Evidence of primary cilia in the developing rat heart.

Q2 Biochemistry, Genetics and Molecular Biology Cilia Pub Date : 2018-07-31 eCollection Date: 2018-01-01 DOI:10.1186/s13630-018-0058-z
Sarbjot Kaur, Sue R McGlashan, Marie-Louise Ward
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引用次数: 17

Abstract

Background: A transient increase in cytosolic Ca2+ (the "Ca2+ transient") determines the degree and duration of myocyte force development in the heart. However, we have previously observed that, under the same experimental conditions, the Ca2+ transients from isolated cardiac myocytes are reduced in amplitude in comparison to those from multicellular cardiac preparations. We therefore questioned whether the enzymatic cell isolation procedure might remove structures that modulate intracellular Ca2+ in some way. Primary cilia are found in a diverse range of cell types, and have an abundance of Ca2+-permeable membrane channels that result in Ca2+ influx when activated. Although primary cilia are reportedly ubiquitous, their presence and function in the heart remain controversial. If present, we hypothesized they might provide an additional Ca2+ entry pathway in multicellular cardiac tissue that was lost during cell isolation. The aim of our study was to look for evidence of primary cilia in isolated myocytes and ventricular tissue from rat hearts.

Methods: Immunohistochemical techniques were used to identify primary cilia-specific proteins in isolated myocytes from adult rat hearts, and in tissue sections from embryonic, neonatal, young, and adult rat hearts. Either mouse anti-acetylated α-tubulin or rabbit polyclonal ARL13B antibodies were used, counterstained with Hoechst dye. Selected sections were also labelled with markers for other cell types found in the heart and for myocyte F-actin.

Results: No evidence of primary cilia was found in either tissue sections or isolated myocytes from adult rat ventricles. However, primary cilia were present in tissue sections from embryonic, neonatal (P2) and young (P21 and P28) rat hearts.

Conclusion: The lack of primary cilia in adult rat hearts rules out their contribution to myocyte Ca2+ homoeostasis by providing a Ca2+ entry pathway. However, evidence of primary cilia in tissue from embryonic and very young rat hearts suggests they have a role during development.

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发育中的大鼠心脏中有初级纤毛的证据。
背景:细胞质Ca2+的短暂增加(“Ca2+瞬态”)决定了心肌细胞力发展的程度和持续时间。然而,我们之前观察到,在相同的实验条件下,与多细胞心脏制剂相比,来自分离心肌细胞的Ca2+瞬态的振幅降低。因此,我们质疑酶细胞分离程序是否可能以某种方式去除调节细胞内Ca2+的结构。初级纤毛存在于多种细胞类型中,并且具有丰富的Ca2+通透膜通道,当激活时导致Ca2+内流。虽然据报道初级纤毛无处不在,但它们在心脏中的存在和功能仍然存在争议。如果存在,我们假设它们可能在细胞分离过程中丢失的多细胞心脏组织中提供额外的Ca2+进入途径。我们研究的目的是寻找从大鼠心脏分离的心肌细胞和心室组织中原发纤毛的证据。方法:采用免疫组织化学技术鉴定成年大鼠心脏分离肌细胞以及胚胎、新生儿、幼鼠和成年大鼠心脏组织切片中的原代纤毛特异性蛋白。采用小鼠抗乙酰化α-微管蛋白或兔抗ARL13B多克隆抗体,用Hoechst染料反染。选定的切片也被标记为心脏中发现的其他细胞类型和心肌细胞f -肌动蛋白。结果:在成年大鼠脑室的组织切片和分离的肌细胞中均未发现原发性纤毛。然而,在胚胎、新生儿(P2)和幼龄(P21和P28)大鼠心脏的组织切片中存在初级纤毛。结论:成年大鼠心脏缺乏初级纤毛,通过提供Ca2+进入途径,排除了它们对心肌细胞Ca2+稳态的贡献。然而,在胚胎和非常年轻的大鼠心脏组织中发现的初级纤毛的证据表明,它们在发育过程中起着重要作用。
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来源期刊
Cilia
Cilia Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
6.40
自引率
0.00%
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0
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SF-Assemblin genes in Paramecium: phylogeny and phenotypes of RNAi silencing on the ciliary-striated rootlets and surface organization New software for automated cilia detection in cells (ACDC) Glioma cell proliferation is enhanced in the presence of tumor-derived cilia vesicles. Amyloid-β interrupts canonical Sonic hedgehog signaling by distorting primary cilia structure. Evidence of primary cilia in the developing rat heart.
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