Effects of diosmin on changes of TNF-α, IL-1β, IL-6, IL-8 and IL-10 in serum and kidney tissues of rats with kidney ischemia and reperfusion

AIM: To observe the effects of diosmin on the production of tumor necrosis factor-α(TNF-α), interleukin-1β(IL-1β), IL-6, IL-8 and IL-10 in serum and kidney tissues of rats with kidney ischemia and reperfusion (I/R). METHODS: Sprague-Dawley rats (180 in total) were randomly divided into 3 groups including sham operation group (sham),I/R group and diosmin+I/R group (diosmin+I/R). At the end of the experiment, the blood and kidney tissues were obtained and TNF-α, IL-1β, IL-6, IL-8 and IL-10 were detected by ELISA. RESULTS: The levels of TNF-α, IL-1β, IL-6, IL-8 and IL-10 in serum and kidney tissues in I/R group and diosmin+I/R group were significantly higher than those in sham group (P<0.01 or P<0.05). Following the development of the pathologic process, the level of TNF-α, IL-1β, IL-6 and IL-8 was significantly increased in I/R group and diosmin+I/R groups, but the level of IL-10 was significantly decreased in I/R group and significantly increased in diosmin+I/R group. The levels of TNF-α, IL-1β, IL-6 and IL-8 in I/R group was significantly higher than those in diosmin+I/R group (except TNF-α at 1 h in diosmin+I/R group). The level of IL-10 in diosmin+I/R group was significantly higher than that in I/R group (P<0.01 or P<0.05). CONCLUSION: Diosmin not only decreases the production of TNF-α, IL-1β, IL-6 and IL-8, but also promotes the production of anti-inflammatory cytokine IL-10, suggesting that the protective effect of diosmin on kidney I/R injury was associated with anti-inflammatory mechanism.     

Effect of S-nitrosylation induced by IL-1β and IFN-γ on DNA binding activity of cAMP response element binding protein in fibroblast-like synoviocytes

AIM: To investigate the effect of S-nitrosylation induced by recombinant interleukin-1β (rIL-1β) and recombinant interferon-γ (rIFN- γ) on DNA binding activity of cAMP response element binding protein (CREB) in fibroblast-like synoviocytes (FLSs). METHODS: (1)FLSs were incubated with rIL-1β and rIFN-γ in the presence or absence of inducible nitric oxide synthase inhibitor aminoguanidine (AG) for 12 h. The supernatant of the cell culture was collected to determine the contents of nitric oxide (NO). The total proteins prepared from each group ［only the total proteins prepared from rIL-1β+rIFN-γ group was reacted with dithiothreitol (DTT) for 15 min in vitro］ were subjected to the biotin switch assay, and the level of S-nitrosylation was determined by Western blotting. (2)FLSs were incubated with rIL-1β, rIL-1β+ rIFN-γ and AG respectively for 12 h. The nuclear extracts from each group were prepared. The nuclear extracts from each group were subjected to electrophoresis mobility shift assay to analyze the DNA binding activity of CREB (only the nuclear extracts from rIL-1β +rIFN-γ group was reacted with DTT for 15 min in vitro before assaying). RESULTS: rIL-1β plus rIFN-γ increased the production of NO and the level of S-nitrosylation, which was inhibited by AG. Administration of DTT in the total proteins reversed the induction of S-nitrosylation by rIL-1β and rIFN-γ. Co-incubation with rIL-1β and rIFN-γ inhibited the CREB activity induced by rIL-1β alone, which was reversed by AG. Administration of DTT in the nuclear extracts reversed the effect of co-incubation of the cytokines. CONCLUSION: Co-incubation with rIL-1β and rIFN-γ may increase the level of S-nitrosylation through inducing the production of endogenous NO, leading to reversible thiols modification of CREB and inhibit the DNA binding activity of CREB in FLSs.     

