1.Changes of adhesion molecules and adenosine in divers post 480 heliox saturation diving.
Xiao-Chen BAO ; Yi-Quna FANG ; Jun MA ; Miao MENG ; Wei-Bing XIAO
Chinese Journal of Applied Physiology 2012;28(5):422-424
<p>OBJECTIVETo investigate the changes of adhesion molecules, cyclic adenosine monophosphate(cAMP) and cyclic guanosine monophosphate (cGMP) in divers post 480 heliox saturation diving.p><p>METHODSFour divers were compressed within 96 hours to depths of 480 m with heliox-oxygen and held at the designated depth for 49 hours, excursion to 493 m during their saturation stay, then decompressed within 302 hours to the surface. The blood samples were collected before compression and post decompression, the expression level of intercellular adhesion molecule-1(ICAM-1), E-selectin, P-selectin, cAMP, cGMP were detected with ELISA analysis box.p><p>RESULTSCompared with the levels of CAMs before compression, the levels of ICAM-1, E-selectin, P-selectin and cGMP in the serum were changed post decompression (P > 0.05). The levels of cAMP were significantly elevated post decompression (629.91 +/- 75.01) nmol/L vs (66.72 +/- 83.15) (P < 0.05).p><p>CONCLUSIONThe decompression schedule in this heliox saturation diving is safe, the decompression sickness pathology in this diving has not been induced. But the stress response of divers are enhanced by this great depth saturation diving.p>
Cyclic AMP
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blood
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Diving
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physiology
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E-Selectin
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blood
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Helium
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Humans
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Intercellular Adhesion Molecule-1
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blood
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Oxygen
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P-Selectin
;
blood
2.Activation of random-donor platelet concentrates and platelet prepared from random-donor apheresis collections during storage.
Jun-Jie LIN ; Hua-Hua FAN ; Qing MA ; Ming-Liang FENG ; Xing-Feng SHEN
Journal of Experimental Hematology 2002;10(5):458-461
The activation of random-donor platelet concentrates and platelets prepared from random-donor apheresis collections (plateletpheresis) during storage were studied. Percentage of CD62p staining and mean channel fluorescence (MCF) of CD41 of two kinds of platelets during storage on day 0, day 1, day 3 and day 5 were determined by flow cytometry. The results showed that percentages of CD62p staining and MCF of CD41 in plateletpheresis were (18.91 +/- 6.25)%, (19.48 +/- 8.27)%, (22.82 +/- 6.06)%, (56.71 +/- 11.79)% and (8.09 +/- 2.38)%, (8.13 +/- 2.45)%, (8.44 +/- 2.51)%, (19.87 +/- 6.13)%, while the results of platelet concentrates were (30.65 +/- 12.33)%, (31.46 +/- 11.86)%, (32.51 +/- 13.05)%, (63.55 +/- 13.27)% and (10.33 +/- 4.37)%, (11.09 +/- 6.61)%, (13.46 +/- 9.69)%, (24.41 +/- 10.15)%, respectively. The platelet count and pH value were also determined. The platelet number, pH value, percentage of CD62p staining and MCF of CD41 had no significant difference within 3 days of platelet storage. The platelet number and pH value decreased significantly (P < 0.001), while percentages of CD62p staining and MCF of CD41 increased significantly (P < 0.001) on day 5 of storage. It is concluded that the quality of plateletpheresis is better than platelet concentrate.
Blood Donors
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Blood Preservation
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Humans
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P-Selectin
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blood
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Platelet Activation
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Platelet Membrane Glycoprotein IIb
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blood
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Plateletpheresis
3.Modified flow cytometry assay for CD62p expression of preserved platelets.
