Proportion Of Ia Research Articles

The Distributions of Voltage-Gated K+ current Subtypes in Different Cell Sizes from Adult Mouse Dorsal Root Ganglia.

Voltage-gated K+ (KV) currents play a crucial role in regulating pain by controlling neuronal excitability, and are divided into transient A-type currents (IA) and delayed rectifier currents (IK). The dorsal root ganglion (DRG) neurons are heterogeneous and the subtypes of KV currents display different levels in distinct cell sizes. To observe correlations of the subtypes of KV currents with DRG cell sizes, KV currents were recorded by whole-cell patch clamp in freshly isolated mouse DRG neurons. Results showed that IA occupied a high proportion in KV currents in medium- and large-diameter DRG neurons, whereas IK possessed a larger proportion of KV currents in small-diameter DRG neurons. A lower correlation was found between the proportion of IA or IK in KV currents and cell sizes. These data suggest that IA channels are mainly expressed in medium and large cells and IK channels are predominantly expressed in small cells.

Lung‐phase immunity to Schistosoma mansoni: definition of alveolar macrophage phenotypes after vaccination and challenge of mice

Phenotypic changes in murine alveolar macrophages have been described in response to vaccination with irradiated cercariae and to a subsequent challenge with normal parasites. Flow cytometric analysis was used to quantify the proportions of cells strongly positive for a number of macrophage surface markers, detected by a panel of monoclonal primary antibodies and fluorescent secondary antibodies. The proportion of Ia+ macrophages sampled by bronchoalveolar lavage increased 5-fold over days 14 to 28 post-vaccination. This upregulation of Ia was accompanied by a sharp decrease in F4/80 expression between days 14 and 21. The low percentage of F4/80+ cells persisted for several weeks after vaccination, and no further change was stimulated by challenge parasites. These altered characteristics are consistent with the 'activation phenotype' induced by other infectious agents. After challenge of immune mice, further changes in macrophage phenotype were slight compared to the responses elicited by vaccination, or to those induced in the challenge control group; Ia expression increased to about three times normal levels. The phenotypic changes correspond both in magnitude and timing with the pattern of alveolar macrophage activation determined in a previous study. The limited changes in phenotype of alveolar macrophages from immunized mice after challenge could indicate that these cells become refractory to reactivation. Overall, the altered macrophage phenotype after vaccination and challenge provides circumstantial evidence for the action of cytokines, particularly interferon-gamma, in lung-phase immunity to schistosomes.

Omental dendritic cells: la expression and relation to macrophages

Rat omental dendritic cells (ODC) occur in two forms, mainly spindle-shaped, Ia-, on the surface, and stellar, Ia+ within the omentum. Like macrophages, most ODC label with W3/25 mAb and have a demonstrable activity of non-specific esterase, acid phosphatase and ATPase. Up to 30% of ODC are actively phagocytic. The proportion of Ia+ ODC rises 7 days after ip antigenic stimulation and there seems to be a reciprocal development of Ia positivity and phagocytic capacity between ODC and macrophages 3 and 5 days after ip immunization. ODC contribute to the overall fluctuation of Ia expression in the entire omentum after immunization. Ia+ ODC display a linear arrangement along preilymphatic spaces and may be related to the formation of new lymph vessels. They also constitute the stroma of pseudofollicles containing clusters of what are presumably T-helper lymphocytes closely attached to ODC, scattered suppressor T lymphocytes and B cells accumulating in later stages at the immune response.

Ia-Positive T Cells in Normal Human Peripheral Blood by Indirect Antiglobulin Rosetting Reaction (IARR)

In this study we intended to Characterized the Ia-antigen positive (Ia+) T cells in peripheral blood from normal individuals, detecting by indirect antiglobulin rosetting assay utilizing monoclonal anti-human DR antibody, which reacted with the human DR antigen framework.Higher percentage of Ia+ T cells than those described previously by using indirect immunofluorescence was observed in normal peripheral blood. After PHA, Con A or PWM activation, the proportion of Ia+ T cells increased up to about 30% of T cells. It also rose rapidly after inoculation with PPD in sensitized individuals only. The proportion of Ia+ T cells well correlated with the proportion of Tr cells. It was also revealed that Ia+ T cells were enriched in the OKT+4 cell-rich population than OKT+8 population from T cells of normal unstimulated individuals.

