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Biomedical subjects

C B Rich

Publications and source records attributed to C B Rich.

At least 37 records · Page 2Linked to original sources
PubMed1989

Evidence for insulin-like growth factor-I regulation of chick aortic elastogenesis.

The potential role of insulin-like growth factor-I (IGF-I) as a modulator of chick aortic embryogenesis was examined. Studies were designed to investigate the in vivo relationships between embryonic IGF-I serum concentrations, liver and aortic IGF-I mRNA steady-state levels and the inception and perpetuation of aortic elastogenesis. In addition to aortic tissue, elastogenesis was measured in heart and lung tissues in order to compare the responses of functionally unique elastin-containing tissues to the developmental appearance of IGF-I in embryonic serum. Our results demonstrate that the induction of aortic tropoelastin mRNA steady-state levels coincides with a major increase in serum IGF-I concentration. This is not the case with either lung or heart elastogenic responses. All three tissues examined (aorta, lung, and heart) exhibited different developmental patterns of tropoelastin mRNA steady-state levels during the embryonic ages studied (8- through 10-day). Only aortic tropoelastin mRNA levels paralleled the rise and fall of IGF-I serum levels. Steady-state levels of liver IGF-I mRNA peaked one day (9-day) prior to detectable IGF-I serum levels but otherwise mirrored the gradual, but steady decrease in IGF-I serum levels through 16-day. Aortic tissue also expresses IGF-I mRNA beginning at 8-day and continuing throughout the embryonic ages examined (16-day). Although the relative levels of aortic IGF-I mRNA are very low in comparison to corresponding mRNA levels in liver, the fact that IGF-I mRNA is transcribed in the aorta points to the possibility that autocrine and/or paracrine mechanisms of IGF-I action may be operative in aortic elastogenesis.

Animals↗
PubMed1988

Synthesis of soluble and insoluble elastins in cultures of chick aortic cells.

Aortic cells were isolated from 9- and 12-day embryonic chick aortas and cultured for varying periods after first passage. Cells obtained from 9-day tissue remained indefinitely as monolayers and possessed a relatively low rate of tropoelastin synthesis. Cells obtained from 12-day tissue remained monolayers for 4 to 8 days, after which time portions of the culture contracted into matrix containing chemically definable insoluble elastin and forming desmosine cross-links. The rate of tropoelastin synthesis was significantly higher in the 12-day derived cells suggesting that these cells had been committed to elastogenesis in vivo and retained this commitment in vitro. A chick tropoelastin cDNA was obtained and partially characterized from a lambda gt11 expression cDNA library. Using the tropoelastin cDNA probe, measurement of the steady-state level of tropoelastin revealed that the increased rate of tropoelastin synthesis in the 12-day cells was accompanied by a significant increase in the level of tropoelastin mRNA steady-state levels. The aortic cell cultures present an important model system for extending studies of chick aortic elastogenesis. The aortic cell cultures synthesize tropoelastin at a rate 10% less than the corresponding organ culture. Significantly, the production of tropoelastin is productive in formation of insoluble, chemically definable elastin. The definition of insoluble includes both amino acid composition and desmosine formation.

Amino Acids↗
PubMed1987

Evidence for the existence of three chick lung tropoelastins.

Three tropoelastin polypeptides are identified among the cell-free translation products of chick embryo lung mRNAs and organ cultures extracts. The tropoelastins are distinguished by one and two dimensional gel electrophoretic systems and are all immunoreactive with monospecific chick tropoelastin antiserum. The ratio of the three tropoelastins does not vary significantly between 10 and 16 days of lung embryogenesis. The third tropoelastin (c) is found to co-migrate with tropoelastin b on SDS-polyacrylamide gel electrophoresis but is visible after cyanogen bromide cleavage of reticulocyte lysate proteins. Immunoprecipitates from lung organ culture also contain tropoelastins a, b and c.

Animals↗
PubMed1987

Insulin-like growth factor I, somatomedin C, induces the synthesis of tropoelastin in aortic tissue.

The action of IGF-I (insulin-like growth factor I) on the synthesis of tropoelastin in chick embryonic aortae was examined. Maximal and selective stimulation of the relative (40%) and absolute (145%) rates of tropoelastin synthesis over control occurred at an IGF-I concentration of 100 ng/ml of medium. Parallel to the increase in synthesis was a 92% increase in the amount of tropoelastin activity per 100 ng of poly (A)+ RNA translated in a cell-free system. The relative rate of tropoelastin synthesis achieved at maximal stimulation is greater than that observed during normal aortic embryogenesis. The stimulatory action of the hormone on elastin synthesis appears to be at a pretransitional level perhaps involving increased transcription or stabilization of the tropoelastin mRNAs. These results suggest that IGF-I may play a key role in the regulation of elastogenesis in arterial tissue.

