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71.
目的 比较观察双相接种法和静置接种法构建组织工程骨对种子细胞增殖、分化和成骨表达的影响。方法 取健康志愿者骨髓,密度梯度离心法分离骨髓间充质干细胞并进行体外扩增、诱导分化,然后应用双相接种法和静置接种法与脱钙骨基质(DBM)复合构建组织工程骨,体外培养3周,用倒置显微镜、扫描电镜观察细胞密度、形态及基质分泌情况,并在不同时相点测定组织块中DNA含量、碱性磷酸酶(ALP)活性及钙含量变化。结果 倒置显微镜下双相接种法构建的组织块可见大量具有一定折光性的梭形细胞存在于胶原基质中。扫描电镜见双相接种法构建的组织块切面较平坦,孔隙较小,细胞包埋在胶原中,而静置接种法构建的组织块可见细胞、细胞外基质较少。在体外培养过程中,双相接种法组织块中细胞的DNA含量、ALP活性均高于静置接种法,钙含量在培养2周后高于静置接种法。结论 双相接种法是一种高效的组织工程骨构建方法,有利于提高接种效率和促进组织工程骨的体外成熟。 相似文献
72.
73.
Elemental composition and water content of myelinated axons and glial cells in rat central nervous system 总被引:1,自引:0,他引:1
The distribution of elements (e.g. Na, Cl, K) and water in CNS cells is unknown. Therefore, electron probe X-ray microanalysis (EPMA) was used to measure water content and concentrations (mmol/kg dry or wet weight) of Na, Mg, P, S, Cl, K and Ca in morphological compartments of myelinated axons and glial cells from rat optic nerve and cervical spinal cord white matter. Axons in both CNS regions exhibited similar water content ( 90%), and relatively high concentrations (wet and dry weight) of K with low Na and Ca levels. The K content of axons was related to diameter, i.e. small axons in spinal cord and optic nerve had significantly less (25–50%) K than larger diameter axons from the same CNS region. The elemental composition of spinal cord mitochondria was similar to corresponding axoplasm, whereas the water content (75%) of these organelles was substantially lower than that of axoplasm. In glial cell cytoplasm of both CNS areas, P and K (wet and dry weight) were the most abundant elements and water content was approximately 75%. CNS myelin had predominantly high P levels and the lowest water content (33–55%) of any compartment measured. The results of this study demonstrate that each morphological compartment of CNS axons and glia exhibits a characteristic elemental composition and water content which might be related to the structure and function of that neuronal region. 相似文献
74.
自体表皮细胞培养与异体真皮组合应用研究 总被引:13,自引:0,他引:13
严重烧伤病人皮肤修复中主要未解决的问题是真皮的替代。动物实验结果表明,异体皮移植后5天,用自体培养表皮细胞膜片覆盖真皮床,14天后复合皮成活率是84.6%±2.4%。组织学检查证实表皮已形成了复层结构,可见基底层、颗粒层和角质层。临床应用中,异体皮移植后10天,去除异体表皮覆盖病人的自体培养表皮,35天后未见排斥征象,异体真皮促进了培养表皮的分层、成熟和完整,组织学检查证实表皮细胞的边缘清楚,已分化形成颗粒层和角质层,真皮多细胞,已血管化,但表皮嵴缺乏。 相似文献
75.
76.
采用模拟在人体中使用的实测超声剂量,对体外培养的L-929株细胞进行辐照,通过细胞回复能力试验,观察回复前后的细胞增殖与抑制。对体外培养的人胚肺纤维细胞经1次及5次辐照,观察了DNA及细胞核面积的影响。并通过电镜观察了细胞超微结构的变化。上述实验结果,均提示经辐照后细胞有增殖趋向 相似文献
77.