Functional heterogeneity of culture-grown bone marrow-derived macrophages. II. Lymphokine stimulation of antigen-presenting function.

Abstract The activation of immunostimulatory activity and Ia expression was studied in pure populations of murine macrophages (M phi) grown in vitro from bone marrow precursor cells in the presence of L cell-conditioned medium as the source of colony-stimulating factor. During exponential growth, the M phi developed maximal Ia-dependent antigen-presenting activity as detected by the induction of antigen-specific T cell proliferation, but the proportion of Ia+ M phi was low (less than 10%). Fractionation of the M phi according to size by velocity sedimentation resulted in concentration of the antigen-presenting cells in the smallest fraction, but the enrichment of Ia+ M phi in this fraction was less than twofold. All fractions also showed comparable degrees of antigen uptake regardless of their T cell-stimulating activity. Thus Ia and antigen, although obviously essential, are insufficient for full manifestation of antigen-presenting function. Activation of M phi with lymphokines from Mycobacterium-activated lymph node cells resulted in enhanced Ia expression in all fractions, but only small M phi showed an enhancement in antigen presentation. Large activation M phi were found to exert an immunosuppressive effect that probably neutralized any augmentation of stimulatory activity. thus heterogeneity can be demonstrated in i) the function of unstimulated M phi, ii) the responsiveness of subsets to stimulation, and iii) the manifestation of activated functions.

Ia antigen on the surface of a subfraction of T cells that bear Fc receptors for IgG.

Human peripheral blood T cells and T cell subpopulations were studied for the presence of Ia-like antigen, by using indirect immunofluorescence with heterologous rabbit anti-Ia antisera. In 13 normal subjects the percentage of T cells staining with the anti-Ia reagent was 2 to 5% and appeared limited to the T gamma subfraction. After concanavalin A (Con A) or phytohemagglutinin (PHA) activation, the proportion of Ia(+) T cells increased due to an increase in the percentage of T gamma cells bearing Ia-like antigen as well as an increase in the proportion of T gamma cells in the T cell fraction.

Ia determinants on stimulated human T lymphocytes. Occurrence on mitogen- and antigen-activated T cells.

Human T-cell blasts were generated by stimulation with mitogens and antigens. A proportion of these blasts expressed Ia antigens detectable by immunofluorescence with both allo- and hetero-antiserums. The maximal expression of Ia antigens was delayed and usually occurred after the peak of blastogenesis. Among the three mitogens used, pokeweed mitogen (PWM) was most effective in giving a high percentage and intense Ia staining of T-cell blasts. Phytohemagglutinin and concanavalin A blasts gave weaker and lower percentages of Ia staining. Activation by alloantigens and soluble antigens such as tetanus toxoid and purified protein derivative resulted in Ia expression on T cells comparable to PWM stimulation. Depletion of Ia+ cells from freshly isolated T cells with anti-Ia and complement decreased subsequent Ia expression, suggesting that a proportion of Ia+ blasts were derived from Ia-bearing peripheral blood T cells. When the specificities of the Ia antigens on T-cell blasts were examined with alloantiserums, it was evident that the T blasts expressed similar HLA-DR determinants to those on B cells from the same donor; occasional minor differences between stimulated T cells and autologous B-cell lines or fresh B cells were encountered.

Characterization of the target cell antigen in I region-mediated lympholysis

Cytotoxic T lymphocytes (CL) can be produced by culturing I region disparate spleen cells as previously reported. More recently, it was shown that these CL can lyse other target cells which shared only the I-A subregion with the stimulator cells, i.e., lysis of these target cells is not H-2K/D restricted. Since I region-mediated lympholysis represents the only strong exception ruling out the obligatory role for H-2K/D products in mediating cytolysis of target cells, it is important to characterize further the target antigen recognized by CL in this system. A.TH anti-A.TL or (A.TL × B10.A) Fl anti-B10.HTT CL were generated in a 4-day primary culture system. The CL, shown to be Thy-1 +, are able to kill targets that share only the central region of H-2 with the stimulator cells. These I region-specific CL can also lyse target cells that express a cross-reacting Ia antigen with the stimulator cells. Incompatibilities at IA/IB and IE/IC gave stronger cell-mediated lympholysis than incompatibilities at IA/IB only. Experiments involving the use of cold target competition, inhibition by specific anti-Ia serum, and target cells containing different proportions of Ia + cells, strongly suggest that the target antigens recognized by the CL are in fact Ia antigens.