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981.
Damaged epithelia regenerated by bone marrow-derived cells in the human gastrointestinal tract 总被引:36,自引:0,他引:36
Okamoto R Yajima T Yamazaki M Kanai T Mukai M Okamoto S Ikeda Y Hibi T Inazawa J Watanabe M 《Nature medicine》2002,8(9):1011-1017
Studies have shown that bone marrow cells have the potential to differentiate into a variety of cell types. Here we show that bone marrow cells can repopulate the epithelia of the human gastrointestinal tract. Epithelial cells of male donor origin were distributed in every part of the gastrointestinal tract of female bone marrow transplant recipients. Donor-derived epithelial cells substantially repopulated the gastrointestinal tract during epithelial regeneration after graft-versus-host disease or ulcer formation. Regeneration of gastrointestinal epithelia with donor-derived cells in humans shows a potential clinical application of bone marrow-derived cells for repairing severely damaged epithelia, not only in the gastrointestinal tract but also in other tissues. 相似文献
982.
Mishima Y Terui Y Mishima Y Katsuyama M Mori M Tomizuka H Takizawa T Miyazato A Ueda M Yamada M Hayasawa H Mizunuma N Ishizaka Y Ikeda K Kato T Ozawa K Hatake K 《Journal of cellular physiology》2002,191(2):183-190
We have established a new hematopoietic cell line from a patient with myelodysplastic syndrome (MDS), which was refractory anemia with excess blasts (RAEB). This cell line, designated TER-3, depends on several cytokines for long-term survival and growth, and requires interleukin-3 (IL-3) for continuous growth. Cytochemical analysis revealed that TER-3 cells are weakly dianisidine positive and nonspecific esterase positive, but peroxidase negative. The surface marker profile shows that the TER-3 cells are strongly positive for myeloid, lymphoid, and megakaryocytic antigens such as CD15, CD19, and CD61, and negative for some common multilineage antigens such as CD13, CD33, and CD34. Thus, this cell line has a multilineage phenotype, suggesting that the transformation event occurred in multipotent stem cells. Dianisidine- and nonspecific esterase-positive TER-3 cells increase with granulocyte-colony stimulating factor (G-CSF) rather than with IL-3. These results suggest that the cell line is useful for understanding the mechanism underlying G-CSF-associated hematopoietic cell differentiation and activation in the patient with MDS. 相似文献
983.
984.
We have previously demonstrated that calcineurin and p38 mitogen-activated protein kinase (MAPK) are up-regulated in the hearts of mdx mice. However, the degree of up-regulation observed was variable, which may reflect variable levels of daily physical activities among the mice. To investigate whether or not exercise affects dystrophic features and activates intracellular signaling molecules in mdx hearts, we subjected mdx and C57BL/10 mice to treadmill exercise and examined intracellular signaling molecules in cardiac muscles, at the protein level. The heart to body weight ratio was significantly increased in exercised mdx mice. Histopathology in exercised mdx hearts showed extensive infiltration of inflammatory cells, together with increases in interstitial fibrosis and adipose tissues, all of which were not observed either in exercised C57BL/10 or non-exercised mdx hearts. Phosphorylated p38 MAPK, phosphorylated extracellular signal-regulated kinase 1/2 and calcineurin, but not phosphorylated c-Jun N-terminal kinase 1, were up-regulated in exercised mdx hearts compared to exercised C57BL/10 or non-exercised mdx hearts. These data suggest that physical exercise accelerates the dystrophic process through activation of intracellular signaling molecules in dystrophin-deficient hearts. 相似文献
985.
986.
Ikeda H Kikuchi K Noguchi J Takeda H Shimada A Mizokami T Kaneko H 《Theriogenology》2002,57(4):1309-1318
Preincubation of spermatozoa is important for capacitation and successful fertilization in vitro. The effects of preincubation time on frozen-thawed boar epididymal spermatozoa as measured by sperm motility, acrosomal integrity and fertilization ability in vitro were examined. Epididymal spermatozoa were collected from three Large White boars and frozen. The thawed spermatozoa were preincubated for 0, 15, 30, 60 and 120 min. Their motility was evaluated by a sperm motility analyzer and then the sperm motility indexes (SMIs) were calculated. The status of their acrosomal integrity was evaluated by triple-staining. Then, their fertilization ability was examined by in vitro fertilization (IVF) using porcine oocytes matured in vitro. SMIs of spermatozoa and the incidences of acrosome-intact live spermatozoa from the three boars were high (21-39 for SMI and 50-61% for acrosome-intact live spermatozoa) just after thawing, but both decreased as the duration of preincubation was prolonged (2-10 and 23-40%, respectively). The incidences of sperm penetration were high (61-89% of inseminated oocytes) when the sperm were preincubated for 0-60 min. However, sperm penetration decreased as the preincubation period was prolonged to 120 min. The degree of this decrease differed depending upon the boar from which the spermatozoa were obtained (10-72%). When the two parameters, sperm motility and acrosomal integrity, were analyzed statistically, the latter parameter rather than the former one showed a significant effect on penetration ability in vitro after each duration of preincubation. These results suggest that preincubation of frozen-thawed boar epididymal spermatozoa is not required for IVF and also that the maintenance of acrosomal integrity in unreacted status, rather than the maintenance of sperm motility, is important for fertilization ability after thawing and during preincubation of boar epididymal spermatozoa. 相似文献
987.