TL1A promotes development of intestinal fibrosis associated with chron?ic experimental colitis by regulating IL-17 and IFN-γ

AIM To explore how tumor recrosis factor ligand-related molecule 1A (TL1A) promotes the development of intestinal fibrosis associated with chronic experimental colitis by regulating interleukin-17 (IL-17) and interferon-γ (IFN-γ). METHODS Aexperimental colitis-associated wild-type (WT) and TL1A (L-Tg) transgenic intestinal fibrosis model was established by dextran sulfate sodium (DSS) induction.The severity of colitis was evaluated by detecting the disease activity index (DAI). HE staining was used to observe the histopathological changes and pathological score of the colitis.Myeloperoxidase (MPO) was measured in each group. The collagen deposition was detected by Masson’s trichrome staining and Sirius red staining. The lamina propria, spleen and mesenteric lymph nodes(MLN) mononuclear cells were isolated and counted, and the levels of IL-17 and IFN-γ weremeasured by ELISA, andthe percentages of CD4⁺IFN-γ⁺T cells and CD4⁺IL-17⁺T cells were analyzed by flow cytometry. RESULTS After drinking DSS water,the body weight of the mice in DSS/Tg group was decreased significantly as compared with WT group(P<0.05). The DAI score, histology score and MPO activity were significantly increased(P<0.05). Thelevels of IL-17 and IFN-γ, LPMC, spleen and MLN were significantly increased. The percentages of CD4⁺IFN-γ⁺T cells and CD4⁺IL-17⁺T cells were significantlyincreased.The thickness and collagen deposition of the colon were increased inTg group. CONCLUSION TL1A promotes the development of intestinal fibrosis associated with chronic experimental colitis by regulating IL-17 and IFN-γ.     

Effect of the acupotome therapy and electro-acupuncture on the serum contents of IL-1β, IL-6 and TNF-α in rabbits with knee osteoarthritis

AIM: IL-1β, IL-6 and TNF-α play important roles in emergence of osteoarthritis. This study aims at observing the effect of the acupotome therapy and electro-acupuncture on the cytokines in serum of rabbits with osteoarthritis. METHODS: 52 New Zealand rabbits were divided randomly into the normal group, model group, acupotome group and electro-acupuncture group. Knee osteoarthritis of the model rabbits was made with the straightened immobilization method. The acupotome and electro-acupuncture therapies were applied for three weeks. One week after the treatment the serum was collected, and the changes of IL-1β, IL-6 and TNF-α in serum were detected with RIA. RESULTS: In comparison with the control group, the contents of IL-1β, IL-6 and TNF-α elevated significantly in the knee osteoarthritis model group (P<0.05). Compared to the knee osteoarthritis model group, the contents of the cytokines in acupotome treatment group and electro-acupuncture treatment group decreased significantly (P<0.05). No significant difference between the content of cytokines in the acupotome treatment or electro-acupuncture treatment groups (P<0.05) was observed, also no statistical difference between the acupotome treatment or electro-cupuncture treatment groups and the control group was found. However, the contents of the three cytokines in the acupotome treatment and electro-acupuncture treatment groups were still higher than those in control group. CONCLUSION: The acupotome and electro-acupuncture treatment can decrease the release of IL-1β, IL-6 and TNF-α, indicating that the two therapies play an important role in improvement of the articular cartilage cell injury and function through inhibiting the generation of matrix protease and alleviation of degradation of the cartilage matrix.     

Association of single nucleotide polymorphisms of IL-1, IL-10 and TNF-β with rheumatoid arthritis in Chinese Han population from Quanzhou

AIM: To explore the genetic characteristics of enrolled rheumatoid arthritis and genetic mechanisms of rheumatoid arthritis (RA) by studying the associations of single nucleotide polymorphisms (SNPs) with rheumatoid arthritis in Chinese Han population from a very high prevalence area of rheumatoid arthritis, Quanzhou. METHODS: A case-control study of 155 rheumatoid arthritis patients (RA group) and 170 normal controls (control group) from Quanzhou were enrolled. All of 5 SNPs were genotyped by allele-specific polymerase chain reaction (PCR) and analyzed by SPSS 19.0. χ²-test was applied to predict Hardy-Weinberg equilibrium, and allele and genotype frequencies between RA group and control group were compared. Logistic regression models were used to analyze SNPs. Link disequilibrium analysis and haplotype analysis were performed with SHEsis software. RESULTS: Total of 1 SNP in control group was confirmed by Hardy-Weinberg equilibrium test (P>0.05), and 1 SNP in RA group was confirmed by Hardy-Weinberg equilibrium test (P>0.05). Allele frequencies of 4 SNPs were significantly different between control group and RA group (P <0.05). CONCLUSION: The SNPs of IL-10 rs1800893, IL-1β rs16944, TNF-β rs2009658 and TNF-β rs1041981 were associated with the incidence of rheumatoid arthritis in Chinese Han population of Quanzhou. Allele G of IL-10 rs1800893, allele G of IL-1β rs16944, allele C of TNF-β rs2009658 and allele C of TNF-β rs1041981 can be used as potential genetic markers for the diagnosis of RA in Quanzhou, Fujian.     

