scholarly journals Myotome adaptability confers developmental robustness to somitic myogenesis in response to fibre number alteration

2017 ◽  
Vol 431 (2) ◽  
pp. 321-335 ◽  
Author(s):  
Shukolpa D. Roy ◽  
Victoria C. Williams ◽  
Tapan G. Pipalia ◽  
Kuoyu Li ◽  
Christina L. Hammond ◽  
...  
Keyword(s):  
Fibre Number

scholarly journals Early life undernutrition in rats

1982 ◽  
Vol 47 (3) ◽  
pp. 417-431 ◽  
Author(s):  
K. S. Bedi ◽  
A. R. Birzgalis ◽  
M. Mahon ◽  
J. L. Smart ◽  
A. C. Wareham
Keyword(s):  
Body Weight ◽  
Relative Frequency ◽  
Cross Sectional Area ◽  
Fibre Types ◽  
Male Rats ◽  
Sectional Area ◽  
Muscle Weight ◽  
Cross Sectional ◽  
Volume Proportion ◽  
Fibre Number

1. Male rats were undernourished either during the geslational and suckling periods or for a period of time immediately following weaning. Some rats were killed at the end of the period of undernutrition; others were nutritionally rehabilitated for lengthy periods of time before examination. Two muscles, the extensor digitorum longus (EDL) and soleus (SOL) were studied from each rat. Histochemically-stained transverse sections of these muscles were used to determine total number of fibres, the fibre cross-sectional areas and the relative frequency of the various fibre types.2. All rats killed immediately following undernutrition showed significant deficit sin body-weight, muscle weight and fibre cross-sectional area compared to age-matched controls.3. Animals undernourished during gestation and suckling and then fed normally for 5 months showed persistent and significant deficits in body-weight, muscle weight and total fibre number. There were also significant deficits in mean fibre cross-sectional area of each fibre type except for red fibres in the EDL. No difference in the volume proportion of connective tissue was found.4. Rats undernourished after weaning and then fed ad lib. for approximately 7 months had normal body-and muscle weights. Their muscles showed no significant differences in total fibre number, relative frequency of the various fibre types, fibre size or volume proportion of connective lissue.5. These results indicate that, although the effects on rat skeletal muscle of a period of undernutrition after weaning can be rectified, undernutrition before weaning causes lasting deficits.

scholarly journals Selection for Fibre Number in Merino Sheep

Nature ◽  
1956 ◽  
Vol 178 (4528) ◽  
pp. 330-330
Author(s):  
HELEN NEWTON TURNER
Keyword(s):  
Merino Sheep ◽  
Fibre Number ◽  
Selection For

Sources of variation in myofibre number within and between litters of pigs

1991 ◽  
Vol 52 (3) ◽  
pp. 527-533 ◽  
Author(s):  
C. M. Dwyer ◽  
N. C. Stickland
Keyword(s):  
Muscle Fibre ◽  
Significant Contribution ◽  
Large White ◽  
Significant Difference ◽  
Fresh Frozen ◽  
Sources Of Variation ◽  
Fibre Number ◽  
Acid Stable ◽  
Total Muscle ◽  
Secondary Fibre

ABSTRACTA study of the determinants of inter- and intra-litter variation in muscle fibre number was carried out on five litters of Large White piglets. Fresh frozen, whole mid-belly sections of m. semitendinosus were stained to demonstrate acid-stable myosin adenosine triphosphatase activity. From these sections it was possible to identify which fibres had developed as primary and which as secondary fibres. Estimations of total muscle fibre number, total primary fibre number and ratio of secondary fibres to primary fibres were made for each animal. Results demonstrated that primary fibre number varied between litters (P<0·01) and was responsible for the variation in total muscle fibre number (P < 005) between litters since there was no significant variation in secondary: primary ratio. Within-litter differences in total fibre number could be attributed to both the secondary: primary ratio and primary fibre number, in almost equal contributions. However, when only the largest and smallest extremes of the litters were compared, variation in fibre number was due to the significant difference in the secondary: primary ratio (P<0·01). Taken as a whole, the results appear to show that primary fibre number is responsible for all the variation in muscle fibre number between litters, and also makes a significant contribution, with secondary: primary fibre ratio, to the variation present within a litter. The factors responsible for variations in primary and secondary fibre numbers are discussed.

