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Merck

Estrogen Regulates the Satellite Cell Compartment in Females.

Cell reports (2019-07-11)
Brittany C Collins, Robert W Arpke, Alexie A Larson, Cory W Baumann, Ning Xie, Christine A Cabelka, Nardina L Nash, Hanna-Kaarina Juppi, Eija K Laakkonen, Sarianna Sipilä, Vuokko Kovanen, Espen E Spangenburg, Michael Kyba, Dawn A Lowe
要旨

Skeletal muscle mass, strength, and regenerative capacity decline with age, with many measures showing a greater deterioration in females around the time estrogen levels decrease at menopause. Here, we show that estrogen deficiency severely compromises the maintenance of muscle stem cells (i.e., satellite cells) as well as impairs self-renewal and differentiation into muscle fibers. Mechanistically, by hormone replacement, use of a selective estrogen-receptor modulator (bazedoxifene), and conditional estrogen receptor knockout, we implicate 17β-estradiol and satellite cell expression of estrogen receptor α and show that estrogen signaling through this receptor is necessary to prevent apoptosis of satellite cells. Early data from a biopsy study of women who transitioned from peri- to post-menopause are consistent with the loss of satellite cells coincident with the decline in estradiol in humans. Together, these results demonstrate an important role for estrogen in satellite cell maintenance and muscle regeneration in females.

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製品内容

Sigma-Aldrich
タモキシフェン, ≥99%
Sigma-Aldrich
2-メチルブタン, ReagentPlus®, ≥99%
Roche
In Situ細胞死検出キット、フルオレセイン, sufficient for ≤50 tests, suitable for detection
Sigma-Aldrich
抗ラミニン ウサギ宿主抗体, 0.5 mg/mL, affinity isolated antibody, buffered aqueous solution
Sigma-Aldrich
モノクロナール抗ラミニン マウス宿主抗体, clone LAM-89, purified from hybridoma cell culture