نتایج جستجو برای: سلولهای p388d1

تعداد نتایج: 3379  

ژورنال: :فیض 0
مرتضی سلیمیان mortaza salimian faculty of paramedical science, kashan university of medical sciences, kashan, iranدانشگاه علوم پزشکی کاشان، دانشکده پیراپزشکی زهرا سهیلی zahra soheili بهرام گلیایی bahram goliaei

سابقه و هدف: تکنیک های هم کشت ( co-culture ) در مطالعه تاثیرات متقابل سلولها نقش مهمی دارند. قابلیت افتراق بین جمعیت های سلولی هم کشت شده در ارزیابی این نوع کشت نقش اساسی دارد. سلول های p388d1 از گروه سلول های شبه ماکروفاژی هستند ولی ظاهری شبیه لنفوبلاست دارند. در ارزیابی هم کشت سلول های p388d1 و سلول های مغز استخوان، تفاوت در آنتی ژن های سطحی این دو جمعیت سلولی می تواند به افتراق آنها کمک کند....

ژورنال: فیض 2005
سلیمیان, مرتضی, سهیلی, زهرا, گلیایی, بهرام,

سابقه و هدف: تکنیک‌های هم‌کشت ( co-culture ) در مطالعه تاثیرات متقابل سلولها نقش مهمی دارند. قابلیت افتراق بین جمعیت‌های سلولی هم‌کشت شده در ارزیابی این نوع کشت نقش اساسی دارد. سلول‌های P388D1 از گروه سلول‌های شبه ماکروفاژی هستند ولی ظاهری شبیه لنفوبلاست دارند. در ارزیابی هم‌کشت سلول‌های P388D1 و سلول‌های مغز استخوان، تفاوت در آنتی‌ژن‌های سطحی این دو جمعیت سلولی می‌تواند به افتراق آنها کمک کند....

Journal: :The Journal of biological chemistry 1993
S E Barbour E A Dennis

Macrophage-like P388D1 cells release [3H]arachidonic acid and produce prostaglandin E2 (PGE2) upon stimulation with bacterial lipopolysaccharide (LPS) and platelet-activating factor (PAF). To determine whether group II phospholipase A2 (PLA2) is involved in this release, we treated P388D1 cells with antisense inhibitors specific for group II PLA2 RNA. Treatment with oligonucleotide ASGII decrea...

Journal: :Infection and immunity 1993
J B Messick Y Rikihisa

The binding, internalization, and proliferation of Ehrlichia risticii in P388D1 cells and equine polymorphonuclear (PMN) leukocytes were studied by immunofluorescent staining and flow cytometric analysis. The binding of ehrlichiae to P388D1 cells at 4 degrees C was dose dependent, and the antigens of bound organisms were susceptible to pronase treatment. Additionally, the binding of ehrlichiae ...

Journal: :Cellular immunology 1985
K H Kim M J Solvay D W Thomas

In this report we examined the antigen-presenting cell (APC) requirements for activation of T-cell hybridomas specific for the protein antigen PPD (purified protein derivative of tuberculin). During the course of these studies we observed that glutaraldehyde fixation of Ia-positive A20.2JAD (A20) and P388D1 stimulator cells had different effects on T-cell activation. A20 cells fixed with glutar...

Journal: :Journal of cell science 1983
C Capo Z Mishal V Balloy A M Benoliel P Bongrand

The murine macrophage-like cell line P388D1 ingests immunoglobulin-coated sheep red cells (IgG-SRC) poorly, but after 3 days incubation in the presence of 1.5% dimethyl sulphoxide (DMSO), it becomes highly phagocytic. We used this model to correlate triggering of phagocytosis with some surface properties of P388D1 cells, possibly involved in recognition or engulfment of particles. The accessibi...

Journal: :Infection and immunity 1989
B Wu-Hsieh D H Howard

Histoplasma capsulatum, a facultative intracellular parasite of macrophages, grows within mononuclear cells of the P388D1 and IC-21 cell lines with a generation time comparable to that with which it grows in normal resident peritoneal macrophages (10 +/- 2 h). Recombinant murine gamma interferon (rMuIFN-gamma) activates P388D1 cells to express la antigens but not to inhibit the intracellular gr...

Journal: :Journal of cell science 1995
D Proudfoot D P Parrott D E Bowyer

P388D1 macrophage-like cells have previously been shown to produce both mitogenic and inhibitory regulators of porcine smooth muscle cell (pSMC) growth. The mitogenic activity was shown to have a molecular mass of > 10 kDa while the inhibitory activity was in the range of 2-6 kDa. In the present study, we present a novel dialysis culture system where P388D1 cells were grown in dialysis membrane...

Journal: :Infection and immunity 1994
T E Lane G C Otero B A Wu-Hsieh D H Howard

The antihistoplasma activity of recombinant murine gamma interferon (rMuIFN-gamma)-treated macrophages of the RAW 264.7 cell line depends on the generation of nitric oxide (NO.) from L-arginine. Macrophages of the P388D1 cell line treated with rMuIFN-gamma do not produce NO. or inhibit the intracellular growth of Histoplasma capsulatum. NO. is generated by the inducible enzyme nitric oxide synt...

Journal: :The Journal of clinical investigation 1988
S H Gianturco A H Lin S L Hwang J Young S A Brown D P Via W A Bradley

Murine P388D1 macrophages have a receptor pathway that binds human hypertriglyceridemic very low density lipoproteins (HTG-VLDL) that is fundamentally distinct from the LDL receptor pathway. Trypsin-treated HTG-VLDL (tryp-VLDL), devoid of apolipoprotein (apo)-E, fail to bind to the LDL receptor, yet tryp-VLDL and HTG-VLDL cross-compete for binding to P388D1 macrophage receptors, indicating that...

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