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. 1999 Jun 7;189(11):1783-9.
doi: 10.1084/jem.189.11.1783.

Thioredoxin, a redox enzyme released in infection and inflammation, is a unique chemoattractant for neutrophils, monocytes, and T cells

R Bertini  1 , O M Howard, H F Dong, J J Oppenheim, C Bizzarri, R Sergi, G Caselli, S Pagliei, B Romines, J A Wilshire, M Mengozzi, H Nakamura, J Yodoi, K Pekkari, R Gurunath, A Holmgren, L A Herzenberg, L A Herzenberg, P Ghezzi
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Thioredoxin, a redox enzyme released in infection and inflammation, is a unique chemoattractant for neutrophils, monocytes, and T cells (VSports注册入口)

R Bertini et al. J Exp Med. .

Abstract

Thioredoxin (Trx) is a ubiquitous intracellular protein disulfide oxidoreductase with a CXXC active site that can be released by various cell types upon activation. We show here that Trx is chemotactic for monocytes, polymorphonuclear leukocytes, and T lymphocytes, both in vitro in the standard micro Boyden chamber migration assay and in vivo in the mouse air pouch model. The potency of the chemotactic action of Trx for all leukocyte populations is in the nanomolar range, comparable with that of known chemokines VSports手机版. However, Trx does not increase intracellular Ca2+ and its activity is not inhibited by pertussis toxin. Thus, the chemotactic action of Trx differs from that of known chemokines in that it is G protein independent. Mutation of the active site cysteines resulted in loss of chemotactic activity, suggesting that the latter is mediated by the enzyme activity of Trx. Trx also accounted for part of the chemotactic activity released by human T lymphotropic virus (HTLV)-1-infected cells, which was inhibited by incubation with anti-Trx antibody. Since Trx production is induced by oxidants, it represents a link between oxidative stress and inflammation that is of particular interest because circulating Trx levels are elevated in inflammatory diseases and HIV infection. .

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Figures

Figure 6
Figure 6
Trx-induced leukocyte recruitment in the air pouch in mice. 1 μg of Trx was injected in the air pouch as described in Materials and Methods. Control mice were injected with vehicle only. 4 h later, the cells in the air pouch were recovered, counted, and analyzed by FACS®. ○, mean of seven control mice; •, Trx-treated mice (n = 7).
Figure 1
Figure 1
Chemotactic effect of Trx on human PMNs, monocytes, and T cells. The average number of cells migrated in five oil immersion fields ± SD using different concentrations of human recombinant Trx (•) or boiled (30 min at 100°C) human recombinant Trx (○) are shown. The response to a known chemokine (left panel, IL-8; center panel, MCP-1; right panel, RANTES) is also shown (⋄) as a reference.
Figure 2
Figure 2
Chemotactic activity of Trx is inhibited by an anti-Trx antibody. Trx was incubated for 15 min at 37°C with 0.5 μg/ml goat anti– human Trx or a control antibody (anti-GST). Trx was then assayed for chemotactic activity for monocytes at the concentration of 2.5 nM, as described above. Data are mean ± SD of triplicate samples.
Figure 3
Figure 3
Chemotactic activity of Spirulina TRX, Trx(SGPS) mutant, or glutaredoxin on human PMNs and monocytes. The proteins were tested at the indicated concentrations, as described in the legend to Fig. 1. The data show the number of cells migrated in five oil immersion fields using different concentrations of the test protein. Data are mean ± SD of triplicate samples.
Figure 4
Figure 4
Trx does not increase cytosolic Ca2+ in human monocytes or PMNs. Traces represent levels of [Ca2+]i in single adherent monocytes (A and B) or PMNs (C and D) in response to 30 ng/ml (2.5 nM) Trx (A and C), 25 ng/ml (3 nM) IL-8 (D), or 50 ng/ml (6 nM) MCP-1 (B). Traces are representative of 12–32 cell recordings (7 donors, 3–5 cells per coverslip). Arrows indicate the addition of agents to the bathing medium, which causes a spike in the trace due to exposure to light.
Figure 5
Figure 5
Chemotactic activity of Trx on monocytes is not inhibited by PT. Monocytes were incubated with 1 μg/ml PT for 90 min at 37°C, then washed to remove PT and used for chemotaxis experiments with Trx (30 ng/ml) or MCP-1 (25 ng/ml), as described above. Data from two independent experiments are shown. Data are mean ± SD of triplicate samples. *P < 0.05 versus control by Student's t test.
Figure 7
Figure 7
Trx is a component of the chemotactic activity for PMNs released by the HTLV-1–transformed cell line MT4. Supernatants from MT4 cells or control media were treated for 15 min at 37°C with goat anti–human Trx (0.5 μg/ml) or a control antibody (anti-GST). Supernatants were then assayed for chemotactic activity on PMNs as described above. **P < 0.05 versus control by Student's t test.
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