Angiotensin II can directly induce mitochondrial dysfunction, decrease oxidative fibre number and induce atrophy in mouse hindlimb skeletal muscle

2015 ◽  
Vol 100 (3) ◽  
pp. 312-322 ◽  
Author(s):  
Tomoyasu Kadoguchi ◽  
Shintaro Kinugawa ◽  
Shingo Takada ◽  
Arata Fukushima ◽  
Takaaki Furihata ◽  
...  
Keyword(s):  
Skeletal Muscle ◽  
Angiotensin Ii ◽  
Mitochondrial Dysfunction ◽  
Fibre Number

A note on fibre number and diameter in muscles of large and small lines of mice compared at a fixed body weight

1976 ◽  
Vol 22 (1) ◽  
pp. 131-133 ◽  
Author(s):  
A. C. B. Hooper ◽  
J. C. McCarthy
Keyword(s):  
Body Weight ◽  
Tibialis Anterior ◽  
Biceps Brachii ◽  
Control Population ◽  
High Line ◽  
Fibre Number

SummaryM. biceps brachii and m. tibialis anterior were studied at a fixed body weight in mice selected for high and low body weight at a fixed age. Muscle weights were approximately equal in the two lines. In general, muscles from high-line mice appeared to contain a larger number of smaller fibres than low-line mice in which there were fewer but wider fibres than in the unselected control population from which the lines were derived.

scholarly journals Multiscale molecular profiling of pathological bone resolves sexually dimorphic control of extracellular matrix composition

2021 ◽  
Vol 14 (3) ◽  
pp. dmm048116 ◽  
Author(s):  
Aikta Sharma ◽  
Alice Goring ◽  
Peter B. Johnson ◽  
Roger J. H. Emery ◽  
Eric Hesse ◽  
...  
Keyword(s):  
Extracellular Matrix ◽  
Ex Vivo ◽  
Second Harmonic ◽  
Collagen Fibre ◽  
Matrix Composition ◽  
Label Free ◽  
Fibre Number ◽  
Backscattered Electron ◽  
Matrix Mineralisation

ABSTRACTCollagen assembly during development is essential for successful matrix mineralisation, which determines bone quality and mechanocompetence. However, the biochemical and structural perturbations that drive pathological skeletal collagen configuration remain unclear. Deletion of vascular endothelial growth factor (VEGF; also known as VEGFA) in bone-forming osteoblasts (OBs) induces sex-specific alterations in extracellular matrix (ECM) conformation and mineralisation coupled to vascular changes, which are augmented in males. Whether this phenotypic dimorphism arises as a result of the divergent control of ECM composition and its subsequent arrangement is unknown and is the focus of this study. Herein, we used murine osteocalcin-specific Vegf knockout (OcnVEGFKO) and performed ex vivo multiscale analysis at the tibiofibular junction of both sexes. Label-free and non-destructive polarisation-resolved second-harmonic generation (p-SHG) microscopy revealed a reduction in collagen fibre number in males following the loss of VEGF, complemented by observable defects in matrix organisation by backscattered electron scanning electron microscopy. This was accompanied by localised divergence in collagen orientation, determined by p-SHG anisotropy measurements, as a result of OcnVEGFKO. Raman spectroscopy confirmed that the effect on collagen was linked to molecular dimorphic VEGF effects on collagen-specific proline and hydroxyproline, and collagen intra-strand stability, in addition to matrix carbonation and mineralisation. Vegf deletion in male and female murine OB cultures in vitro further highlighted divergence in genes regulating local ECM structure, including Adamts2, Spp1, Mmp9 and Lama1. Our results demonstrate the utility of macromolecular imaging and spectroscopic modalities for the detection of collagen arrangement and ECM composition in pathological bone. Linking the sex-specific genetic regulators to matrix signatures could be important for treatment of dimorphic bone disorders that clinically manifest in pathological nano- and macro-level disorganisation.This article has an associated First Person interview with the first author of the paper.

Vital statistics for an experimental flock of Merino sheep. III. Factors affecting wool and body characteristics, including the effect of age of ewe and its possible interaction with method of selection

1966 ◽  
Vol 17 (4) ◽  
pp. 557 ◽  
Author(s):  
GH Brown ◽  
HN Turner ◽  
SSY Young ◽  
CHS Dolling
Keyword(s):  
Body Weight ◽  
Fibre Diameter ◽  
Vital Statistics ◽  
Fibre Volume ◽  
Age Changes ◽  
Factors Affecting ◽  
Fibre Number ◽  
The Mean ◽  
Selection For ◽  
Staple Length

