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Biomedical subjects

M A Lande

Publications and source records attributed to M A Lande.

At least 19 recordsLinked to original sources

In vivo characterization of host and bacterial protease expression during Pseudomonas aeruginosa corneal infections in naive and immunized mice.

PURPOSE: The corneal destruction resulting from P. aeruginosa keratitis is thought to be due, in part, to the actions of host and bacterial proteases on corneal tissue. The intent of the current study was to compare host and bacterial protease expression in the ocular tissues of mice that have been shown to be susceptible to corneal infection with mice that have been protected from such infection as a result of prior immunization. METHODS: Supernatants of infected corneal homogenates from naive mice or from mice immunized as a result of prior corneal infection or that had been immunized against bacterial protease were analyzed by gelatin zymography for the presence of host gelatinases and bacterial proteases at various times after infection. In addition, studies were carried out to examine the effect of immunization with bacterial protease on numbers of ocular bacteria. RESULTS: Mice that were protected against the tissue destruction during infection were found to have reduced proteolytic activity in corneal tissues when compared with susceptible mice. More specifically, the resistant mice displayed lower levels of bacterial alkaline protease, latent MMP-2, and both the active and latent forms of MMP-9. In addition, immunization against either bacterial alkaline protease or elastase failed to reduce bacterial numbers in ocular tissues from 6 to 72 hours after infection. CONCLUSIONS: These results suggest that increased proteolytic activity in ocular tissues during P. aeruginosa infection may contribute to the irreversible corneal damage observed during the infection.

Animals↗

Proteoglycans from osteoarthritic human articular cartilage influence type II collagen in vitro fibrillogenesis.

Collagen fibrils were formed in the presence of dermatan sulfate (DSPG) and high density (HDPG) proteoglycans isolated from human adult knee femoral articular cartilage. Eroded cartilage had a higher percentage of DSPGs in the extracted proteoglycans than normal cartilage (p = .018). The dermatan sulfate proteoglycans (DS-PGI and DS-PGII) were detected in normal and osteoarthritic cartilage. DSPGs compared to HDPG inhibited in vitro collagen fibrillogenesis producing a longer lag phase (p less than .05) and a slower rate of fibril formation (p less than .05). DSPGs from eroded osteoarthritic cartilage alone or in combination with HDPG produced a longer lag phase than DSPGs from normal cartilage alone or in combination with HDPG (p less than .05). The inhibition of fibrillogenesis by DSPGs suggests that collagen fibril formation in vivo may be abnormal due to the influence of molecular changes in proteoglycan as well as an increased proportion of DSPGs occurring in osteoarthritic cartilage. Abnormal fibril formation may produce a weakened cartilage matrix, thus contributing to an accelerated process of cartilage degeneration in osteoarthritis.

Cartilage, Articular↗

A human cartilage metalloproteinase with elastolytic activity.

A metalloproteinase with elastolytic properties found in human fetal and osteoarthritic cartilage could not be detected in normal adult cartilage. During extraction the enzyme appeared to be mostly associated with cartilage proteoglycans, from which it can be separated by ion exchange chromatography. This enzyme migrated during electrophoresis with an apparent molecular weight of 62,000 daltons and was found to be fully activated in the tissue under the study conditions. The enzyme showed a preference for substrates rich in non-polar amino acid residues and was capable of breaking down elastin and casein at neutral pH. The enzyme activity can be inhibited by chelating agents and specific affinity reagents, chloroketones, and is not inhibited by other proteinase inhibitors such as PMSF, aprotinin and alpha-1-antitrypsin. This enzyme may play a significant role in conditions demanding rapid cartilage matrix turnover and/or remodeling, such as normal embryonic development or osteoarthritis.

Adult↗

Induction of collagen synthesis in cultured human fibroblasts by live Schistosoma mansoni eggs and soluble egg antigens (SEA).