Xi-Lin OUYANG ; Jing-Han LIU ; Qun SHI ; Da-Yong GAO
Journal of Experimental Hematology 2002;10(5):462-465
CD62p expression was an important monitoring parameter for preserved platelets quality. To setup an optimized flow cytometry assay for preserved platelets based on the CD62p expression on platelets, the platelet samples were collected, 0.1 mmol/L persantine and 1.1 mmol/L EDTA were added into the modified TB S used to replace PBS dilution; the methodological evaluation were carried out. Results showed that 0.1 mmol/L persantine and 1.1 mmol/L EDTA achieved to prevent platelets activation during the test procedure. The favorable negative or positive samples were prepared for check of fluorescence antibody's quality to ensure the validity of results. CD61 was used to identify platelets for assay and improve veracity of assay. The special injector was also replaced by special big syringe needle for blood collection to reduce in vitro artifacts, and the prepared sample can be steady-going for 48 hours at 4 degrees C after fixed by 1% paraformaldehyde. It is concluded that this flow cytometry assay for CD62p positive platelets is simple and efficient.
Blood Platelets
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chemistry
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Blood Preservation
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Flow Cytometry
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methods
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Humans
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P-Selectin
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blood
4.Change of platelet count and P-selectin in preserved platelet concentrates.
Hui-Fang NIE ; Bao-Qing LUI ; Run-Ling ZHANG ; Yu-Chun ZHANG ; Zhi-Feng ZHANG ; Chun-Fang YUAN
Journal of Experimental Hematology 2002;10(6):571-573
To observe the change of quantity and quality of platelets preserved in a full-sealed bag, and explore the difference of platelets preserved in oscillating and static conditions at (22 +/- 2) degrees C, the platelet concentrates were prepared with a CS-3000-plus blood cell separator, the platelet counts were performed with automatic blood cell analyzer and P-selectin in supernatant of platelet concentrates was detected by ELISA. The results showed that both of platelet count and P-selectin content in the platelet concentrates had no significant difference between oscillating and static preservation condition. With prolongation of preserved time, the platelet count decreased and P-selectin content increased gradually in both preserved conditions. There was no difference in the platelet counts during 0 - 72 hours preservation in both conditions, and significant difference was seen in 96 - 120 hours preservation. It was concluded that the expired date for platelet product preserved in CS-3000-plus blood cell separator full-sealed system should be 3 days. Under the condition of (22 +/- 2) degrees C, the quality of the platelet preserved in oscillating state is not superior to static preservation.
Blood Platelets
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chemistry
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Blood Preservation
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Female
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Humans
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Male
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P-Selectin
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blood
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Platelet Count
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Time Factors
5.Expression and significance of adhesion molecules CD62P and CD44 in peripheral blood of infants with bronchiolitis.
Li-Ping ZOU ; Wei WANG ; Yan-Li ZHANG ; Yan ZHANG ; Li WANG
Chinese Journal of Contemporary Pediatrics 2015;17(11):1200-1203
<p>OBJECTIVETo explore the expression and significance of the adhesion molecules CD62P and CD44 in the peripheral blood of infants with bronchiolitis.p><p>METHODSThirty-three infants with bronchiolitis in the acute phase and 19 infants with bronchiolitis in the recovery phase, who were hospitalized between November 2014 and May 2015, were enrolled. Thirty infants with bronchopneumonia and 26 infants without infection were enrolled as the bronchopneumonia group and the control group, respectively. The CD62P expression in the peripheral blood of each group was measured by flow cytometry, and the CD44 level in serum was determined using ELISA.p><p>RESULTSThe levels of the adhesion molecules CD62P and CD44 in the bronchiolitis group in the acute phase were significantly higher than those in the bronchiolitis group in the recovery phase, the bronchopneumonia group, and the control group (P<0.05). The levels of the adhesion molecules CD62P and CD44 in the bronchiolitis group in the recovery phase were also significantly higher than those in the control group (P<0.05). In the bronchiolitis group in the acute phase, there was a positive correlation between CD62P expression and serum CD44 level (r=0.91; P<0.05).p><p>CONCLUSIONSThe adhesion molecules CD62P and CD44 play an important role in the pathogenesis of bronchiolitis, and their levels can reflect the severity of inflammatory response in infants with bronchiolitis.p>
Bronchiolitis
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blood
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etiology
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Female
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Humans
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Hyaluronan Receptors
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blood
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physiology
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Infant
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Male
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P-Selectin
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blood
;
physiology
6.Increased Serum Level of P-Selectin in Patients with Lichen Planus.