Effects of IFN-α 2b on telomerase activity and the toxic effects to cultured choroidal melanoma of human eyes

AIM:To study the effects of interferon-α 2b(IFN-α 2b) on the telomerase activity of choroidal melanoma cells of human eyes and the toxic effects to the cells.METHODS:IFN-α 2b was used with different concentrations and times to act on the primary cultured choroidal melanoma cells of human eyes. The toxic effects were evaluated by MTT assay and the levels of telomera activity were detected by PCR-ELISA assay. A correlation between the two results was analyzed.RESULTS:The telomerase activity gradually decreased following the increasing concentrations and times of treatment with IFN-α 2b, which accompany the step-up of restrain rate of the cells. At the point when the concentration attained 5×104 IU/L or the time attained 24 h, the telomerase activity decreased very obviously. However, the appearance of cell death lagged behind the decreasing of telomerase.CONCLUSION: IFN-α 2b is an effective telomerase inhibitor, which can decrease the telomerase activity in choroidal melanoma cells of human eyes effectively. The IFN-α 2b treatment is concentration and time dependent, and can cause the death of cultured cells.     

Expression and significance of TLR4 in Sombatis cell-based model of epilepsy

AIM：To study the change of Toll-like reporter 4 (TLR4) expression in Sombatis cell-based model of epilepsy and to explore the role of TLR4 in this model. METHODS：After cultured in vitro for 9 d, the neurons of newborn SD rats were randomly divided into control group and model group. The neurons in model group were cultured in low-magnesium medium for 3 h and then returned to the normal medium culture. The expression of TLR4 at mRNA and protein levels was detected by fluorescence quantitative PCR and the method of immunohistochemistry, respectively. RESULTS：The immunohistochemical results showed that the protein expression of TLR4 was enhanced in the Sombati’s cells. The results of fluorescence quantitative PCR showed that the mRNA expression of TLR4 time-dependently increased in the Sombatis cells (P<0.05). CONCLUSION：The expression of TLR4 in the neurons is up-regulated in Sombatis cell-based model of epilepsy in rats, suggesting that TLR4 is associated with the pathogenesis of epilepsy.     

Influence of IFN-γ combined with M-pred on human embryonic lung fibroblasts

AIM: To look for a better method to deal with interstitial lung disease, interferon-gamma (IFN-γ) combined with methylprednisolone (M-pred) to influence human embryonic lung fibroblast on proliferation, collagen synthesis and the expression of transforming growth factor-β1 (TGF-β1) protein and mRNA were investigated. METHODS: Exponentially growing cells were preincubated for 48 h before harvested. The microculture tetrazolium (MTT) assay was used to measure the inhibition ratios of M-pred combined with different concentrations of IFN-γ. The expression of proliferation cell nuclear antigen (PCNA) was detected by immunocytochemical analysis. Hydroxyproline kit was adopted to detect collagen synthesis. The expressions of TGF-β1 mRNA and protein were detected respectively by RT-PCR and Western blotting. RESULTS: Methylprednisolone, IFN-γ as well as the combination of methylprednisolone and IFN-γ inhibited the proliferation of HELF and the expression of PCNA in comparison with control group (P<0.05). That also decreased the expression of hydroxyproline, inhibited the expression of TGF-β1 mRNA and protein (P<0.05). The effectiveness of IFN-γ became stronger when the concentration increased. The synergistic effect between IFN-γ and methylprednisolone was observed (P<0.05). CONCLUSION: The combination effect of IFN-γ and methylprednisolone is augmented compared with using IFN-γ or methylprednisolone alone, suggesting that the combination use of both drugs has better anti-fibrous degeneration effect than use either alone.     

