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71.
ZHU JINGDE 《Cell research》1995,(1)
INTanDUCTI0NMyeloidcelldifferentiati0n,inwhichmultip0tentialprogenitorcellsarec0nvertedint00neofthesixmaturedifferentiatedcells,i.e.,erythr0cytes,platelets(megakary-ocytes),macr0phages,neutr0phils,e0sinophilsandbas0phils,involvestemporalre-gulati0nofexpression0fanumberoflineage-anddifferentiationstage-specificgenes.Understandingthedevel0pmentalspecificationoflineageaJswellasmaturationstageassociatedpatterns0fgeneexpressioninmyel0idcelldifferentiationrequiresanin-sightintothecontrol0findivid… 相似文献
72.
INTRODUCTI0NThedifferentiati0nofcelIsalongthemonocyte-macr0phagepathwayandthesig-nalsinvo1vedinthesecel1sacquiringtheabilitytokilltum0rcellsarenotfllllyundersto0d.Wehavebeenstudingamoleculewhichappearst0beanimportantmemberofthecytokinenetworkinvo1vedintheregulati0nmonocyteactivation.ThiscytokinetermedP48wasisolatedfr0mthehllmannullcellleukemiacell1ineReh.IthasbeenpurifiedtohomogeneityandfOundtobedistinctfrominterferongamma,col0nystimulatingfactors(CSFs)andTNFalphaalldbeta[1,2].Func-ti… 相似文献
73.
浒苔多糖剂量150mg/kg可使高胆固醇血症小鼠血清胆固醇下降22%,剂量168mg/kg可使高脂血症大鼠TCH和TG分别降低58%和61%,HDL升高27%,剂量250mg/kg可分别提高血清、脑和肝SOD活力33%、118%和224%,剂量168mg/kg对高血脂大鼠血清和心脏LPO含量降低35%和46%。 相似文献
74.
Mouse egg activation, which includes release from meiotic metaphase II arrest, results from fertilization-induced increase in intracellular calcium concentration ([Ca2+]i). However, during egg activation caused by exposure to the protein synthesis inhibitor, cycloheximide, [Ca2+]i did not change. Although eggs fertilized in the presence of microtubule inhibitors remain arrested at metaphase, eggs treated for 32 hr with cycloheximide and the microtubule inhibitor, colcemid, formed nuclei. In untreated eggs aged in culture for 24 hr, the microtubule spindles became deformed. These eggs formed nuclei after exposure to cycloheximide, but not the calcium ionophore A23187. Our results indicate that eggs in which protein synthesis is inhibited are released from metaphase without an increase in [Ca2+]i, and despite disruption of the Spindle. © 1995 Wiley-Liss, Inc. 相似文献
75.
Na2SO3对热-DTT活化的游离CF1及类囊体膜上CF1-ATPase活力均有显著的促进作用,NaHCO3亦有明显的促进作用。Na2SO3和NaHCO3的促进作用与它们解除Mg2+的抑制作用有关。从NaHCO3和Na2SO3及它们与Mg2+之间的竞争性关系,表明三者是结合在酶的同一部位上。Na2SO3可明显降低热-DTT活化的游禹CF1-ATPase催化反应的活化能,这可能与促进产物ADP的释放有关。 相似文献
76.
Hamilton D Goodwin J Clarke MB du Moulin GC Liu V Caplan B Babbitt B 《Biotechnology and bioengineering》1994,43(8):700-705
An in vitro assay that measures the activation level of ex vivo activated (EVA) T cells currently being used in the adoptive immunotherapy of metastatic renal cell carcinoma has been developed. This assay is based on the ability of activated, but not resting. T cells to proliferate in response to the protein kinase C activator, phorbol myristate (PMA). To utilize this assay for in-process monitoring and control, we have begun an initial validation of the overall reproducibility of this assay. The proliferation of activated T cells in response to PMA, as measured by the mean cpm values of (3)H-thymidine incorporated, was demonstrated to have intra-assay coefficients of variation (cv's) for individual analysts that were typically less than 10% and rarely exceeded 20%. Activated T cells could be frozen and stored for at least 6 weeks with little or no deterioration in their ability to proliferate in response to PMA. Using these cells, inter-assay cv's that were typically less than 15% were obtained by individual analysts, and overall cv's of 10% to 25% were obtained for different samples assayed by different analysts at different times. This level of variability is very reasonable for a cellular assay. Furhter validation of this assay will address the issues of sensitivity, linearity and selectivity. To date, this assay has been used to analyze over 90 patient EVA cell samples and has revealed a broad range of proliferative responses to PMA. Taken together, these results suggest that this assay may be useful in defining the potency of the activated T cell used therapeutically. 相似文献
77.
After considering the need for quality control in NAA, the concept of quality in NAA procedures themselves is discussed, and
some important factors identified. Two approaches to improve quality are then described in more detail. The first concerns
the unique ability of NAA using different isotopic reactions and different modes (INAA/RNAA) to provide independent data sets
in the same laboratory, thus allowing internal validation or crosschecking. The second discusses the need for chemical yield
measurements in RNAA and the advantages of the radioisotopic tracer technique. Some recent advances and further possibilities
for this use of tracers are listed. 相似文献
78.
79.
Neutron-induced γ-ray emission tomography for quantitative determination of the concentration and distribution of elements
in a selected plane through a biological specimen is briefly explained and applied by way of illustration to the analysis
of gallstones. A system capable of carrying out studies of the binding site of75Se in different matrices using time differential perturbed angular correlation spectroscopy is also briefly described. Developments
in the detector technology of positron emission tomography have allowed small-diameter imaging devices to be built for in
vivo preclinical evaluation of new tracers in small animals and are discussed in the context of a proposed experiment combining
the techniques mentioned above. 相似文献
80.
P. Grochulski Y. Li J. D. Schrag M. Cygler 《Protein science : a publication of the Protein Society》1994,3(1):82-91
The structure of Candida rugosa lipase in a new crystal form has been determined and refined at 2.1 A resolution. The lipase molecule was found in an inactive conformation, with the active site shielded from the solvent by a part of the polypeptide chain-the flap. Comparison of this structure with the previously determined "open" form of this lipase, in which the active site is accessible to the solvent and presumably the substrate, shows that the transition between these 2 states requires only movement of the flap. The backbone NH groups forming the putative oxyanion hole do not change position during this rearrangement, indicating that this feature is preformed in the inactive state. The 2 lipase conformations probably correspond to states at opposite ends of the pathway of interfacial activation. Quantitative analysis indicates a large increase of the hydrophobic surface in the vicinity of the active site. The flap undergoes a flexible rearrangement during which some of its secondary structure refolds. The interactions of the flap with the rest of the protein change from mostly hydrophobic in the inactive form to largely hydrophilic in the "open" conformation. Although the flap movement cannot be described as a rigid body motion, it has very definite hinge points at Glu 66 and at Pro 92. The rearrangement is accompanied by a cis-trans isomerization of this proline, which likely increases the energy required for the transition between the 2 states, and may play a role in the stabilization of the active conformation at the water/lipid interface. Carbohydrate attached at Asn 351 also provides stabilization for the open conformation of the flap. 相似文献