1.Role and mechanism of long non-coding RNA HSFAS in hypertrophic scar analyzed using RNA pull-down combined mass spectrometry
Tongtong XIA ; Fang MA ; Haoyuan SUN ; Honglin LIU ; Zhenghao ZHANG ; Jiaqi YANG ; Huiping ZHANG ; Kai WU ; Jiangyong SHEN ; Yideng JIANG ; Guizhong LI
Chinese Journal of Tissue Engineering Research 2025;29(12):2492-2499
BACKGROUND:Previous studies found that the proliferative scar-specific long non-coding RNA lncRNA HSFAS is a novel biomarker that can be used in the diagnosis of hypertrophic scar,but how it functions in hypertrophic scar is not clear. OBJECTIVE:To investigate the role and mechanism of lncRNA HSFAS in hypertrophic scar.METHODS:Fresh scar tissue and surrounding normal skin tissue samples from three patients with hypertrophic scar were collected,and tissue immunofluorescence was used to detect the expression of lncRNA HSFAS in frozen sections of two skin tissues. Primary fibroblasts were isolated from proliferative scarred skin tissue and normal skin tissue and cultured by enzyme digestion method. Quantitative real-time PCR was used to detect the mRNA expression of lncRNA HSFAS in cells. The proteins bound to lncRNA HSFAS were detected by RNA pull-down combined mass spectrometry. GO and KEGG were used to analyze the main functions and pathways of lncRNA HSFAS involved in hypertrophic scar progression. The targeted binding of lncRNA HSFAS to proteins was determined by catRAPID and RPISeq website analysis. RESULTS AND CONCLUSION:Compared with normal skin tissue and fibroblasts from normal skin tissue,the expression of lncRNA HSFAS in human hypertrophic scar tissue and primary fibroblasts from hypertrophic scar tissue was significantly increased (P<0.05). There were 510 proteins clearly bound to lncRNA HSFAS by RNA pull-down combined mass spectrometry. The results of GO and KEGG analyses showed that these proteins were mainly involved in RNA splicing and processing,chromosome synthesis and separation,and cell cycle. Among them,the proteins involved in RNA splicing and processing included scaffold attachment factor B2 and DICER1,and the binding fraction with lncRNA HSFAS was higher. The results of bioinformatics analysis showed that lncRNA HSFAS was bound to scaffold attachment factor B2 and DICER1 proteins. To conclude,lncRNA HSFAS may affect gene expression by interacting with scaffold attachment factor B2 and DICER1 proteins to regulate RNA splicing and processing modification,thus promoting the occurrence and development of hypertrophic scar.
2.Role and mechanism of long non-coding RNA HSFAS in hypertrophic scar analyzed using RNA pull-down combined mass spectrometry
Tongtong XIA ; Fang MA ; Haoyuan SUN ; Honglin LIU ; Zhenghao ZHANG ; Jiaqi YANG ; Huiping ZHANG ; Kai WU ; Jiangyong SHEN ; Yideng JIANG ; Guizhong LI
Chinese Journal of Tissue Engineering Research 2025;29(12):2492-2499
BACKGROUND:Previous studies found that the proliferative scar-specific long non-coding RNA lncRNA HSFAS is a novel biomarker that can be used in the diagnosis of hypertrophic scar,but how it functions in hypertrophic scar is not clear. OBJECTIVE:To investigate the role and mechanism of lncRNA HSFAS in hypertrophic scar.METHODS:Fresh scar tissue and surrounding normal skin tissue samples from three patients with hypertrophic scar were collected,and tissue immunofluorescence was used to detect the expression of lncRNA HSFAS in frozen sections of two skin tissues. Primary fibroblasts were isolated from proliferative scarred skin tissue and normal skin tissue and cultured by enzyme digestion method. Quantitative real-time PCR was used to detect the mRNA expression of lncRNA HSFAS in cells. The proteins bound to lncRNA HSFAS were detected by RNA pull-down combined mass spectrometry. GO and KEGG were used to analyze the main functions and pathways of lncRNA HSFAS involved in hypertrophic scar progression. The targeted binding of lncRNA HSFAS to proteins was determined by catRAPID and RPISeq website analysis. RESULTS AND CONCLUSION:Compared with normal skin tissue and fibroblasts from normal skin tissue,the expression of lncRNA HSFAS in human hypertrophic scar tissue and primary fibroblasts from hypertrophic scar tissue was significantly increased (P<0.05). There were 510 proteins clearly bound to lncRNA HSFAS by RNA pull-down combined mass spectrometry. The results of GO and KEGG analyses showed that these proteins were mainly involved in RNA splicing and processing,chromosome synthesis and separation,and cell cycle. Among them,the proteins involved in RNA splicing and processing included scaffold attachment factor B2 and DICER1,and the binding fraction with lncRNA HSFAS was higher. The results of bioinformatics analysis showed that lncRNA HSFAS was bound to scaffold attachment factor B2 and DICER1 proteins. To conclude,lncRNA HSFAS may affect gene expression by interacting with scaffold attachment factor B2 and DICER1 proteins to regulate RNA splicing and processing modification,thus promoting the occurrence and development of hypertrophic scar.