Ohashi S Kubo T Kishida T Ikeda T Takahashi K Arai Y Terauchi R Asada H Imanishi J Mazda O 《Biochemical and biophysical research communications》2002,293(5):1530-1535
This present study aims at establishing a novel in vivo gene delivery system for intra-articular tissues. Plasmid DNA (pDNA) carrying the firefly luciferase or enhanced green fluorescent protein (EGFP) genes as markers was injected into a joint space and electric stimuli were given percutaneously with a pair of electrodes. Injection with naked pDNA alone did not induce any detectable level of luciferase activity, whereas electroporation at 25-500 V/0.7 cm resulted in a significant expression of the marker gene in the synovium. The expression level depended on the voltage, the optimum transfection being achieved at 150 V/0.7 cm. When the Epstein-Barr virus (EBV)-based plasmid vectors harboring the EBV nuclear antigen 1 (EBNA1) gene and oriP sequence were substituted for conventional pDNA, the transfection efficiency was increased approximately 5-10 times. Histological examination of the EGFP gene-transfected joints revealed that the marker gene was expressed in the synovial membrane while other intra-articular tissues such as articular cartilage were negative for the transgene product. Transgene-specific mRNA was demonstrated in synovium but not in other organs as estimated by RT-PCR analysis. The present results strongly suggest that in vivo electroporation is a quite simple, safe, and effective gene delivery method that could be applicable to gene therapy against articular diseases. 相似文献
988.
Takashi Sugita Akemi Nishikawa Reiko Ikeda Takako Shinoda Hiroyuki Sakashita Youko Sakai Yasuyuki Yoshizawa 《Microbiology and immunology》1998,42(7):475-478
Trichosporon species have been known to cause summer-type hypersensitivity pneumonitis (SHP). During the isolation of yeasts from an SHP patient's house, we recovered a strain belonging to the genus Trichosporon. Morphologically, the isolate produced rectangular arthroconidia when grown on corn meal agar. DNA-DNA hybridization experiments identified the isolate as T. ovoides. A slide agglutination test using specific factor sera demonstrated that the serotype of the strain was type II. Previously, T. asahii, a serotype II species, was considered to be the major antigen of SHP, but it is possible that T. ovoides may also be responsible for SHP. This is the first report of T. ovoides isolated from an SHP patient's home environment. 相似文献
989.
990.
Abstract: The growth and reproduction of Japanese forbs ( Artemisia princeps and Piantago asiatica ) and grasses ( Digitaria ad-scendens and Eleusine indica ) treated to 25 tramplings (3 g m-2 ) per week were investigated in relation to the toughness (tensile strength) of organs. The perennial erect forb, A. princeps , was the most sensitive to trampling in terms of a remarkable depression of plant size and relative growth rate (RGR). RGR and net assimilation rate (NAR) of trampled A. princeps were negative. This was promoted by a loss of organs due to a reduced toughness of organs following trampling. In contrast to this species which did not flower after trampling, the perennial rosette forb, P. asiatica , maintained its plant biomass, NAR, RGR and reproduction under trampling because of tougher organs. However, NAR without trampling was lower in P. asiatica due to a larger leaf dry mass per leaf area (LMA), which could contribute to leaf toughness under trampling. The annual tussock grass, D. adscendens , which has a greater RGR than that of another grass, E. indica , without trampling was intolerant to trampling in terms of decreased biomass and RGR under trampling due to more sensitive organs, although it maintained an ability to reproduce. On the other hand, E. indica showed a marked trampling tolerance, with hardly reduced plant biomass and RGR. This species showed increased toughness of organs when trampled and frequently formed inflorescences in the growing period and produced similar biomass allocation to reproductive organs to untrarnpled plants. Between the grasses, RGR without trampling was slower in E. indica , partly because of its larger LMA. These results suggest that plants face a dilemma between trampling tolerance and efficient assimilative capacity and/or growth rate. 相似文献