Intercellular Signaling Pathways Active During Intervertebral Disc Growth, Differentiation, and Aging

医学 椎间盘 细胞内 细胞生物学 解剖 生物
作者
Chitra Lekha Dahia,Eric Mahoney,Atiq Durrani,Christopher Wylie
出处
期刊:Spine [Ovid Technologies (Wolters Kluwer)]
卷期号:34 (5): 456-462 被引量:54
标识
DOI:10.1097/brs.0b013e3181913e98
摘要

In Brief Study Design. Intervertebral discs at different postnatal ages were assessed for active intercellular signaling pathways. Objective. To generate a spatial and temporal map of the signaling pathways active in the postnatal intervertebral disc (IVD). Summary of Background Data. The postnatal IVD is a complex structure, consisting of 3 histologically distinct components, the nucleus pulposus, fibrous anulus fibrosus, and endplate. These differentiate and grow during the first 9 weeks of age in the mouse. Identification of the major signaling pathways active during and after the growth and differentiation period will allow functional analysis using mouse genetics and identify targets for therapy for individual components of the disc. Methods. Antibodies specific for individual cell signaling pathways were used on cryostat sections of IVD at different postnatal ages to identify which components of the IVD were responding to major classes of intercellular signal, including sonic hedgehog, Wnt, TGFβ, FGF, and BMPs. Results. We present a spatial/temporal map of these signaling pathways during growth, differentiation, and aging of the disc. Conclusion. During growth and differentiation of the disc, its different components respond at different times to different intercellular signaling ligands. Most of these are dramatically downregulated at the end of disc growth. This study describes the spatial and temporal expression of the major cell signaling pathways during postnatal differentiation and aging of the mouse intervertebral disc. During growth, differentiation, and aging, the different components of the disc respond at different times to different cell signaling ligands.

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Rainbow完成签到,获得积分10
刚刚
年华完成签到,获得积分10
刚刚
e394282438完成签到,获得积分10
刚刚
hi_zhanghao完成签到,获得积分10
1秒前
思源应助ldroc采纳,获得10
1秒前
旋疯小子发布了新的文献求助10
2秒前
黎明完成签到,获得积分10
2秒前
RDQ完成签到,获得积分10
3秒前
tingalan完成签到,获得积分10
3秒前
4秒前
以恒之心完成签到,获得积分10
5秒前
5秒前
Ava应助pcyang采纳,获得30
5秒前
桐桐应助τ涛采纳,获得10
6秒前
AURORA丶完成签到,获得积分10
6秒前
6秒前
wanghao完成签到 ,获得积分10
7秒前
xpd发布了新的文献求助30
7秒前
隐形曼青应助韩乐乐采纳,获得10
7秒前
贺兰鸵鸟完成签到,获得积分10
8秒前
完美世界应助黎明采纳,获得10
8秒前
zxs哈哈哈哈完成签到,获得积分10
8秒前
下课了吧完成签到,获得积分10
8秒前
陶醉聪展完成签到 ,获得积分10
9秒前
俭朴的发带完成签到,获得积分10
9秒前
sun完成签到,获得积分10
10秒前
杨xy完成签到,获得积分10
10秒前
yiyi发布了新的文献求助10
10秒前
未改完成签到,获得积分10
11秒前
郭储能完成签到,获得积分10
11秒前
一一完成签到,获得积分10
11秒前
优雅的怀莲完成签到,获得积分10
11秒前
西瓜橙子完成签到,获得积分10
11秒前
LX发布了新的文献求助10
11秒前
Noel应助不爱科研采纳,获得10
11秒前
扑火退羽完成签到,获得积分10
12秒前
伯努利完成签到,获得积分10
12秒前
13秒前
情怀应助旋疯小子采纳,获得10
13秒前
拾光完成签到,获得积分10
13秒前
高分求助中
Lire en communiste 1000
Ore genesis in the Zambian Copperbelt with particular reference to the northern sector of the Chambishi basin 800
Becoming: An Introduction to Jung's Concept of Individuation 600
Communist propaganda: a fact book, 1957-1958 500
Briefe aus Shanghai 1946‒1952 (Dokumente eines Kulturschocks) 500
A new species of Coccus (Homoptera: Coccoidea) from Malawi 500
A new species of Velataspis (Hemiptera Coccoidea Diaspididae) from tea in Assam 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3167325
求助须知:如何正确求助?哪些是违规求助? 2818822
关于积分的说明 7922729
捐赠科研通 2478613
什么是DOI,文献DOI怎么找? 1320412
科研通“疑难数据库(出版商)”最低求助积分说明 632776
版权声明 602443