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Confocal Laser Scanning Microscopy of Leukocyte Adhesion in the Microcirculation of the Inflamed Rat Knee Joint Capsule
Author(s) -
FINKENAUER VOLKER,
BISSINGER THOMAS,
FUNK RICHARD H.W.,
KARBOWSKI ALFRED,
SEIFFGE DIRK
Publication year - 1999
Publication title -
microcirculation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.793
H-Index - 83
eISSN - 1549-8719
pISSN - 1073-9688
DOI - 10.1111/j.1549-8719.1999.tb00096.x
Subject(s) - intravital microscopy , microcirculation , capsule , pathology , joint capsule , carrageenan , chemistry , inflammation , medicine , anatomy , biology , botany , biochemistry
ABSTRACT Objective : The aim of the study was to develop a model of intravital microscopy of the microcirculation of the rat knee joint capsule in acute inflammation with the help of confocal laser scanning microscopy (CLSM). Methods : The microvascular architecture of the joint capsule was investigated by the use of corrosion casting techniques. Knee joint capsule microcirculation of anesthetized rats could be visualized by dissection of the ligamentum infrapatellare rectum and application of a CLSM. Rhodamine 6G was used as a leukocyte marker. An acute arthritis was induced by intraarticular injection of 0.1 mL of 1% Carrageenan solution. Each experiment lasted for 3 h. Leukocyte adhesion (LA) was measured in 100 µm of vessel length. Leukocyte‐rolling velocity (Vwbc), systemic leukocyte count (WBC), and differential blood count (DBC) were monitored in defined intervals. Finally, myeloperoxidase (MPO) activity in frozen‐tissue homogenate served as a parameter of neutrophil content. Results : Leukocyte adhesion in carrageenan‐treated animals was 9.9 +/−0.2 leukocytes / 100 µm vessel (mean +/−SD; n = 6), while sham ‐ treated animals had 2.8 +/−0.2. Monoclonal antibodies (MAb) to α4 integrin (0.2 mg/kg) reduced LA to 2.6 +/−0.1 ( p < 0.01). Vwbc/γ quotients were 0.37 µms/s in control animals and 0.53 µms/s in anti‐α4‐treated animals ( p < 0.01). Changes in DBC were marked by lymphopenia and granulocytosis after 180 min. At this time point‐control animals had 5.1 G/L LC and 2.6 G/l PMN. Animals treated with unspecific antibody had 4.7 G/L LC and 4.9 G/L PMN, while anti‐α4‐treated animals had 10.6 G/L LC and 2.4 G/L PMN. Photometrically determined extinction of oxidized tetramethylbenzidine (TMB; measure for MPO content) was 1.058 +/− 0.555 in control animals and 0.245 +/− 0.093 in sham‐treated animals. Tissue homogenate from unspecific IgG treated group had 0.776 +/− 0.140 and from anti‐α4‐group 0.334 +/− 0.155 ( p < 0.05). Conclusions : Confocal laser scanning microscopy is a tool for the study of the microcirculation in nontransparent organs. The microcirculation of the acutely inflamed rat knee joint capsule can serve as a model of integrin‐mediated LA in vivo . Antiadhesive treatment of animals can reduce the tissue infiltration with inflammatory cells.