Fiber type characteristics and myosin light chain expression in a world champion shot putter.

Muscle biopsies from m. vastus lateralis of two world class shot putters (shot putter 1 and 2) and the untrained brother of shot putter 1 were analyzed for fiber type distribution with ATPase staining and in situ hybridization for the expression of alkali myosin light chain (MLC) isoforms. Shot putter 2 had a predominance of type II fibers (67 X) and distinct hypertrophy of type I as well as type II fibers (fiber areas of 5939 and 8531 microm2). In shot putter 1, type II fibers amounted to only 40%, due to their selective hypertrophy, however type II fibers (10265 microm2) accounted for 67 2% of the total cross-sectional area. The type I fibers in shot putter 1 were similar in size to his untrained brother (3430 vs 3790 microm2). After 3 years of active detraining, type II fibers of shot putter 1 had reduced in size to values closer to those of his brother (7746 and 6340 microm2). The large difference between type I and type II fiber size, even in the untrained state, in both shot putter 1 and his brother is not usually seen in humans and maybe a genetic characteristic. We suggest that the ability to selectively increase the relative area of his type II fibers in the 15 years of strength training was a key element in his success as a shot putter. The observed increase in the expression of fast myosin light chain mRNAs in both fiber types is indicative of further adjustment of the myofibrillar apparatus towards the generation of very high peak power.

Intima-like smooth muscle cells: developmental link between endothelium and media?

The presence of non-contractile smooth muscle cells within the arterial wall raises questions as to their origin and function. These cells abound within the aortae of murine and porcine neonates, but are also present within the intimal and medial layers of adult arteries. They are largely devoid of smooth muscle-associated proteins and manifest an epithelioid form. Their morphological resemblance to endothelial cells prompted us to explore this potential relationship and to investigate their angiogenic properties in three-dimensional collagen gels. Using well-characterized smooth muscle cell lines, displaying either the intima-like (epithelioid) or media-like (spindle-shaped) morphology, we were able to show that intima-like cells share several features in common with endothelial ones and can transform into a media-like phenotype, whereby they irreversibly lose their characteristic pattern of protein expression. Intima-like, but not media-like, vascular smooth muscle cells are capable of forming capillary tubes, and, in co-cultures, can induce media-like ones to participate in this process. Such capillaries consist of a randomly-organized, mixed population of endothelial cells with intima-like or media-like smooth muscle ones. The functional significance of this diversity in smooth muscle cell type is not well understood, but phenotypic plasticity could conceivably figure as an important adaptive response to changes in the local environment.

Fibre-type specific expression of fast and slow essential myosin light chain mRNAs in trained human skeletal muscles.

The fibre-type specific expression patterns of fast and slow isoforms of essential (alkali) myosin light chains (ELC) was analysed in trained, untrained and pathological human muscles. Biopsies from m. vastus lateralis of moderately trained and untrained persons, as well as highly trained endurance and strength athletes were analysed, by in situ hybridization, for the expression of the 'fast' ELC 1f/3f and the 'slow' ELC 1 sb. We wanted to investigate if changes in the fibre-type specific ELC mRNA pattern could be used as markers for training adaptation, especially, if the mRNA of the slow ELC 1sb isoform would appear in type IIA fibres as a result of endurance training (Baumann et al. 1987). We found the fast/slow ELC expression patterns in the fibre types to be remarkably stable. Physiological stress, even high training loads, did not affect it. No IIA fibres expressing ELC 1sb mRNA were found. They could be detected, however, in pathological muscle samples, where fast/slow ELC patterns not found in normal muscles were frequent. Our data suggest that in healthy muscles, only a subset of the theoretically possible combinations of myosin heavy and light chain isoforms are expressed at the level of their mRNAs.

Expression of smooth muscle markers in the developing murine lung: potential contractile properties and lineal descent.

Contractile cells in the mammalian lung develop in close association with the outgrowing stem bronchi. Fully differentiated smooth muscle cells are typically found in proximal regions, residing in the substantial muscular walls of the major airways and blood vessels. More distally, cells expressing markers of differentiated smooth muscle cells to a variable degree, and which may therefore possess contractile properties, are to be found scattered around the interstitium. We have investigated the temporal and spatial distribution of smooth muscle lineage markers (smooth muscle myosin mRNA) and of those indicative of contractile function (metavinculin mRNA) in the murine lung. In the smooth muscle layers of the bronchi and major blood vessels, these genes are expressed from the onset of pulmonary budding, concurrently with the appearance of alpha-smooth muscle actin and calponin proteins. During fetal development, smooth muscle-associated genes and proteins are restricted to this committed smooth muscle population. The first signs of myofibroblast or pericyte differentiation become manifest perinatally, when their expression of alpha-smooth muscle actin escalates. In the adult lung, such cells may be readily pin-pointed by their positive reaction for metavinculin mRNA, but, at maturity, they do not always coexpress alpha-smooth muscle actin.