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在原代成骨细胞培养中骨组织样结构发育过程中,以单细胞分辨率检测细胞生长和骨特异性基因的表达。

Expression of cell growth and bone specific genes at single cell resolution during development of bone tissue-like organization in primary osteoblast cultures.

作者信息

Pockwinse S M, Wilming L G, Conlon D M, Stein G S, Lian J B

机构信息

Department of Cell Biology, University of Massachusetts Medical Center, Worcester 01655.

出版信息

J Cell Biochem. 1992 Jul;49(3):310-23. doi: 10.1002/jcb.240490315.

Abstract

Primary cultures of calvarial derived normal diploid osteoblasts undergo a developmental expression of genes reflecting growth, extracellular matrix maturation, and mineralization during development of multilayered nodules having a bone tissue-like organization. Scanning electron microscopy of the developing cultures indicates the transition from the uniform distribution of cuboidal osteoblasts to multilayered nodules of smaller cells with a pronounced orientation of perinodular cells towards the apex of the nodule. Ultrastructural analysis of the nodule by transmission electron microscopy indicates that the deposition of mineral is confined to the extracellular matrix where cells appear more osteocytic. The cell body contains rough endoplasmic reticulum and golgi, while these intracellular organelles are not present in the developing cellular processes. To understand the regulation of temporally expressed genes requires an understanding of which genes are selectively expressed on a single cell basis as the bone tissue-like organization develops. In situ hybridization analysis using 35S labelled histone gene probes, together with 3H-thymidine labelling and autoradiography, indicate that greater than 98% of the pre-confluent osteoblasts are proliferating. By two weeks, both the foci of multilayered cells and internodular cell regions have down-regulated cell growth associated genes. Post-proliferatively, but not earlier, initial expression of both osteocalcin and osteopontin are restricted to the multilayered nodules where all cells exhibit expression. While total mRNA levels for osteopontin and osteocalcin are coordinately upregulated with an increase in mineral deposition, in situ hybridization has revealed that expression of osteocalcin and osteopontin occurs predominantly in cells associated with the developing nodules. In contrast, proliferating rat osteosarcoma cells (ROS 17/2.8) concomitantly express histone H4, along with osteopontin and osteocalcin. These in situ analyses of gene expression during osteoblast growth and differentiation at the single cell level establish that a population of proliferating calvarial-derived cells subsequently expresses osteopontin and osteocalcin in cells developing into multilayered nodules with a tissue-like organization.

摘要

颅盖来源的正常二倍体成骨细胞的原代培养物在具有骨组织样结构的多层结节发育过程中经历反映生长、细胞外基质成熟和矿化的基因的发育性表达。对发育中的培养物进行扫描电子显微镜检查表明,从立方形成骨细胞的均匀分布转变为较小细胞的多层结节,结节周围细胞明显朝向结节顶端定向排列。通过透射电子显微镜对结节进行超微结构分析表明,矿物质沉积局限于细胞外基质,此处细胞更像骨细胞。细胞体含有粗面内质网和高尔基体,而这些细胞内细胞器在发育中的细胞突起中不存在。要了解时间表达基因的调控,需要了解在骨组织样结构发育过程中哪些基因在单个细胞基础上被选择性表达。使用35S标记的组蛋白基因探针进行原位杂交分析,结合3H-胸腺嘧啶标记和放射自显影,表明超过98%的汇合前成骨细胞在增殖。到两周时,多层细胞灶和结节间细胞区域都下调了与细胞生长相关的基因。增殖后但不是更早,骨钙素和骨桥蛋白的初始表达仅限于所有细胞都表达的多层结节。虽然骨桥蛋白和骨钙素的总mRNA水平随着矿物质沉积的增加而协同上调,但原位杂交显示骨钙素和骨桥蛋白的表达主要发生在与发育中的结节相关的细胞中。相比之下,增殖的大鼠骨肉瘤细胞(ROS 17/2.8)同时表达组蛋白H4以及骨桥蛋白和骨钙素。这些在成骨细胞生长和分化过程中在单细胞水平上对基因表达的原位分析表明,一群增殖的颅盖来源细胞随后在发育成具有组织样结构的多层结节的细胞中表达骨桥蛋白和骨钙素。

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