Effect of interfering TGF-β receptor Ⅱ expression on viability,differentiation and apoptosis of NB4 cells

AIM: To evaluate the effect of interfering TGF-β receptor Ⅱ (TβRⅡ) expression on the viability and differentiation of human acute promyelocytic leukemia NB4 cells induced by all-trans retinoic acid (ATRA) and their apoptosis induced by arsenic trioxide (ATO). METHODS: The technique of lentivirus-mediated RNA interference was used to obtain stable NB4 cells with TβRⅡ knockdown, named TβRⅡ-shRNA NB4 cells. CCK-8 assay was used to detect the viability of TβRⅡ-shRNA NB4 cells. The expression level of CD11b was analyzed by flow cytometry, and Wright-Giemsa staining was used to detect the effects of ATRA on the differentiation of TβRⅡ-shRNA NB4 cells. Double staining (Annexin V-FITC/PI) and AO/EB staining were used to detect the effects of ATO on the apoptosis of TβRⅡ-shRNA NB4 cells. RESULTS: The viability of TβRⅡ-shRNA NB4 cells was significantly higher than that of NB4 parental cells. The differentiation was induced in TβRⅡ-shRNA NB4 cells and NB4 parent cells by treatment with ATRA at different concentration (0.01, 0.02, 0.04, 0.08, 0.1 μmol/L) for 96 h. The differentiation rate of TβRⅡ-shRNA NB4 cells was lower than that of NB4 parental cells in a dose-dependent manner. ATO induced apoptosis of TβRⅡ-shRNA NB4 cells and NB4 parent cells at different concentrations (2, 4 and 8 μmol/L) for 24 h. The apoptotic rate of TβRⅡ-shRNA NB4 cells was lower than that of NB4 parental cells dose-dependently. At the concentration of 8 μmol/L for 24 h, the apoptotic rates in TβRⅡ-shRNA NB4 cells and NB4 cells were (49.15±2.05)% and (66.85±2.41)%, respectively (P<0.01). CONCLUSION: Down-regulation of TβRⅡ increases the viability of NB4 cells, inhibits NB4 cell differentiation induced by ATRA, and also inhibits apoptosis induced by ATO.     

A study on the mechanism of doxorubicin promoting IL-1β and collagen type I secretion in cardiac fibroblasts

AIM To observe the effect of adriamycin/doxorubicin （DOX） on the production of inflammatory cytokines and collagen in cardiac fibroblasts and its mechanism. METHODS Neonatal SD rat cardiac fibroblasts were isolated, cultured, and identified by immunofluorescence staining with monoclonal antibodies against vimentin observed under a confocal laser-scanning microscope. The Cell Counting Kit-8 assay was used to detect the toxicity of DOX on cardiac fibroblasts, and flow cytometry with annexin V-FITC/PI double staining was used to detect apoptosis. ELISA was used to detect the release of inflammatory factors in the supernatant of cultured cells. Immunofluorescence labeling assay was used to detected α-smooth muscle actin （α-SMA） expression and mitochondrial reactive oxygen species （mROS） in the cells. Western blot was used to detect the expression of nucleotide-binding oligomerization domain-like receptor protein 3 （NLRP3） inflammasome-related proteins in cardiac fibroblasts. RESULTS （1） Compared with the control group, DOX inhibited the proliferation of cardiac fibroblasts （P<0.05）, but had no significant effect on apoptosis （P>0.05）. （2） Treatment with DOX promotes the release of proinflammatory factors interleukin-1β （IL-1β） and IL-6 in cardiac fibroblasts （P<0.05）. （3） The expression of α-SMA, collagen type I and transforming growth factor-β in DOX treatment group increased significantly compared with control group （P<0.05）. （4） Compared with the control group, the levels of mROS, cellular NLRP3 and cleaved caspase-1 in cardiac fibroblasts increased significantly after DOX treatment. CONCLUSION Doxorubicin promotes cardiac fibroblasts to secrete IL-1β and collagen type I by promoting mROS production and activating NLRP3 inflammasome.     