Macrophages, dendritic cells or B lymphocytes have been shownto play a major role in the presentation of soluble antigensto CD4+ T cells. In contrast, the capacity of these cells topresent particulate antigens such as bacterial or parasiticantigens to T cells remains controversial. To investigate thisquestion, well defined particulate antigens were prepared bycovalent linkage of proteins or peptides to 1 µm in diametersynthetic microspheres. The T cell immunogenicity of such particulateantigens was analyzed in vitro and in vivo. In vitro, a solubleprotein such as hen egg lysozyme (HEL) coupled to beads stimulateda strong proliferative T cell response of lymph node cells fromHEL-primed mice or of specific T cell hybridomas. HEL coupledto beads was presented to the specific T cell hybridomas bysplenocytes or by peritoneal macrophages, but not by lymphomaB cells. Immunization of mice with several different proteinantigens or with a synthetic peptide covalently linked to beadsinduced strong CD4+ T cell responses in the absence of adjuvant.The strong in vivo immunogenicity of proteins coupled to beadsdid not result from a non-specific adjuvant effect of beadssince covalent linkage of the antigen to beads was strictlyrequired to induce T cell responses in the absence of adjuvant.In vivo treatment by carrageenan showed that macrophages arerequired for the in vivo stimulation of T cell responses bythese particulate antigens. Thus, these results demonstratedthe role of phagocytic cells, especially macrophages, for invivo presentation of particulate antigens. These particulateantigens represent an interesting approach for the developmentof new vaccines, and for the in vivo analysis of the role ofvarious antigen presenting cells in T cell activation and differentiation. 相似文献
78.
The cellular and regional distribution of glutathione (GSH) and GSH-related enzyme systems involved in cellular defense against reactive oxygen species and electrophilic xenobiotics in the nervous system has been extensively studied. However, little is known about the subcellular distribution of GSH systems in brain tissue and cultured neural cells. The present study investigates the distribution of mitochondrial and cytosolic GSH and GSH-related enzymes in cultured cerebellar astrocytes and granule cells, and compares them with levels in the adult rat cerebellum. Cytosolic GSH levels and cytosolic activities of glutathione reductase (GR), glutathione peroxidase (GPx) and glutathione-S-transferase (GST) in astrocytes were 57, 153, 245, and 92% higher than those found in granule cells, respectively. In contrast, granule cells contained significantly higher mitochondrial GSH levels than astrocytes. Granule cells also demonstrated comparable mitochondria/cytosolic concentrations of GSH and GR, GPX and GST activities to those observed in the cerebellar tissue, whereas ratios in astrocytes were markedly lower. Although in vitro treatments with 100 μM ethacrynic acid depleted both cytosolic and mitochondrial GSH in cultured astrocytes and granule cells in a time-dependent fashion, cellular GSH in granule cells was more resistant to the GSH-depleting agent than astrocytes. These results suggest that although GSH and GSH-related enzymes are abundant in cytosolic compartments of astrocytes, mitochondrial pools are relatively small. Since brain mitochondria are sites of significant hydrogen peroxide generation, the mitochondrial localization of GSH and its associated enzymes in neural cells provide important defenses against toxic oxygen species in the nervous system. Differences in subcellular distribution of GSH systems in individual neural cell types may provide a basis for selective cellular and/or subcellular expression of neurotoxicity. 相似文献
79.
F. G. Toback M.D. Ph.D. S. Kartha M. M. Walsh-Reitz 《Journal of molecular medicine (Berlin, Germany)》1993,71(10):861-866
Conclusion The mechanisms that regulate regeneration of kidney epithelial cells after acute tubular necrosis are poorly understood. Repair of the nephron can take place in the adverse systemic metabolic setting caused by failure of renal function. This clinical observation suggests that factors released at the site of the tubular insult can mediate repair. Studies carried out in this and other laboratories show that kidney epithelial cells can release and respond to polypeptide growth factors which may thereby contribute to renal regeneration by autocrine and paracrine mechanisms. Specific growth factors secreted by cells and deposited in the tubular basement membrane prior to injury may subsequently participate in nephron repair. In addition, adenine nucleotides released from injured or dying cells at the injury site or provided exogenously could stimulate surviving renal epithelial cells at the edges of the wound to migrate along the basement membrane to rapidly reepithelialize the nephron and subsequently initiate mitogenesis to replace cells lost by necrosis.The nephrotoxic effect of many agents used in cancer chemotherapy and the older age of patients undergoing complicated surgical procedures has increased the incidence of ARF, whereas the mortality rate has not changed since the early 1950s [22]. Thus there is considerable need for innovative therapeutic strategies. An important goal of future research efforts is to identify new growth factors that facilitate migration, differentiation, and proliferation of renal epithelial cells at sites of tubular necrosis. Isolation and use of these agents in combination with dialysis and nutritional support could speed renal regeneration and thereby improve the outcome in patients with this condition.Abbreviations ARF
acute renal failure
- ECM
extracellular matrix
- EGF
epidermal growth factor
- FGF
fibroblast growth factor
- IGF
insulin-like growth factor
- MGSA
melanocyte growth-stimulating activity
- PDGF
platelet-derived growth factor
- IGF
transforming growth factor 相似文献
80.