[Teaching poetry in the school of nursing--for imagination training. 7].
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Biomedical subjects
Publications and source records attributed to Y Ohkubo.
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Sulfation of glycosaminoglycans and glycopeptides was compared in baby hamster kidney (BHK) cells and the polyoma virus transformants (PY-BHK). Cells were incubated with [3H]glucosamine and [35S]sulfate, and the labeled glycosaminoglycans and glycopeptides were isolated by digesting the cell membrane fraction with pronase followed by gel filtration. Each type of glycosaminoglycan in the void volume fraction (Fraction I) and in the included fraction (Fraction II) was determined by sequential enzymatic digestions. The residue was regarded as being glycopeptides. Of the total 3H radioactivities of glycosaminoglycans in Fraction I from BHK cells, 51% were in dermatan sulfate, 23% were in heparan sulfate, 17% were in chondroitin 4- and 6-sulfates, and 9% were in hyaluronate. PY-BHK cells acquired significantly larger amounts of 3H radioactivities in sulfated glycosaminoglycans than did BHK cells on the basis of cell number. On the basis of protein content, there was no such difference due to higher protein content of PY-BHK cells. The degree of sulfation of the glycosaminoglycans, estimated from the ratio of 35S to 3H and by disaccharide analysis, was significantly lower in PY-BHK cells than in BHK cells. Considerable amounts of 35S radioactivities assigned to sulfated glycopeptides were found in Fraction II from both BHK and PY-BHK cells.
Heparitinase [EC 4.2.2.8, heparitin sulfate lyase] was prepared from an extract of cultured cells of Flavobacterium heparinum. Purification of the enzyme was achieved by repeating the hydroxyapatite column chromatography. The enzyme was used to degrade heparan sulfate occurring on the surfaces of ascites hepatoma cells, AH 66. From the supernatant of the enzyme-treated cells, breakdown products from heparan sulfate could be detected by paper chromatography. The heparitinase was found to be more effective than trypsin in removing heparan sulfate from the cells. Furthermore, on analyzing glycosaminoglycans and glycopeptides from the enzyme-treated cells and control cells, it was concluded that heparan sulfate was exclusively present on the cell surface and accessible to the heparitinase whereas other cell surface complex carbohydrates remained intact.
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We describe a patient with chronic expanding hematoma that was pathologically confirmed by examination of the resected specimen. It has increased gradually in the right lower lung field during a period of 10 years without symptoms. The MR T2-weighted image was useful to establish a diagnosis of chronic expanding hematoma, because of the mosaic of various signal intensities we named the "mosaic sign".
Multiplanar reconstruction (MPR) is a method that allows free selection of computerized reconstruction images. We reviewed a total of six MPR magnetic resonance (MR) examinations in five cases of adenoid cystic carcinoma of the central airway, which is a rare low-grade malignant tumor. MPR MR provides images either longitudinally or at right angles to the longitudinal axis of the trachea and main bronchi, so it was useful to diagnose tumor extent along airways more precisely and to evaluate therapeutic effects. MPR MR may help in planning therapeutic strategy and in posttherapeutic follow-up.
Sixty-one CT scans in 20 patients who had undergone head and neck reconstructive surgery using a pectoralis major myocutaneous (PM-MC) flap were retrospectively evaluated to assess the usefulness of Ct in the follow-up of these patients. The normal CT findings in patients with PM-MC flaps are described. Of 13 cases with tumor recurrence, CT examination correctly detected recurrent masses in all cases, including 3 in which there was no clinical sign of recurrence. Postoperative masses mimicking tumor recurrence included deformed breast tissue, hematomas, lymphoceles, and abscesses. Computed tomography was of great value in the detection of tumor recurrence, but careful interpretation is required because a postoperative complication or anatomic alteration may lead to the erroneous diagnosis of tumor recurrence.
A 65-year-old man with 6 osseous metastatic lesions was successfully treated by nephrectomy. Five of 6 metastatic tumors, 2 of which were histologically proved, dramatically regressed and disappeared roentgenographically. The other metastasis was removed by amputation 4 years prior to the nephrectomy. No apparent complication was found after the nephrectomy and the patient is in very good health. The factors responsible for regression of osseous metastatic renal cell carcinoma cannot be fully explained. The only common treatment given to 4 patients whose osseous renal cell cancer regressed, was nephrectomy. Since every therapy for metastatic renal cell cancer is unreliable, palliative nephrectomy seems to be justified as a treatment of choice even when osseous metastases are noted and there is a possibility of regression of metastatic lesions. Regression of osseous metastasis from renal cell carcinoma is extremely rare and only 3 cases have been reported.
A labeled avidin-biotin enzyme-linked immunosorbent assay (LAB-ELISA) for detecting antibody to infectious laryngotracheitis (ILT) virus in chicken sera was developed and compared with ordinary ELISA. Purified ILT virus, biotin-labeled anti-chicken IgG rabbit IgG conjugate, and horseradish-peroxidase-labeled avidin were used in the LAB-ELISA. When sera from farm chickens were tested by serum neutralization (SN) and two kinds of ELISA, the correlation rate between SN and LAB-ELISA was 50/50 (100%), and that between SN and ordinary ELISA was 39/50 (78%). In LAB-ELISA, all of the sera that were antibody-negative by SN had low absorbance (A) values (below 0.05), and the A values were closely correlated with the SN indexes. In ordinary ELISA, however, the sera antibody-negative by SN had various A values ranging from 0.06 to 0.32. LAB-ELISA had much lower nonspecific reactions than ordinary ELISA against sera from ILT-negative chickens, even when chickens were 30 weeks old. ILT antibody production after ILT vaccination could be detected by LAB-ELISA. A values peaked 5 weeks postinoculation and were maintained for 17 weeks.