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In dieser in vivo Studie beschreiben wir den Typ, die Kinetik und die mikrovaskulare Lokalisation der Rekrutierung von CD4+ T-Zellen in der postischamischen Leber. CD4+ T-Zellen interagieren mit Thrombozyten in den postischamischen Sinusoiden; diese Interaktion wird durch Bindung des thrombozytaren CD62P an den entsprechenden Liganden PSGL-1 auf T-Zellen mediiert, wahrend die reziproke Aktivierung beider Zelltypen durch die CD40-CD40L-Interaktion vermittelt wird. CD4+ T-Zellen aktivieren das sinusoidale Endothel, und verstarken die I/R-induzierte Thrombozytenakkumulation sowie den mikrovaskularen hepatischen I/R-Schaden durch die CD40-CD40L and CD28-B7 Signalwege ohne Beteiligung von MHC Klasse II-Molekulen.

Nitric oxide production by the inducible NO-synthase in the synovium and chondrocytes is known to be enhanced during chronic joint inflammation and aseptic loosening of joint prostheses. Due to the distinct side effects of non-selective NO-inhibitors on the macro- and microhemodynamics, we investigated the in vivo changes after selective (N-iminoethyl-L-lysine (NIL)) versus non-selective NO-synthase inhibition (NG-nitro-L-arginine methyl ester (L-NAME)) in the synovium of the mouse knee joint. Our results show a significant decrease in the functional capillary density and an increase in the leukocyte accumulation after L-NAME injection. In contrast, NIL did not alter the microhemodynamics or the leukocyte-endothelial cell interaction in the synovium, indicating its potential use for therapeutic selective inhibition of iNOS in joint inflammation.

The microcirculation is the organ that provides the direct link between blood and tissue, and thereby between the whole organism and the single cell. Modern microcirculation research in experimental surgery is characterized by the use of high-resolution video fluorescence microscopy and quantitative computer-assisted image analysis coupled with the techniques of molecular biology and transgenic or knockout gene technology. These advances should improve knowledge about surgically relevant physiologic and pathophysiologic phenomena at the interface between blood and tissues and help us to understand the initial molecular mechanisms leading to organ dysfunction following inflammation, ischemia-reperfusion, and transplantation.

Fibrosing alveolitis (FA) is a common and often fatal complication of systemic sclerosis (SSC). The purpose of this study was to characterize the fibrotic process within the lungs using bronchoalveolar lavage fluid (BALF). We investigated 25 healthy controls (CON) and 85 SSC patients. In 61 patients (72%) lung function tests, clinical, and radiological findings indicated manifest FA, whereas 24 patients (28%) where free of significant lung disease. Of the latter, 12 had pathologic BAL differential cell counts (= subclinical alveolitis; SUB), 12 had normal BAL cytology (NOR). BAL samples were analysed for chemoattractant activity (CAA) for fibroblasts using Boyden chambers. Procollagen-III-Peptide (P-III-P) and Laminin fragment P1 (Lam-P1) were measured radioimmunologically. CAA (expressed as % of the effect of conditioned medium) was increased in FA and SUB (CON: 17.3 +/- 3.2; FA: 40.8 +/- 5.8, p0.01 vs. CON; SUB: 58.6 +/- 11.8, p0.01 vs. CON; NOR: 23.7 +/- 6.3; n.s.). Lam-P1 [U/ml ELF] was also elevated in FA and SUB patients (CON: 0.90 +/- 0.17; FA: 2.07 +/- 0.48, p0.05 vs. CON; SUB: 2.61 +/- 1.14, p0.05 vs. CON; NOR: 1.05 +/- 0.35, n.s. vs. CON). P-III-P [U/ml ELF] was elevated in FA patients (CON: 8.3 +/- 1.1; FA: 26.9 +/- 5.5, p0.001 vs. CON) but not in SUB or NOR (SUB: 10.2 +/- 0.7, NOR: 7.9 +/- 2.9; n.s.). There was no significant relationship between P-III-P and LAM-P1 values in ELF and serum, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)

High resolution, narrow section CT examinations of the lungs were carried out on 21 Javanese macaques (five controls) shortly before the conclusion of 27 months exposure to quartz and/or high pressure. The aim was to establish morphometric CT data for differentiating and quantifying normal and abnormal findings. The results show that the technique has a high sensitivity for demonstrating the pathological lung changes. Final validation depends upon the use of respiratory physiology and biochemical, cytological, and histomorphometric data.