3.Characteristics of Effective Pacing Strategies of 1 500-m Freestyle Medalists in World Swimming Championships
Xiaoqing LÜ ; Haoyuan WU ; Lewen HONG ; Ming LI ; Xuhong LI
Journal of Medical Biomechanics 2024;39(6):1168-1174
Objective To explore whether the medalists in 1 500-m freestyle swimming choose different pacing strategies from their competitors,so as to determine the most effective pacing strategy characteristics to obtain victory in swimming race.Methods The 1 500-m freestyle finalists in World Swimming Championships from 2003 to 2023 were selected as candidates of this study.According to the final ranking of the 175 elite athletes in the race,the split time,cumulative time were calculated,respectively.The differences of the main indicators in pacing strategies between medalists and their competitors were compared,and the above variables were selected for one-way ANOVA statistical analysis.Results The medalists had a significant speed advantage regardless of split time in the race,as well as the velocity of the starting stage,intermediate swim and end spurt(P<0.01).After the normalization of the cumulative time,the differences between the medalists and 4th-8th athletes in the percentage of split time and normalized velocity were mainly reflected in the last 400 m or so of the first and second half of the race(P<0.05).Regardless of whether they won medals or not,the pacing strategies of male freestyle swimmers were mostly reverse J-and U-shaped,while those of the female were mainly reverse J-shaped(90.9%).The diving start indicator(DSI)and end-spurt indicator(ESI)of medalists were higher,but the ESI of medalists was significantly different from that of 4th-8th athletes(P<0.05).Meanwhile,the coefficient of variation(CV)and the median and quartile of the density distribution of CV were significantly lower in intermediate stage.Conclusions All 1 500-m freestyle finalists follow a similar parabolic pacing strategies regardless of gender and final race ranking.Compared with their competitors,the medalists choose a relatively conservative starting strategy,a more even pace through the middle section of the race and a strong end-spurt.In summary,the reverse J-shape is an effective pacing strategy for the success of elite freestyle athletes in 1 500-m swimming competitions.
4.Characteristics of Effective Pacing Strategies of 1 500-m Freestyle Medalists in World Swimming Championships
Xiaoqing LÜ ; Haoyuan WU ; Lewen HONG ; Ming LI ; Xuhong LI
Journal of Medical Biomechanics 2024;39(6):1168-1174
Objective To explore whether the medalists in 1 500-m freestyle swimming choose different pacing strategies from their competitors,so as to determine the most effective pacing strategy characteristics to obtain victory in swimming race.Methods The 1 500-m freestyle finalists in World Swimming Championships from 2003 to 2023 were selected as candidates of this study.According to the final ranking of the 175 elite athletes in the race,the split time,cumulative time were calculated,respectively.The differences of the main indicators in pacing strategies between medalists and their competitors were compared,and the above variables were selected for one-way ANOVA statistical analysis.Results The medalists had a significant speed advantage regardless of split time in the race,as well as the velocity of the starting stage,intermediate swim and end spurt(P<0.01).After the normalization of the cumulative time,the differences between the medalists and 4th-8th athletes in the percentage of split time and normalized velocity were mainly reflected in the last 400 m or so of the first and second half of the race(P<0.05).Regardless of whether they won medals or not,the pacing strategies of male freestyle swimmers were mostly reverse J-and U-shaped,while those of the female were mainly reverse J-shaped(90.9%).The diving start indicator(DSI)and end-spurt indicator(ESI)of medalists were higher,but the ESI of medalists was significantly different from that of 4th-8th athletes(P<0.05).Meanwhile,the coefficient of variation(CV)and the median and quartile of the density distribution of CV were significantly lower in intermediate stage.Conclusions All 1 500-m freestyle finalists follow a similar parabolic pacing strategies regardless of gender and final race ranking.Compared with their competitors,the medalists choose a relatively conservative starting strategy,a more even pace through the middle section of the race and a strong end-spurt.In summary,the reverse J-shape is an effective pacing strategy for the success of elite freestyle athletes in 1 500-m swimming competitions.
