patients with RTA and renal cell carcinoma patients as normal controls. Kidney tissue was obtained either by percutaneous needle biopsy(RTA) or nephrectomy(NC). The results were as follows; 1) In all six RTA patients, proton secretory defect of distal acidification was shown by a failure to lower the urine pH after NH4Cl loading or furosemide test or abnormally low urine-blood pCO2 difference during bicarbonate loading. In two patients with RTA, proximal acidification defect was combined, which was demonstrated by increased fractional excretion of bicarbonate. 2) In normal control, intense H+-ATPase and band-3 protein staining was observed in collecting ducts. 3) In distal RTA patients, H+-ATPase and band- 3 protein staining was not demonstrable or markedly decreased in the intercalated cells of distal nephron. 4) In two patients who had both proximal and distal RTA, H+-ATPase staining was markedly decreased in the brush border of proximal tubules as well as the distal nephron. In conclusion, the defect of acid-base transporters in renal tubule was related with the functional defect of urinary acidification in distal RTA.


Subject(s)
Humans , Acidosis, Renal Tubular , Adenosine Triphosphatases , Antibodies , Carcinoma, Renal Cell , Furosemide , Hydrogen-Ion Concentration , Immunohistochemistry , Kidney , Microvilli , Needles , Nephrons , Protons
5.
Journal of Third Military Medical University ; (24)1988.
Article in Chinese | WPRIM | ID: wpr-550659

ABSTRACT

The changes of erythrocytic membrane band 3 protein and intraery-throcytic and extrar rythrccytic gases and electrolytes were studied in 69 cases of cor pulmonale and 50 normal subjects.It was found that in the patients of cor pulmonale accompanied with type Ⅱ respiratory failure,the relative low level of erythrocytic membrane band 3 protein and the restriction of HCO-3/Cl-exchange were the factors to aggravate CO2 retention and respiratory acidosis,relative intraerythrocytic alkalosis resulted from the relative increase of intra-erythrocytic HCO-3([HCO-3]),and prompt adminstration of oxygen to cor pulmonale patients with hypoxemia could not only improve extraerythrocytic acid-base imbalance but also increase intraerythcocytic P5O2 and the tissue capacity to store oxygen.

6.
Academic Journal of Second Military Medical University ; (12)1981.
Article in Chinese | WPRIM | ID: wpr-549833

ABSTRACT

To study the effect of iron deficiency (ID)on crythrocyte membrane proteins, an investigation of the activity and site of Na+-K+-ATPase in crythrocyte membrane of rats with iron deficient anemia (IDA) was conducted. It was found that changes of the enzyme activity had various ciiaracteristics as ID course went on, and there was no difference in the numbers of 3H-ouabain binding sites (R0) between IDA rats and controls. In contrast to the controls, Na+-K+- ATPase activity of IDA rats showed no relation with R0, suggesting a primary association of the abnormalized activity of the enzyme with its molecular state in ID erythrocyte membrane which could be affected by the surroundings of cell metabolism and spatial structure.

SELECTION OF CITATIONS
SEARCH DETAIL