Animals↗
PubMed1987

Pulmonary fibroblasts: a model system for studying elastin synthesis.

Pulmonary interstitial fibroblasts were isolated from 4-day neonatal rat lung and cultured for varying periods of time after first passage. The ability of the cells to synthesize both soluble and insoluble elastin was examined by biochemical, immunological, and ultrastructural techniques. The cells synthesize a tropoelastin of 75,000 daltons which is cross-linked in the extracellular matrix to form sufficient amounts of insoluble elastin to be characterized directly by amino acid analysis. Although the cells produce a soluble form of elastin immediately after confluency and the deposition in the matrix begins shortly thereafter, the actual chemical definition of alkali-resistant elastin does not occur until 4 weeks after confluency. The apparent molecular weight of tropoelastin synthesized by the cells agrees with the molecular size of tropoelastin found in organ culture of neonatal lungs. The pulmonary fibroblast cultures provide an important model system for examining the regulation and response of elastin synthesis in lung interstitium.

Animals↗
PubMed1986

Tropoelastin synthesis in fetal bovine tissues.

Tropoelastin was examined in bovine lung, aortic and ligament tissues using both organ culture and cell-free translation systems. The bovine tissues synthesized two tropoelastin polypeptides of approximately 70,000 and 68,000 daltons. Two polypeptides were also seen amongst the translation products directed by mRNAs isolated from each of the individual tissues. Both proteins were shown to be tropoelastins directly by immunoprecipitation with specific antibody and limited NH2-terminal sequence analyses and indirectly by two-dimensional gel electrophoresis. The finding of two forms of tropoelastin is similar to that previously reported in chick tissues although the apparent molecular weights of the tropoelastins differ between the two species. Another interesting observation is that the proportion of the two tropoelastins differs amongst the three fetal tissues examined. This situation is similar to the differences seen in the ratio of tropoelastin a and be between embryonic chick lung and aortic tissues.

Animals↗
PubMed1984

Isolation of tropoelastin a from lathyritic chick aortae.

Tropoelastin a was isolated from lathyritic chick aortae by using severe denaturing conditions for the initial extraction. The amino acid composition of this new species of tropoelastin is elastin-like in its high proportion of proline, glycine, alanine and valine. However, it differs from authentic tropoelastin b in containing a higher percentage of polar amino acids and cysteine residues. In addition, the amount of proline hydroxylation is 3 times higher than that found in chick tropoelastin b.

Amino Acids↗
PubMed1981

Optimal conditions for cell-free synthesis of elastin.

Optimal conditions for the translation of elastin mRNA1 in a mRNA-dependent rabbit reticulocyte lysate were determined. Using total RNA isolated from embryonic chick aortae as the source of exogenous RNA, the concentrations of various components present in the translation assay were varied and the effect on elastin synthesis quantitated by immunoprecipitation. Components examined included: magnesium acetate, potassium chloride, spermidine, creatine phosphate, ATP, and GTP. In addition, it was found that heating of the RNA prior to translation significantly enhanced total protein synthesis, elastin synthesis, and the synthesis of proteins possessing molecular weights of greater than 80,000.

Cell-Free System↗
PubMed1981

The biosynthesis of tropoelastin in chick and pig tissues.

The cell-free translation of elastin mRNA's from different tissues as well as different animal sources was investigated. In all cases elastin mRNA's coding for both tropoelastin a and b were found. Of special significance was the finding that the ratio of the two tropoelastins varied between lung and aortic tissues and this observation was consistent for two animal species.

Animals↗
PubMed1980

Comparison of aortic and ear cartilage tropoelastins isolated from lathyritic pigs.

Tropoelastin was isolated from aortae and auricular cartilage obtained from lathyritic piglets. The two tissue-specific tropoelastins were judged homogeneous by sodium dodecyl sulfate polyacrylamide gel electrophoresis and gel filtration on a high-pressure liquid chromatograph. Comparative studies of the tropoelastins were performed. Amino acid analysis revealed that the aortic and cartilage tropoelastins were very similar, if not identical, with the only exception that the cartilage tropoelastin contained more hydroxyproline and less lysine residues, both of which can be attributable to post-translational modifications. Both tropoelastins possess an apparent molecular weight of 70 000 and exhibit similar peptide fragments with limited trypsin cleavage. Antiserum raised to the aortic tropoelastin was used to show immunological identity between the two tissue tropoelastins.

Amino Acid Sequence↗