Teoman ERDEM ; A Ihsan GULEC ; Akin AKTAS ; Abdulkadir YILDIRIM ; Ahmet KIZILTUNC
Yonsei Medical Journal 2004;45(2):215-218
Lichen planus (LP) is a common, pruritic and inflammatory disease of the skin, hair follicles and mucous membranes. Immunologic mechanisms, especially cell-mediated immunity, play a major role in triggering the clinical expression of the disease. P-selectin is an adhesion molecule present within endothelial cells and mediates endothelial-leukocyte interactions. Therefore, it is considered that P-selectin plays an important role in LP. The aim of our study is to research the relation between P-selectin and LP. Serum P-selectin levels were determined with the enzyme- linked immunosorbent sandwich assay method in sera from 40 LP patients and 40 healthy controls. The serum levels of P-selectin were statistically significantly higher in the patients than in healthy controls (p < 0.05), in female patients (39.32 +/- 11.34 pg/ml) than in male patients (31.93 +/- 9.83 pg/ml) (p < 0.01), and in the patients with eruptive form (40.27 +/- 9.32 pg/ml) than in those with the localised (32.83 +/- 9.93 pg/ml) and hypertrophic (31.72 +/- 8.39 pg/ml) forms (both p < 0.01). In conclusion, we found a meaningful relation between LP and serum P-selectin levels.
Adult
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Biological Markers
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Female
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Human
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Lichen Planus/*blood/immunology
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Male
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Middle Aged
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P-Selectin/*blood
7.CD62p expression in platelet during the preparation course of Cryopreservated platelet-rich plasma.
Jing-Han LIU ; Xi-Lin OUYANG ; Qun SHI ; Qun LUO ; Xi-Jin LI ; Hai-Bao WANG ; Min-Cai CHENG ; Wei HAN ; Dayong GAO
Journal of Experimental Hematology 2002;10(3):253-256
In order to explore the factors that affect CD62p expression in platelet during the whole course of cryopreservated platelets preparation, CD62p expression of platelet was evaluated by flow cytometry assay. The whole course of cryopreservated platelets preparation in order included whole blood collection, centrifugation for fresh platelet-rich plasma preparation, addition of dimethyl sulfoxide, and freeze in -80 degrees C refrigerator and thaw in 38 degrees C water bath. Result showed that the CD62p expressed slowly from whole blood collection to addition of dimethyl sulfoxide, but expressed abruptly after freeze and thaw and it occupied 82 per cent of the whole expression. It was concluded that the whole blood collection, centrifugation for fresh platelet enriched plasma preparation and addition of dimethyl sulfoxide were optimized in the whole course, but the damage to platelets in the whole course of cryopreservation could not be avoided. It suggests that improved techniques are needed to reduce the damage to cryopreservated platelets.
Blood Platelets
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metabolism
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Blood Preservation
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methods
;
standards
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Cryopreservation
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methods
;
standards
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Flow Cytometry
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Humans
;
P-Selectin
;
biosynthesis
8.Levels of soluble adhesion molecules in patients with various clinical presentations of coronary atherosclerosis.
Hui-He LU ; Zheng-Qiang SHENG ; Yi WANG ; Li ZHANG
Chinese Medical Journal 2010;123(21):3123-3126
<p>BACKGROUNDAdhesion molecules play an important role in the development and progression of coronary atherosclerosis. The aim of this study was to compare concentrations of soluble forms of adhesion molecules in patients with different clinical presentations of coronary artery disease (CAD).p><p>METHODSOne hundred and twenty-eight patients with CAD were divided into three groups; the first group was acute myocardial infarction group (AMI group, n = 45), the second group was unstable angina pectoris group (UAP group, n = 48), the third group was stable angina pectoris group (SAP group, n = 35). We compared them with patients with normal coronary arteries (control group, n = 31). The serum levels of vascular cell adhesion molecule (VCAM-1), intercellular adhesion molecule-1 (ICAM-1), E-selectin and P-selectin were measured in all subjects.p><p>RESULTSThe serum level of VCAM-1 in the AMI group was significantly higher than in the UAP, SAP and control groups (P < 0.01). The level in the UAP group was significantly higher than the SAP group and control group (P < 0.01) and the level in the SAP group was significantly higher than in the control group (P < 0.01). The serum ICAM-1 level was significantly elevated in the AMI, UAP and SAP groups as compared to the control group (P < 0.01). The levels of serum E-selectin and P-selectin in the AMI and UAP groups were significantly higher than in the SAP and control groups (P < 0.01).p><p>CONCLUSIONSIncreased levels of VCAM-1 and ICAM-1, E-selectin and P-selectin, as markers of inflammation, showed the importance of inflammatory processes in the development of atherosclerosis and clinical expression of CAD. Soluble ICAM-1, VCAM-1, E-selectin and P-selectin concentrations are useful indicators of the presence of atherosclerosis and the severity of CAD clinical presentation.p>
Coronary Artery Disease
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blood
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pathology
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E-Selectin
;
blood
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Female
;
Humans
;
Intercellular Adhesion Molecule-1
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blood
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Male
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Middle Aged
;
P-Selectin
;
blood
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Vascular Cell Adhesion Molecule-1
;
blood
9.The Change of PAC-1 and P-selectin Expression after Initiation of Antiplatelets in Patients with Acute Ischemic Stroke.