There is a dearth of knowledge on the tissue fibrosis that contributes to the pathology of schistosomiasis mansoni. The present study was designed to test the direct effect of live schistosome eggs and soluble egg antigens (SEA) on cultured normal human fibroblasts. Coincubation for 3 days of fibroblast monolayers with 100-500 live eggs/ml medium or equivalent amounts of SEA caused enhanced incorporation of labelled proline. The newly synthesized polypeptides were sensitive to purified collagenase enzyme activity. Collagen synthesis was also verified by measuring increased hydroxyproline content in fibroblasts. Whereas low numbers of eggs stimulated fibroblast activity, 500 eggs/ml medium caused a disarray in the arrangement of cells, with cytoplasmic granulation, cell detachment and death. These results indicate that fibroblast stimulation and collagen synthesis may also be triggered by the direct action of egg secretions on tissue fibroblasts.

Animals↗

Corneal and scleral collagen fiber formation in vitro.

We have investigated the role of structural differences in collagen molecules and the effect of proteoglycan preparations on the control of collagen fibril formation. Collagen and proteoglycans were extracted, purified and characterized from two structurally and functionally different connective tissues, rabbit corneal stroma and sclera. Corneal collagen was found to form fibers 6- to 7-times more slowly than scleral type I collagen. Proteoglycans from both sources retard fibrillogenesis, with corneal proteoglycans having approximately 3-times the effect observed with scleral proteoglycans. The morphology of the fibers formed was normal in all cases. Therefore, the changes observed may reflect a true control mechanism related to the strict morphological arrangement associated with corneal transparency.

Amino Acids↗

Phagocytic properties of human keratocyte cultures.

The uptake of polystyrene latex beads (approximately 0.75 micrometers) and glutaraldehyde-treated erythrocytes by human corneal stromal keratocytes maintained in culture has been studied. Combined phase-contrast and scanning electron microscopic observations on individual cells after exposure to either beads or erythrocytes demonstrated that the majority of these particles were present intracellularly. Transmission electron microscopy revealed that the beads were membrane-bound within the cytoplasm of these cells. Thus the human keratocytes in culture are phagocytic and able to internalize particles ranging in size from approximately 0.75 to 6 micrometer. Kinetic studies showed continuous uptake of the polystyrene latex beads for at least 72 hr, with an approximate linear uptake rate between 4 and 48 hr. The extent of bead uptake was dependent on the initial bead concentration. The human keratocyte cultures were markedly more phagocytic than human skin fibroblasts or rabbit chondrocytes. It was also found that after extensive bead uptake the normal growth pattern of the keratocytes was affected. It is suggested that the phagocytic ability of the human keratocytes is involved in the turnover of the corneal stromal matrix as well as in the initial response of this avascular tissue to injury or bacterial infection.

Cells, Cultured↗

Direct association of messenger RNA with microsomal membranes in human diploid fibroblasts.

Messenger RNA (mRNA) of membrane-bound polysomes in a membrane fraction of WI-38 cells remains associated with the microsomal membranes even after ribosomes and their nascent polypeptide chains are removed by using puromycin in a high salt buffer or by disassembling the ribosomes in a medium of high ionic strength lacking magnesium. mRNA either was specifically labeled in the presence of actinomycin D, or it was recognized by virtue of its affinity for oligo-dT. Poly A segments in bound mRNAs have an electrophoretic mobility in acrylamide gels which is characteristic of cytoplasmic mRNAs and corresponds to 150-200 adenyl residues. Extensive RNase treatment did not lead to release of the poly A segments of membrane-associated mRNA molecules either from an intact membrane fraction or from a membrane fraction previously stripped of ribosomes. On the other hand, RNase treatment led to the release and digestion of the nonpoly A segments of the mRNA molecules, indicating that the site of attachment of mRNA to the ER membranes is located near or at the 3' end of the molecule which contains the poly A. A direct association of mRNAs and endoplasmic reticulum membranes is considered in a modelto explain the assembly of bound polysomes and protein synthesis in a membrane-associated apparatus.

Adenosine Monophosphate↗