Effects of immune-activated platelets and LDL on expression and activity of COX-2 and PPAR-α in HUVECs

AIM: To observe the effect of immune-activated platelets and low-density lipoprotein cholesterol (LDL) on the expression and activity of cyclooxygenase-2 (COX-2) and peroxisome proliferator activated receptor α (PPAR-α) in human umbilical vein endothelial cells (HUVECs) treated with activated platelets and LDL. METHODS: The platelets were activated by ADP. The co-culture system of HUVECs with immune activated platelets and/or LDL were established. The activity of COX-2 and expression of PPAR-α at mRNA and protein levels in HUVECs were detected by RT-PCR and Western blotting. The concentration of PGE2 was measured by ELISA for representing the COX-2 activity. The PPAR-α activity was determined by a nuclear factor assay kit. RESULTS: The COX-2 activity and mRNA expression of PPAR-α, the protein levels of COX-2 and PPAR-α and PGE2 concentration in activated platelets group were significant higher than those in un-activated platelets group (all P<0.01). No difference of PPAR-α binding activity was observed between two groups. LDL didnt affect the COX-2 activity and PPAR-α expression, but significantly promoted the stimulating effect of immune-activated platelets. CONCLUSION: Immune-activated platelets significantly promote COX-2 activity and PPAR-α expression in HUVECs, but dont change the PPAR-α binding activity. LDL at general concentration does not affect the expression and activity of COX-2 and PPAR-α, but promote the effect of activated platelets on HUVECs.     

The 4^th Meeting of East Asian and 10＋3 for Collaboration on Edible Fungi

November 3 ~6 ,2006Shanghai and Nantong,P.R.ChinaOrganized by MushroomBranch of the China Agricultural SocietyJapanese Society for MushroomScience and BiotechnologyThe Korean Society of MushroomScienceInstitute of Edible Fungi ,Shanghai Academy of Agricultural SciencesCo-organized by Jiangsu Alphay Bio-tech Co.,LtdShanghai Society for MicrobiologyShanghai Society for Horticultural ScienceTIMETABLE OF ACTIVITIESFRIDAY,3rdNovember ,20061400-1900 Registration (Foyer , …     

Divergent functions of SNAC4–9 and possible mechanisms for tomato adaptation to abiotic stresses

Plants are exposed to all types of abiotic stresses during the process of growth and development, which could adversely affect the productivity and postharvest storage quality of plants. In the current study, the expression of SNAC4–9 and the changes of physiological parameters were analyzed in tomato seedlings under various abiotic conditions and hormone treatments. The results demonstrate that all six genes were induced by these stresses at differential induction levels and that SNAC4–9 gene expression profiles were likely to be related to the ABA, SA, and MeJA signaling pathways. In addition, all of the stress- and hormone-treated seedlings exhibited significant increases in their proline content and antioxidant enzyme activities. MDA was significantly increased in seedlings exposed to stress and decreased in hormone-treated seedlings. These data collectively suggest that SNAC4–9 might function through ABA, SA, and JA signaling pathways and the regulation of proline and antioxidant systems. This study combines molecular biology and physiology to provide valuable information for further exploring the functional roles of NAC genes in response to environmental stresses and indicates that these genes may exhibit potential for enhancing stress tolerance of transgenic tomato plants and further improving the postharvest storage quality of tomato plants.     

TCRVβ7.1 transfection activates signal protein ERK and insreases IFN-γ expression in PBMCs

AIM: To investigate the effect of tumor-specific T cell receptor (TCR) gene transfection on production of cytokine and signaling activation in T cells.METHODS: TCRVβ7.1 gene was transferred into peripheral blood mononuclear cells (PBMCs) obtained from healthy adults, and the expression of Vβ7.1 was detected by flow cytometry before and after transfection. The total quantities of protein and phosphorylation of ERK1/2 were detected by Western blotting. The expressions of IL-4 and IFN-γ were detected by ELISA.RESULTS: The results of flow cytometry showed that TCRVβ7.1 protein was efficiently expressed after transfection. The phosphorylation level of ERK increased significantly in TCRVβ7.1-modified PBMCs, and was related with the activation of T cells. The expression of IFN-γ was significantly higher in TCR-transfected cells than that in non-transfected cells. The expression of IL-4, however, has no distinct difference between groups.CONCLUSION: The transfection of TCRVβ7.1 induces phosphorylation of ERK1/2 and production of IFN-γ, and activates T lymphocytes.     