Sun Ah PARK ; Eun Young KIM ; Sung Rye HA ; Jeong Ho PARK ; Tae Kyeong LEE ; Ki Bum SUNG ; Choon Sik PARK
Journal of the Korean Neurological Association 2006;24(3):210-214
BACKGROUND: The purpose of this study was to evaluate the time course of PAC-1 and the P-selectin expression after the initiation of antiplatelets in acute ischemic stroke. METHODS: We serially measured PAC-1 and the P-selectin expression level using flow cytometry immediately before and at: one day, seven days, and one month after starting antiplatelets in 25 patients with acute cerebral infarctions. RESULTS: The P-selectin expression increased initially (p<0.05) and then from the seventh day, it began to decrease continually (post-hoc analysis, p<0.05). However, the PAC-1 expression did not reveal significant alterations during the follow-up period of one month. CONCLUSIONS: Although the P-selectin expression rapidly declined, the PAC-1 expression remained elevated for one month. Our results suggest that the P-selectin may be useful in monitoring platelet inhibition during the early period after cerebral infarction.
Blood Platelets
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Cerebral Infarction
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Flow Cytometry
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Follow-Up Studies
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Humans
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P-Selectin*
;
Stroke*
10.Flow cytometry combined assay for phosphatidylserine and CD62p expressed by preserved platelets.
Xi-Lin OUYANG ; Jing-Han LIU ; Qun LUO ; Qun SHI ; Wei HAN ; Xi-Jin LI ; Dayong GAO
Journal of Experimental Hematology 2002;10(1):66-69
Human platelets have distinct characters when preserved by different methods. A efficient flow cytometric assay for different preserved platelets expression of CD62p and phosphatidylserine(PS) is in dire need. Efficient flow cytometric assay for CD62p and PS expressed by preserved platelets was established and the major conditions were optimized. The platelets need not to be washed to wipe off plasma and can be labelled diredtly during the sample preparation. It is efficient for flow cytometric analysis when fresh platelet riched plasma (FPRP) was set as negative control, thrombin actived FPRP, and liquid nitrogen treated FPRP were set as positive control respectively. Gly-Pro-Arg-Pro acetate salt (GPRP) was applied to prevent platelets aggregation and fibrin formation, stabilize platelets and minimize the artificial platelets activation. This is also the key to conquer difficulty of flow cytometric quantitive analysis when platelet, Ca(2+) and plasma coexist. This flow cytometric method is specially suitable for the multi-parameter assay including PS expression for cryopreserved platelets. Minimal sample manipulation, no fixation, and GPRP application resulted in minor artifacts and good sample stability. Results suggested, this flow cytometric assay for preserved platelets is simple and efficient. In addition, the author prepared four different methods treated platelets that can be easily distinguished through this flow cytometric assay. It not only makes sure the practicability of this flow cytometric assay, but also suggests the value of the treated platelets applied in preserved platelets flow cytometric ass
Blood Platelets
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metabolism
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Flow Cytometry
;
methods
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Humans
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P-Selectin
;
biosynthesis
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Phosphatidylserines
;
analysis
;
Reproducibility of Results
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Tissue Preservation