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Restricted maternal nutrition alters myogenic regulatory factor expression in satellite cells of ovine offspring
J S Raja1, M L Hoffman1, K E Govoni1
1Department of Animal Science,University of Connecticut,3636 Horsebarn Rd Ext,Storrs, CT,USA.
Insights
Poor maternal nutrition negatively impacts offspring muscle growth by altering satellite cell development. Restricted gestation diets changed the timing of key muscle growth gene expression, potentially reducing muscle formation in lambs.
Area of Science:
- Muscle biology
- Developmental biology
- Nutritional science
Background:
- Maternal nutrition is crucial for fetal development, including muscle growth.
- Satellite cells are essential for postnatal muscle growth and repair.
- Myogenic regulatory factors (e.g., MyoD, myogenin) control satellite cell activity.
Purpose of the Study:
- To investigate the impact of maternal nutritional restriction during gestation on the temporal expression of MyoD and myogenin in offspring satellite cells.
- To assess how these changes affect satellite cell function and muscle growth potential.
Main Methods:
- Ewes were fed 100% or 60% of NRC requirements during gestation.
- Satellite cells were isolated from offspring at birth and 3 months of age.
- In vitro culture and gene expression analysis (immunostaining for Pax7, MyoD, myogenin) were performed.
Main Results:
- Maternal nutritional restriction altered the temporal expression of MyoD and myogenin in satellite cells at birth and 3 months.
- Increased MyoD and myogenin expression was observed in restricted offspring at specific time points.
- A reduced fusion index was noted in satellite cells from restricted offspring at 3 months of age.
Conclusions:
- Poor maternal nutrition during gestation disrupts the normal temporal expression of myogenic regulatory factors in offspring satellite cells.
- These alterations may lead to reduced myoblast proliferation and fusion, contributing to impaired postnatal muscle growth.
- This study highlights the long-term consequences of gestational nutrition on muscle development.
Abstract:
Poor maternal nutrition inhibits muscle development and postnatal muscle growth. Satellite cells are myogenic precursor cells that contribute to postnatal muscle growth, and their activity can be evaluated by the expression of several transcription factors. Paired-box (Pax)7 is expressed in quiescent and active satellite cells. MyoD is expressed in activated and proliferating satellite cells and myogenin is expressed in terminally differentiating cells. Disruption in the expression pattern or timing of expression of myogenic regulatory factors negatively affects muscle development and growth. We hypothesized that poor maternal nutrition during gestation would alter the in vitro temporal expression of MyoD and myogenin in satellite cells from offspring at birth and 3 months of age. Ewes were fed 100% or 60% of NRC requirements from day 31±1.3 of gestation. Lambs from control-fed (CON) or restricted-fed (RES) ewes were euthanized within 24 h of birth (birth; n=5) or were fed a control diet until 3 months of age (n=5). Satellite cells isolated from the semitendinosus muscle were used for gene expression analysis or cultured for 24, 48 or 72 h and immunostained for Pax7, MyoD or myogenin. Fusion index was calculated from a subset of cells allowed to differentiate. Compared with CON, temporal expression of MyoD and myogenin was altered in cultured satellite cells isolated from RES lambs at birth. The percent of cells expressing MyoD was greater in RES than CON (P=0.03) after 24 h in culture. After 48 h of culture, there was a greater percent of cells expressing myogenin in RES compared with CON (P0.05). In satellite cells from RES lambs at 3 months of age, the percent of cells expressing MyoD and myogenin were greater than CON after 72 h in culture (P<0.05). Fusion index was reduced in RES lambs at 3 months of age compared with CON (P<0.001). Restricted nutrition during gestation alters the temporal expression of myogenic regulatory factors in satellite cells of the offspring, which may reduce the pool of myoblasts, decrease myoblast fusion and contribute to the poor postnatal muscle growth previously observed in these animals.
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