5.Rac1 promotes the formation of heterotypic cell-in-cell structure.
Tao HU ; Pengfei FENG ; Haoyuan LI ; Lulin ZHOU ; Zubiao NIU ; Yinuo HUANG ; Xiaoning WANG ; Chenxi WANG ; Hui LIU ; Chengjun WU
Chinese Journal of Biotechnology 2023;39(10):4123-4134
Heterotypic cell-in-cell structures (heCICs) are closely related to tumor development and progression, and have become a new frontier in life science research. Ras-related C3 botulinum toxin substrate 1 (Rac1) belongs to the classic Rho GTPase, which plays a key role in regulating the cytoskeleton and cell movement. To investigate the role and mechanism of Rac1 in the formation of heCICs, tumor cells and immune killer cells were labeled with cell-tracker, respectively, to establish the heCICs model. Upon treatment with the Rac1 inhibitor NSC23766, the formation of heCICs between tumor and immune cells was significantly reduced. The plasmid pQCXIP-Rac1-EGFP constructed by gene cloning was packaged into pseudoviruses that subsequently infect tumor cells to make cell lines stably expressing Rac1. As a result, the formation of heCICs was significantly increased upon Rac1 overexpression. These results demonstrated a promotive role of Rac1 in heCICs formation, which may facilitate treating cell-in-cell related diseases, such as tumors, by targeting Rac1.
6.Relationship between serum FABP1,FABP2 levels and diabetic kidney disease in patients with type 2 diabetes mellitus
Meiyue LYU ; Ling WANG ; Yu WU ; Haoyuan SUN ; Lin ZHANG
International Journal of Laboratory Medicine 2023;44(24):3016-3020,3026
Objective To investigate the relationship between serum fatty acid binding protein(FABP)1,FABP2 and diabetic kidney disease(DKD)in patients with type 2 diabetes mellitus(T2DM)and its diagnostic value.Methods A total of 170 patients with T2DM diagnosed and treated in this hospital from January 2020 to December 2022 were selected as the research objects.According to urinary albumin to creatinine ratio(UACR),they were divided into non-DKD group(UACR<30 mg/g,72 cases)and DKD group(UACR≥30 mg/g,98 cases).A total of 60 healthy people in the same hospital during the same period were selected as the control group.Pearson correlation analysis was used to analyze the correlation between serum FABP1,FABP2 and renal function related indicators.Multivariate Logistic regression was used to analyze the influencing fac-tors of DKD.Receiver operating characteristic curve was used to evaluate the diagnostic efficacy of serum FABP1 and FABP2 for DKD.Results The DKD group had significantly higher serum levels of FABP1 and FABP2 than the non-DKD group and the control group(P<0.05),and the non-DKD group had significantly higher serum levels of FABP1 and FABP2 than the control group(P<0.05).Compared with the non-DKD group,the DKD group had a significantly lower eGFR and significantly higher UACR,serum creatinine,blood urea nitrogen,and serum uric acid levels(P<0.05).Serum FABP1 and FABP2 levels were positively correla-ted with UACR,serum creatinine,blood urea nitrogen,and negatively correlated with eGFR(P<0.05).In-creased serum FABP1 and FABP2 levels were independent risk factors for DKD.The serum FABP1,FABP2 joint detection diagnosis efficiency was better than that of serum FABP1,FABP2 detection alone(Z=4.712,4.363,P=0.001,0.002).Conclusion The serum levels of FABP1 and FABP2 are increased in patients with DKD,and they are related to the degree of renal function damage,which are independent risk factors for the occurrence of DKD in patients with T2DM.The combined detection of FABP1 and FABP2 has a high diagnos-tic efficiency for the occurrence of DKD in patients with T2DM.
