Kalaitzidis Demetrios, Neel Benjamin G
Hematology/Oncology-Cancer Biology Program, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
PLoS One. 2008;3(11):e3776. doi: 10.1371/journal.pone.0003776. Epub 2008 Nov 20.
Hematopoietic stem cells (HSCs) are probably the best-studied adult tissue-restricted stem cells. Although methods for flow cytometric detection of phosphoproteins in hematopoeitic progenitors and mature cells are available, analogous protocols for HSC are lacking. We present a robust method to study intracellular signaling in immunophenotypically-defined murine HSC/progenitor cell (HPC)-enriched populations. Using this method, we uncover differences in the response dynamics of several phosphoproteins representative of the Ras/MAP-Kinase(K), PI3K, mTOR and Jak/STAT pathways in HSC/HPCs stimulated by Scf, Thpo, as well as several other important HSC/HPC agonists.
造血干细胞(HSCs)可能是研究最为深入的成体组织限制性干细胞。尽管已有用于流式细胞术检测造血祖细胞和成熟细胞中磷酸化蛋白的方法,但缺乏针对造血干细胞的类似方案。我们提出了一种强大的方法,用于研究免疫表型定义的富含小鼠造血干细胞/祖细胞(HPC)群体中的细胞内信号传导。使用这种方法,我们发现了在干细胞因子(Scf)、血小板生成素(Thpo)以及其他几种重要的造血干细胞/祖细胞激动剂刺激下,造血干细胞/祖细胞中代表Ras/丝裂原活化蛋白激酶(MAPK)、磷脂酰肌醇-3激酶(PI3K)、雷帕霉素靶蛋白(mTOR)和Jak/信号转导子和转录激活子(STAT)途径的几种磷酸化蛋白的反应动力学差异。