Estimates were made of the effects of the following factors on 10 fleece and body characteristics measured on breeding ewes aged 1½ to 10½ years in three mating groups over a period of 15 years: age of ewe, single or twin birth, age of dam, the ewe's own lambing performance, the year in which measurements were made, and the year in which each set of ewes was born. Two groups (S and MS) were under selection for high clean wool weight at 15–16 months, with a ceiling on wrinkle score and fibre diameter, while the third (C) was a random control. Changes with age were present in all characteristics and were similar in the three groups. The finding that selection on wool weight at an early age had no effect on subsequent age changes in any characteristic is of considerable importance. Greasy and clean wool weight reached a maximum at 34 years, then declined by 0.3–0.2 1b per year. Percentage clean yield, fibre diameter, body weight, and wrinkle score had maxima at 5½ to 6½ years. Staple length fell consistently by approximately 0.2 cm per year, while face cover rose consistently but slightly. Crimp number rose, fell, and rose again, while fibre number rose, fell, and remained constant from 4½ years. The chief source of increase in wool weight from l½ to 3½ years was an increase in the total number of fibres. The chief source of the subsequent fall was a decrease in fibre volume, with a minor contribution from a fall in total fibre number after 6½ years. Twin-born ewes cut 0.21 lb (4.2% of the mean) less clean wool per year over their lifetime than single-born ewes, while the progeny of 2-year-old ewes cut 0.32 lb (6.4%) less than the progeny of adults. The main source of lower weight in each case was a lower total fibre number. Pregnancy lowered clean wool weight more than lactation, the separate effects being 0.87 and 0.38 lb respectively (17.4 and 7.7% of the mean) and the combined effect 1.25 1b or 25.1%. Pregnancy lowered total fibre number but lactation had no further effect. Mean clean wool weights over all ages in the C group varied from year to year, the range being from 1.08 lb (21.6%)below the mean to 0.97 lb (19.4%) above. Differences in total fibre number contributed between one-third and two-thirds of the variation. Ewes born in consecutive years in the S and MS groups showed marked upward trends in clean wool weight, fibre number, and staple length, with a marked downward trend in crimp number and a slight upward trend in body weight. These trends demonstrate direct and correlated responses to the strong selection for high clean wool weight at 15–16 months of age, and the associated slight selection against fibre diameter and wrinkle score. The mean annual increases in clean wool weight were 0.15 and 0.11 Ib (3.0 and 2.2%) in the S and MS groups, approximately 40% of the increase arising from increased total fibre number and 40% from increased staple length. The effects of age and lambing performance can be used to predict productivity in flocks of differing age structures. As the casting age rises to 54 years changes in productivity are negligible. With a rise in casting age to 7½ years the average clean wool weight of the flock would fall by 0.14 lb, with a slight decrease in staple length and crimp number. These changes need to be balanced against any increased lambing percentage or decreased annual genetic gain due to increased generation interval. Comparison with other available figures indicates that age changes may vary from one area to another.

TEMPERATURE AND MYOGENIC FACTOR TRANSCRIPT LEVELS DURING EARLY DEVELOPMENT DETERMINES MUSCLE GROWTH POTENTIAL IN RAINBOW TROUT(ONCORHYNCHUS MYKISS) AND SEA BASS (DICENTRARCHUS LABRAX)

2001 ◽  
Vol 204 (16) ◽  
pp. 2763-2771 ◽  
Author(s):  
D. WILKES ◽  
S. Q. XIE ◽  
N. C. STICKLAND ◽  
H. ALAMI-DURANTE ◽  
M. KENTOURI ◽  
...  
Keyword(s):  
Rainbow Trout ◽  
Muscle Fibre ◽  
Early Development ◽  
Sea Bass ◽  
Growth Potential ◽  
Mrna Levels ◽  
European Sea Bass ◽  
Transcript Levels ◽  
Fibre Number ◽  
Sea Bass Larvae

SUMMARY The influence of changes in environmental temperature on the mRNA levels of myogenic regulatory factors (MRFs), i.e. MyoD and myogenin, as well as myosin heavy chain (MyHC) were studied during early larval development in rainbow trout and sea bass. Phosphoimager analysis of northern blots indicated that there is an optimum temperature for the RNA transcript levels of MRF and MyHC RNA in trout and in sea bass larvae. In the trout strain studied, the highest concentration for MRF and MyHC transcripts was found at 8°C rather than 4°C or 20°C. In European sea bass, the highest concentrations of MRF and MyHC mRNA were observed at 15-20°C rather than 13°C. Raising sea bass larvae at 15°C was associated with higher MyHC gene expression as well as a trend towards an increase in total muscle fibre number and higher growth rates after transfer at ambient temperature. Results suggest that mRNA levels of MRF and MyHC can be used to optimise early development. An experiment in which the temperature was changed illustrates the consequence of precise temporal expression of MRF genes in specifying muscle fibre number at critical stages during early development.

Effects of inbreeding on four families of Peppin Merinos

1957 ◽  
Vol 8 (3) ◽  
pp. 299 ◽  
Author(s):  
JM Doney
Keyword(s):  
Fibre Diameter ◽  
Genetic Effect ◽  
Direct Consequence ◽  
Specific Gene ◽  
Single Strain ◽  
Merino Sheep ◽  
Fibre Number ◽  
Per Se ◽  
Fleece Weight ◽  
Australian Merino

The influence of inbreeding on several fleece and body characters in a strain of Australian Merino sheep is reported. The four families from which data were taken were derived from a single strain of Peppin Merinos. Inbreeding without selection has been carried on since the foundation of the families between 1939 and 1944. Inbreeding is responsible for a reduction in body size, fertility, greasy and clean fleece weight, and wrinkle score, but has relatively little influence on the fleece components (yield, staple length, fibre diameter, and density of fibre population). It follows that the reduction in fleece weight is a direct consequence of a decrease in total fibre number. Since the reduction in fibre number is likely to be a correlated effect of low pre-natal and early post-natal growth rates, it is suggested that the inbreeding has had no genetic effect on the several independent systems involved in adult wool production but has affected only those associated with fitness and vigour. The depression due to inbreeding therefore may not be caused by specific gene fixation but by increased homozygosity per se.

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