Intervention of gossypol and relationship between cognitive function and expressions of 11β-HSD1 and GR in brain of type 2 diabetic rats

AIM: To study the effect of gossypol on the cognitive function of type 2 diabetic rats, and to explore its mechanism. METHODS: Thirty male Sprague-Dawley rats were divided into three groups randomly: normal group, type 2 diabetic group and gossypol treated group. After fed with high-fat diet for 4 weeks, the later two groups were injected with streptozotocin intraperitoneally to establish type 2 diabetic rat model. The animals in gossypol treated group were given gossypol at dosage of 15 mg/kg once per day for 4 weeks by gavage. Since 5th week, the times of gavages were changed into once per week at the same dosage and lasted to 12th week. Learning and memory abilities of rats were assayed with Morris water maze test. The concentration of blood glucose was measured by biochemical method. The levels of serum corticosterone and insulin were detected by enzyme-linked immunosorbent assay and radioimmunoassay, respectively. The protein expressions of 11β-HSD1 and GR in cerebral cortex and hippocampus were determined by Western blotting. The morphological changes of cerebral cortex and hippocampus were observed under light microscope and transmission electronic microscope, respectively. RESULTS: Compared to normal group, the karyopyknosis, dilation of golgiosome and mitochondria swelling of neuron from cerebral cortex and hippocampus were prominent in diabetic group. The concentrations of blood glucose, serum corticosterone and insulin increased significantly (P<0.01). Protein expression of GR decreased (P<0.05), 11β-HSD1 protein tended to increase. Platform searching score was lower (P<0.01) and escape latency was longer (P<0.01) in diabetic group. After treated with gossypol, the concentrations of blood glucose, serum corticosterone and insulin declined (P<0.01). The protein expression of 11β-HSD1 was decreased (P<0.05) and GR was increased (P<0.05). Escape latency was shorter (P<0.01) and platform searching score was increased (P<0.01). CONCLUSION: Gossypol may improve the cognitive function of type 2 diabetic rats. Decreasing the level of 11β-HSD1 and increasing GR protein in the brain may be involved in the mechanism.     

Effects of PPARα activation on AngⅡ-induced cardiomyocyte hypertrophy and interaction of NFATc4 with p65-NFκB

AIM：To investigate the effects of fenofibrate on angiotensin Ⅱ (AngⅡ)-induced cardiomyocyte hypertrophy. METHODS：Primary neonatal cardiomyocytes were pretreated with fenofibrate (10 μmol/L) for 1 h followed by stimulation with AngⅡ (100 nmol/L). The mRNA levels of ANF, BNP and β-MHC were measured by real-time PCR. Western blotting was employed to determine the nuclear translocations of NFATc4 and p65-NFκB. Co-immunoprecipitation was used to investigate the interaction of NFATc4 with p65-NFκB in the nucleus of cardiomyocytes. In addition, the DNA binding activity of NFATc4 on the BNP promoter was determined by EMSA. RESULTS：Fenofibrate significantly inhibited AngⅡ-induced cardiomyocyte hypertrophy. Fenofibrate treatment inhibited the nuclear translocations of NFATc4 and p65-NFκB, as well as the interactions of NFATc4 with p65-NFκB in the nucleus of cardiomyocytes induced by AngⅡ. Fenofibrate inhibited the binding activity of NFATc4 with the BNP promoter, which was strengthened by AngⅡ. CONCLUSION： Fenofibrate enhances the interaction of NFATc4 with PPARα, decreases the interaction of NFATc4 with p65-NFκB in the nucleus of cardiomyocytes, and inhibits the DNA binding activity of NFATc4 induced by AngⅡ, which may be the important mechanisms of fenofibrate on inhibiting cardiac hypertrophy.     

Effect of Pruning and Partial Disbudding on the Cropping of Comice and Beurré Hardy Pears

The effects of three intensities of pruning on fruit set, fruit bud development, cropping and vigour of intensively grown Cornice and Beurré Hardy pears were compared over a three-year period. Severe pruning, in which extension shoots were cut back to fruit buds on the two-year-old wood, greatly increased the set of fruits per 100 flower clusters and reduced vigour, in comparison with a renewal type of pruning. Severe pruning of Comice caused a relative reduction in the number of fruit buds in subsequent years, so the improvement in fruit set did not lead to an increase in crop per tree, but with Beurré Hardy fruit bud formation was unaffected and the crop per tree was increased by hard pruning. There was an improvement in yield in relation to tree size with both varieties. Pruning to fruit buds provides a means of increasing yields per acre by ‘containing’ pear trees at close spacings without reducing the yield per tree.

