Cyclin D3 Colocalizes with Myogenin and p21 in Skeletal Muscle Satellite Cells during Early-Stage Functional Overload

IF 1.6 4区 生物学 Q4 CELL BIOLOGY
Minenori Ishido
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引用次数: 0

Abstract

Myogenic cell differentiation is modulated by multiple regulatory factors, such as myogenin, p21, and cyclin D3 during myogenesis in vitro. It is also recognized that myogenin and p21 play important roles in regulating muscle satellite cell (SC) differentiation during overload-induced muscle hypertrophy in vivo. However, the expression patterns and functional role of cyclin D3 in the progress of muscle hypertrophy remain unclear. Thus, the present study investigated cyclin D3 expression in skeletal muscles during early-stage functional overload. Plantaris muscles were exposed to functional overload due to ablation of the gastrocnemius and soleus muscles. As a result, cyclin D3 expression was detected in the nuclei of SCs but not in myonuclei on day 1 after surgery. Cyclin D3 expression, after functional overload, gradually increased, reaching a maximum on day 7 along with myogenin expression. Moreover, in response to the functional overload, cyclin D3 was expressed simultaneously with myogenin and p21 in SC nuclei. Therefore, the present study suggests that cyclin D3 with myogenin and p21 may interactively regulate SC differentiation during early-stage functional overload.

早期功能超负荷时骨骼肌卫星细胞中的细胞周期蛋白 D3 与肌原蛋白和 p21 共定位
在体外肌生成过程中,肌原蛋白、p21 和细胞周期蛋白 D3 等多种调节因子可调节肌原细胞的分化。人们还认识到,在体内超负荷诱导的肌肉肥大过程中,肌原蛋白和 p21 在调节肌肉卫星细胞(SC)分化方面发挥着重要作用。然而,细胞周期蛋白 D3 在肌肉肥大过程中的表达模式和功能作用仍不清楚。因此,本研究调查了早期功能性超负荷时骨骼肌中细胞周期蛋白 D3 的表达。由于腓肠肌和比目鱼肌被消融,跖肌暴露于功能性超负荷。结果,在术后第1天,在SC细胞核中检测到了细胞周期蛋白D3的表达,而在肌核中却没有检测到。功能性超负荷后,细胞周期蛋白 D3 的表达逐渐增加,在第 7 天与肌原蛋白的表达一起达到最大值。此外,在功能超负荷后,细胞周期蛋白 D3 与肌原蛋白和 p21 同时在 SC 细胞核中表达。因此,本研究表明,细胞周期蛋白D3与肌原蛋白和p21可能在功能超负荷早期阶段相互作用,调控SC的分化。
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来源期刊
Acta Histochemica Et Cytochemica
Acta Histochemica Et Cytochemica 生物-细胞生物学
CiteScore
3.50
自引率
8.30%
发文量
17
审稿时长
>12 weeks
期刊介绍: Acta Histochemica et Cytochemica is the official online journal of the Japan Society of Histochemistry and Cytochemistry. It is intended primarily for rapid publication of concise, original articles in the fields of histochemistry and cytochemistry. Manuscripts oriented towards methodological subjects that contain significant technical advances in these fields are also welcome. Manuscripts in English are accepted from investigators in any country, whether or not they are members of the Japan Society of Histochemistry and Cytochemistry. Manuscripts should be original work that has not been previously published and is not being considered for publication elsewhere, with the exception of abstracts. Manuscripts with essentially the same content as a paper that has been published or accepted, or is under consideration for publication, will not be considered. All submitted papers will be peer-reviewed by at least two referees selected by an appropriate Associate Editor. Acceptance is based on scientific significance, originality, and clarity. When required, a revised manuscript should be submitted within 3 months, otherwise it will be considered to be a new submission. The Editor-in-Chief will make all final decisions regarding acceptance.
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