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D M Makker

Publications and source records attributed to D M Makker.

2 recordsLinked to original sources

Transferrin synthesis by inducer T lymphocytes.

Transferrin (Tf) is a growth factor that transports iron in plasma. It is essential for proliferation of activated T lymphocytes. Previous studies have suggested that peripheral blood cells are capable of synthesizing Tf. Using in situ hybridization techniques and human Tf complementary DNAs as probes, peripheral blood cells have been examined for sites of Tf messenger RNA (mRNA) transcription. The studies described here demonstrate that Tf is synthesized by a specific subset of T lymphocytes, the T4+ inducer subset. T lymphocyte proliferation is dependent upon the presence of both interleukin 2 (IL-2) and Tf, even though resting cells do not possess receptors for either. The present studies indicate that during T cell activation, induction of IL-2 mRNA transcription and IL-2 receptor expression precede the transcription of Tf mRNA and expression of Tf receptors, respectively. These events in turn precede the initiation of DNA synthesis. Transferrin and its receptor appear to be involved in an autocrine pathway which is functionally linked to the IL-2/IL-2 receptor autocrine loop.

Cell Cycle↗

A simple technique for detecting the antigen of Heymann nephritis in glomeruli by immunofluorescence.

In the past, on routine 2-4 micron renal cortical frozen sections it has been difficult to demonstrate the putative glomerular antigen of Heymann nephritis (HN) by indirect immunofluorescence. We describe, herein, a technique which overcomes this difficulty and can be used to reliably detect glomerular antigen(s). The technique consists of first isolating individual glomeruli by sieving and then preparing a suitable frozen block that contains only glomeruli and no tubules to cut 2-4 micron frozen sections. Using this technique and the putative heterologous and autologous antibodies of HN we have succeeded in showing a clear and convincing reactivity of these antibodies with the glomerular antigen(s) by indirect immunofluorescence. In addition the results obtained provide at least a partial explanation for the puzzling discrepancy observed by many investigators of the findings of either no or poor reactivity of these antibodies to normal glomeruli on rat kidney sections in vitro and their readily demonstrable glomerular localization in vivo upon intravenous injection to normal rats. This technique may also prove useful in detecting reactivity of antibodies to other glomerular antigens that are difficult to demonstrate on routine frozen sections of kidney.

Animals↗