Partial disbudding just before blossoming increased fruit set but not enough to offset the reduction in number of fruit buds. Supplementary pollination did not improve the yields of Comice and increased the crop of Hardy in one year only.     

Analysis the efficiency of inter and intra-specific hybridization of new cultivars of sweet cherry and chinese cherry北大核心CSCD

【Objective】To explore the rules of intra-specional and inters-pecific cross breeding of some new sweet cherry cultivars and improve the efficiency of cross breeding of sweet cherry in the area where winter is warm and summer is hot and moist.【Methods】The intraspecial and interspecifichybridization test of sweet cherry was carried out by using sweet cherry as the mother,using sweet cherry and chinese cherry as the father. The rate of fruit set,embryo,embryo abort of the cross and quality of the F0 fruit were investigated in order to analysis the efficiency of the cross.【Results】The four cultivars of sweet cherry‘Jiangnanhong’‘Chaoyang-1’‘Changfeng-1’and‘Van’were taken as the mother. Five sweet cherry cultivars or selections‘04-8’‘04-11’‘Chaoyang-1’‘Van’‘Lapins’and five cultivars of chinese cherry‘Chaozaohong’‘Duanbing’‘Gejiawu’‘Heizhenzhu’‘Zijing’were taken as the male parent. Among them‘Jiangnanhong’and‘Zijing’are newly identified cultivars in Zhejiang province,and‘Chaoyang-1’and‘Changfeng-1’are new selections. After pollination for 1 week,the fruit setting rate was relatively high and significant decrease in the 4 weeks and mature stages in intra and inter- species with the development of fruits. In the mature stage,all the fruit setting of the other cross of intra-species were higher than 5%,except that of‘Jiangnanhong’ב04-11’was 1.85% lower than 3%,and that of‘Changfeng-1’בLapins’was 4.35% lower than 5%,which indicates the basic affinity between the cross of intra-specific sweet cherry. The fruit setting rate of intraspecific cross was higher than that of interspecific cross. The fruit setting rate of‘Chaoyang-1’was the highest in both intraspecific and interspecific hybridization. The interspecific hybrid combination of‘Changfeng-1’had the lowest fruiting rate. The embryo rate and abortion rate of the intraspecific cross were higher than those of interspecific cross when the female parent is same. The abortion rate is high when hybrid embryos mature,and only 4 crosses group can obtain non-abortion embryos,which are the hybrid cross of‘Jiangnanhong’with‘04-8’‘Lapins’‘Chaozaohong’,and the cross of‘Changfeng-1’with‘Van’. The abortion is lower when the hybrid embryos immature. The embryo rate was lowest and the abortion degree was the highest of the cross of‘Jiangnanghong’in immature embryo stage. The cross with the mother of‘Chaoyang-1’was the best with high setting rate,high embryo rate and low abortion rate in immature embryo stage,so‘Chaoyang-1’is the best female parent in this test.‘Chaoyang-1’and‘Zijing’were the better fathers in the ten test male parents for the cross with them had a high embryo rate (65.84% and 75.21%,respectively),and most of the embryos were bright white and full with good development in the immature embryos stage. ‘Chaoyang-1’is the best female and male parent in this test. The cross between‘Chaoyang-1’and‘Van’shows‘Chaoyang-1’is the better female than male parent. The ripening stage of F0 fruit was delayed,and the color and shape of F0 fruit showed the same col- or and shape of open pollination of parent fruit. The soluble solid of interspecific hybrid fruit was lower than that the intra-specific hybrid,and they all lower than that of the open pollinated female fruit. In order to obtain hybrid offspring,the author suggests three methods could be used in the area where is warm in winter,hot and moist in summer: one is selecting hybrid offspring which comes from the main producing areas,which means making cross and getting hybrid offspring in the main producing areas but select it in future planting area. The other is using embryos rescue technology after getting immature fruit; the third one is using mixed pollen for open pollination.【Conclusion】The fruit set and embryo development have significant differences among the different cross group in the area where winter is warm and summer is hot and moist. The fruit set is higher and the embryo abort is lower of intraspecific cross than that of interspecific cross when the mother is the same sweet cherry.‘Chaoyang-1’is the best female and male parent in this test when making cross. © 2019 Journal of Fruit Science