7.Study on the level of urinary AD7c-NTP and its related factors in schizophrenic patients with positive and negative symptoms
Nan ZHAO ; Yinxia WU ; Ting JIA ; Laiqi YANG ; Juan WU ; Haoyuan SU ; Wentao MA
Chinese Journal of Behavioral Medicine and Brain Science 2018;27(10):901-905
Objective To investigate the difference of Alzheimer-associated neuronal thread protein ( AD7c-NTP) level and related factors among different symptom types of schizophrenia. Methods The con-centrations of AD7c-NTP in urine of 30 patients with positive symptoms,46 patients with negative symptoms and 24 controls were detected by enzyme linked immunosorbent assay( ELISA) . Positive and negative symp-tom scale ( PANSS) was used to assess schizophrenia patients. The correlation analysis was conducted be-tween the urine AD7c-NTP and demographic factors. Results The level of AD7c-NTP in urine of patients with negative symptoms((0. 88±0. 93) ng /ml)was higher than that in the patients with positive symptoms ((0. 50±0. 22)ng/ml,P<0. 05). The level of AD7c-NTP of in urine female patients((1. 16±1. 12)ng/ml) was higher than that in the male patients((0. 57± 0. 49)ng/ml,P<0. 01). AD7c-NTP levels in patients with a course of disease of more than 100 months((0. 96±0. 96)ng/ml) were higher than those in patients with a course of disease of less than 100 months((0. 60±0. 59)ng/ml,P<0. 05). The level of AD7c-NTP in pa-tients over 35 years old((0. 94±0. 96)ng/ml) were higher than that in patients under 35 years old((0. 62±0. 62)ng/ml,P<0. 05). The level of AD7c-NTP in patients with MMSE score of 0-22 points((0. 92±0. 80) ng/ml) were higher than that in patients with score of 23-29 points((0. 62±0. 74)ng/ml,P<0. 05). Before admission(at least 2 months),the level of AD7c-NTP in patients without persisting in taking drugs((0. 99± 0.95)ng/ml) was higher than that in patients with persisting in taking drugs((0. 62±0. 65)ng/ml,P<0. 05). The level of AD7c-NTP in schizophrenic patients was positively correlated with age and course of dis-ease( r=0. 29,0. 26,P<0. 05) ,and negatively correlated with smoking history and mini-mental state exami-nation( MMSE) ( r=-0. 13,-2. 41,P<0. 05) . Conclusion There is a difference in AD7c-NTP levels be-tween patients with positive and negative symptoms of schizophrenia. Gender,age,course of disease and anti-psychotics are important factors that affect AD7c-NTP levels in patients with schizophrenia.
8.Diagnosis value of PCT in patients with liver cirrhoses complicating spontaneous bacterial peritonitis analyzed by ROC curve
Xuezhen WU ; Yongliang WANG ; Haoyuan LUO ; Lu LIU
International Journal of Laboratory Medicine 2016;37(14):1928-1929,1932
Objective To evaluate the value of serum procalcitonin (PCT ) in the diagnosis of liver cirrhosis complicating sponta‐neous bacterial peritonitis (SBP) .Methods The patients with cirrhosis were divided into non‐SBP group and complicating SBP group according to whether complicating SBP ,and the patients with common hepatitis served as the control group .Serum expres‐sion levels of PCT ,CRP and IL‐6 were detected by electrocheniluminescence and Immunoturbidimetry methods .The receiver operat‐ing characteristic curve (ROC) curve was drawn for evaluating the diagnostic efficiency of each indicator .Results The levels of ser‐um PCT ,CRP and IL‐6 in the complicating SBP group were significantly higher than those in the non‐SBP group and control group , the differences were statistically significant (P<0 .01);The ROC curve analysis showed that the diagnostic value of PCT at the op‐timum threshold value of 0 .51 ng/mL for diagnosing cirrhosis complicating SBP was superior to CRP and IL‐6 ,the sensitivity of se‐rum PCT for diagnosing SBP in 3 groups was 62 .68% ,the specificity was 76 .59% and the accuracy was 80 .01% .Conclusion The serum PCT level has an important value for the early diagnosis of liver cirrhosis complicating SBP .

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