In order to study whether there is a direct interaction between the key variant gene(AP-PV-YN-Mut)protein of atypical porcine pestivirus(APPV)Yunnan strain and the host protein signal sequence receptor subunit 4(SSR4),the physical and chemical properties,spatial structure and subcellular localization of SSR4 protein were analyzed and predicted using online software such as ProtParam,PredictProtein and TMHMM.The recombinant vectors pCMV-Tag4A-SSR4 and pET-GST-Mut were constructed for GST pull-down test in vitro.The recombinant vectors pBiFC-VN173-SSR4 and pBiFC-VC155-Mut were constructed and the bimolecular fluorescence comple-mentary test(BiFC)was performed in cells to verify whether there was direct interaction between APPV-YN-Mut and host protein SSR4 in vitro and in cells.The results showed that SSR4 protein was a hydrophobic stable protein with no transmembrane structure and signal peptide.The second-ary structure was mainly irregular curl,and the tertiary structure was stable,mainly located in the endoplasmic reticulum.GST pull-down and BiFC experiments showed that APPV-YN-Mut interac-ted directly with host protein SSR4 in vitro and in cells.

In order to study whether there is a direct interaction between the key variant gene(AP-PV-YN-Mut)protein of atypical porcine pestivirus(APPV)Yunnan strain and the host protein signal sequence receptor subunit 4(SSR4),the physical and chemical properties,spatial structure and subcellular localization of SSR4 protein were analyzed and predicted using online software such as ProtParam,PredictProtein and TMHMM.The recombinant vectors pCMV-Tag4A-SSR4 and pET-GST-Mut were constructed for GST pull-down test in vitro.The recombinant vectors pBiFC-VN173-SSR4 and pBiFC-VC155-Mut were constructed and the bimolecular fluorescence comple-mentary test(BiFC)was performed in cells to verify whether there was direct interaction between APPV-YN-Mut and host protein SSR4 in vitro and in cells.The results showed that SSR4 protein was a hydrophobic stable protein with no transmembrane structure and signal peptide.The second-ary structure was mainly irregular curl,and the tertiary structure was stable,mainly located in the endoplasmic reticulum.GST pull-down and BiFC experiments showed that APPV-YN-Mut interac-ted directly with host protein SSR4 in vitro and in cells.

Objective Based on the principle of uncemented stem design, the femoral anteversion in different CT planes before total hip arthroplasty (THA) and stem anteversion after THA was compared, so as to find out the preoperative measurement to estimate stem anteversion in patients with developmental dysplasia of the hip(DDH) after THA. Methods Twenty-one primary THA patients (28 hips) who were diagnosed with DDH between September 2007 and May 2013 in Shanghai Ninth People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine were selected. Preoperative and postoperative CT scans were performed on all patients. The femoral anteversion angle was defined as the angle between the midcortical line between the anterior and posterior cortical line in five CT slices and the posterior condylar axis. The slice levels for the 4 femoral sites were selected，including the area just distal to the femoral head, the center of the lesser trochanter，1 cm height above center of the lesser trochanter, 2 cm height above center of the lesser trochanter (marked as femoral anteversion 1-4). Femoral anteversion 5 was defined as the midcortical line of the anterior cortical line in the slice of 2 cm height above center of the lesser trochanter and the posterior cortical line in the slice of 50% of the distance from the top of greater trochanter to the center of the lesser trochanter above the center of the lesser trochanter. The stem anteversion angle was defined as the angle formed by the stem neck major axis and the posterior aspect of the femoral condylar line. The cup version and stem alignment were also calculated. The difference value and correlation coefficients of femoral anteversion 1-5 and stem anteversion were compared. Results Femoral anteversion 1-5 was 17.70°±10.54°, 35.59°±7.21°, 31.09°±7.98°, 24.71°±9.11°, 21.94°±10.10°, respectively。Stem anteversion was 20.52°±10.90°. The difference value between stem anteversion and femoral anteversion 1-5 was 2.82°±6.27°, -15.08°±7.99°, -13.80°±15.68°, -4.19°±5.69°, -1.42°±4.07°, respectively. Cup anteversion was 25.60°±11.65°, and combined antevertion was 46.11°±13.28°，sagittal stem tilt was 1.13°±1.53°. There were statistically significant differences between femoral anteversion 1-4 and stem anteversion (P＜0.05), and no statistical difference was found between femoral anteversion 5 and stem anteversion. The correlation coefficients of femoral anteversion 1-5 and stem anteversion were 0.829, 0.681, 0.689, 0.853, 0.928, respectively. Conclusions Femoral anteversion 5 had a highly positive correlation with stem anteversion, which was an effective a substitute of stem anteversion before THA.

OBJECTIVETo explore the diagnostic value of MRI and SPECT in early postburn brain edema in severely burned dogs.

METHODSTwenty-six mongrel dogs were randomized into control (n = 6) and burned groups in which every 5 dogs were allotted to each of following time points: 6, 12, 18 and 24 postburn hours (PBHs). The dogs in burn groups were inflicted with 50% TBSA of III degree skin burn and were infused with 5% glucose solution after 6 PBHs, so that severe early postburn brain edema was produced. MRI and SPECT were employed to observe dynamically the brain of dogs in all groups. The results were collected and compared with one another.

RESULTSThe results indicated that with MRI brain morphological change of early brain edema could be shown as early as within 12 PBH and diffuse brain edema became more obvious with elapse of time. The changes might be difficult to be found by MRI when T(1)WISIR decreased below 10%. T(2)WI SIR increased by 8.29% at 24 PBH with blurred demarcation between the brain gray and white matters. There was diffused and progressive nuclide ((99)TCm-ECD) concentration in the brain tissue as shown by SPECT at 6 PBH. The radio-nuclide taking ratio increased significantly after 12 PBH, especially at 24 PBH (P < 0.01) when compared with that before burn.

CONCLUSIONCombined application of MRI and SPECT could evidently increase sensitivity and specificity in the diagnosis of early postburn brain edema.

Animals ; Brain Edema ; diagnosis ; diagnostic imaging ; Burns ; complications ; Dogs ; Magnetic Resonance Imaging ; Male ; Tomography, Emission-Computed, Single-Photon

Objective: To investigate the correlation between MRI features and pathology in brain edema at the early stage of severe burn (50％ TBSA Ⅲ degree) in dogs.Methods: Fifty-two dogs were randomized into control, simple burn (SB), burn plus sodium lactate (BSL), and burn plus glucose solution groups (BGS). The manifestation of the brain of control group was compared with that of burn groups at 6, 12, 18 and 24 hours postburn with MRI and pathological examination (gross appearance, electron microscopy and light microscopy).Results: The earliest findings of brain edema were seen at 12 hours after burn in BGS group, in which brain swelling was the main feature of MRI. The decrease of SIR on T1WI was not observed until it was exceeded 10％.Signal of T2WI increased by 8.29％ at 24 hours after burn.It was difficult to distinguish the gray matter from the white matter at the boundary line, which became blurred later. Histological changes of brain edema were observed as early as 6 hours after burn, being accompanied by swelling of endothelial cells and peri-vescular astrocytes, and vacuolation took place in neurons at 12 hours after burn, with different degrees of necrosis of capillary endothelimn,neurons, and axons. These changes became more marked with elapse of time. The BGS group showed the most obvious changes mentioned above at 24 hours after burn.Conclusions: The model of the brain edema after severe burn has the feature of both vasogenic edema and cytotoxic edema on the MRI and pathology. Positive MRI findings lagged behind that of the pathomorphological changes.