Isolation of Mouse Megakaryocyte Progenitors

巨核细胞 祖细胞 生物 造血 细胞生物学 干细胞 单元格排序 免疫学 血小板生成素 骨髓 流式细胞术
作者
Quentin Kimmerlin,Manuela Tavian,Christian Gachet,François Lanza,Nathalie Brouard
出处
期刊:Journal of Visualized Experiments [MyJoVE Corporation]
卷期号: (171) 被引量:3
标识
DOI:10.3791/62498
摘要

Bone marrow megakaryocytes are large polyploid cells that ensure the production of blood platelets. They arise from hematopoietic stem cells through megakaryopoiesis. The final stages of this process are complex and classically involve the bipotent Megakaryocyte-Erythrocyte Progenitors (MEP) and the unipotent Megakaryocyte Progenitors (MKp). These populations precede the formation of bona fide megakaryocytes and, as such, their isolation and characterization could allow for the robust and unbiased analysis of megakaryocyte formation. This protocol presents in detail the procedure to collect hematopoietic cells from mouse bone marrow, the enrichment of hematopoietic progenitors through magnetic depletion and finally a cell sorting strategy that yield highly purified MEP and MKp populations. First, bone marrow cells are collected from the femur, the tibia, and also the iliac crest, a bone that contains a high number of hematopoietic progenitors. The use of iliac crest bones drastically increases the total cell number obtained per mouse and thus contributes to a more ethical use of animals. A magnetic lineage depletion was optimized using 450 nm magnetic beads allowing a very efficient cell sorting by flow cytometry. Finally, the protocol presents the labeling and gating strategy for the sorting of the two highly purified megakaryocyte progenitor populations: MEP (Lin-Sca-1-c-Kit+CD16/32-CD150+CD9dim) and MKp (Lin- Sca-1-c-Kit+CD16/32-CD150+CD9bright). This technique is easy to implement and provides enough cellular material to perform i) molecular characterization for a deeper knowledge of their identity and biology, ii) in vitro differentiation assays, that will provide a better understanding of the mechanisms of maturation of megakaryocytes, or iii) in vitro models of interaction with their microenvironment.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
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
hohn发布了新的文献求助10
刚刚
刚刚
激动的一手完成签到,获得积分10
1秒前
2秒前
英俊的铭应助tf采纳,获得10
3秒前
GiGi发布了新的文献求助10
3秒前
4秒前
欧小仙完成签到,获得积分10
4秒前
5秒前
呵呵禾完成签到,获得积分10
6秒前
大力魂幽发布了新的文献求助10
7秒前
wangayting发布了新的文献求助10
8秒前
8秒前
9秒前
9秒前
渊鱼应助科研通管家采纳,获得10
9秒前
渊鱼应助科研通管家采纳,获得10
9秒前
科研通AI6应助科研通管家采纳,获得10
9秒前
9秒前
科研通AI6应助科研通管家采纳,获得10
9秒前
852应助科研通管家采纳,获得10
9秒前
9秒前
852应助科研通管家采纳,获得10
9秒前
搜集达人应助科研通管家采纳,获得10
9秒前
9秒前
汉堡包应助阵雨采纳,获得10
9秒前
渊鱼应助科研通管家采纳,获得10
9秒前
NexusExplorer应助科研通管家采纳,获得10
9秒前
科研通AI2S应助科研通管家采纳,获得10
9秒前
隐形曼青应助科研通管家采纳,获得10
9秒前
脑洞疼应助科研通管家采纳,获得10
9秒前
英姑应助科研通管家采纳,获得10
9秒前
研友_VZG7GZ应助科研通管家采纳,获得10
9秒前
顾矜应助科研通管家采纳,获得10
9秒前
彭于晏应助科研通管家采纳,获得10
9秒前
10秒前
aqaqaqa发布了新的文献求助10
10秒前
11秒前
12秒前
量子星尘发布了新的文献求助30
12秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Introduction to strong mixing conditions volume 1-3 5000
Clinical Microbiology Procedures Handbook, Multi-Volume, 5th Edition 2000
从k到英国情人 1500
Ägyptische Geschichte der 21.–30. Dynastie 1100
„Semitische Wissenschaften“? 1100
Real World Research, 5th Edition 800
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5736834
求助须知:如何正确求助?哪些是违规求助? 5368742
关于积分的说明 15334181
捐赠科研通 4880593
什么是DOI,文献DOI怎么找? 2622909
邀请新用户注册赠送积分活动 1571817
关于科研通互助平台的介绍 1528640