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原发性髓系细胞蛋白质组学和转录组学:β-微管蛋白异构体对破骨细胞功能的重要性。

Primary myeloid cell proteomics and transcriptomics: importance of β-tubulin isotypes for osteoclast function.

机构信息

Centre de Recherche de Biologie Cellulaire de Montpellier (CRBM), Montpellier Univ., CNRS, 34000 Montpellier, France.

Institut de Pharmacologie et Biologie Structurale, IPBS, Université de Toulouse, CNRS, UPS, 31077 Toulouse Cedex 04, France.

出版信息

J Cell Sci. 2020 May 27;133(10):jcs239772. doi: 10.1242/jcs.239772.

Abstract

Among hematopoietic cells, osteoclasts (OCs) and immature dendritic cells (DCs) are closely related myeloid cells with distinct functions: OCs participate skeleton maintenance while DCs sample the environment for foreign antigens. Such specificities rely on profound modifications of gene and protein expression during OC and DC differentiation. We provide global proteomic and transcriptomic analyses of primary mouse OCs and DCs, based on original stable isotope labeling with amino acids in cell culture (SILAC) and RNAseq data. We established specific signatures for OCs and DCs, including genes and proteins of unknown functions. In particular, we showed that OCs and DCs have the same α- and β-tubulin isotype repertoire but that OCs express much more of the β tubulin isotype Tubb6 (also known as TBB6). In both mouse and human OCs, we demonstrate that elevated expression of Tubb6 in OCs is necessary for correct podosomes organization and thus for the structure of the sealing zone, which sustains the bone resorption apparatus. Hence, lowering Tubb6 expression hinders OC resorption activity. Overall, we highlight here potential new regulators of OC and DC biology, and illustrate the functional importance of the tubulin isotype repertoire in the biology of differentiated cells.

摘要

在造血细胞中,破骨细胞 (OCs) 和未成熟树突状细胞 (DCs) 是密切相关的髓系细胞,具有不同的功能:OCs 参与骨骼维护,而 DCs 则对外来抗原进行环境采样。这种特异性依赖于 OC 和 DC 分化过程中基因和蛋白质表达的深刻修饰。我们基于原始的稳定同位素标记与细胞培养中的氨基酸 (SILAC) 和 RNAseq 数据,对原代小鼠 OCs 和 DCs 进行了全面的蛋白质组学和转录组学分析。我们为 OCs 和 DCs 建立了特定的特征,包括具有未知功能的基因和蛋白质。特别是,我们表明 OCs 和 DCs 具有相同的α-和β-微管蛋白同工型,但 OCs 表达更多的β微管蛋白同工型 Tubb6(也称为 TBB6)。在人和小鼠的 OCs 中,我们证明了 Tubb6 在 OCs 中的高表达对于正确的足突组织和密封区的结构是必要的,这维持了骨吸收装置。因此,降低 Tubb6 的表达会阻碍 OC 的吸收活性。总的来说,我们在这里强调了潜在的 OC 和 DC 生物学新调节剂,并说明了微管蛋白同工型在分化细胞生物学中的功能重要性。

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