Limbkar Kedar, Dhenge Ankita, Jadhav Dipesh D, Thulasiram Hirekodathakallu V, Kale Vaijayanti, Limaye Lalita
National Centre for Cell Science, NCCS Complex, Savitribai Phule Pune University Campus, Pune 411007, India.
Chemical Biology Unit, Division of Organic Chemistry, CSIR- National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411008, India.
Data Brief. 2017 Aug 9;14:551-557. doi: 10.1016/j.dib.2017.08.009. eCollection 2017 Oct.
Stem cells have peculiar property to self-renew and differentiate. It is important to control their fate in safe and effective ways for their therapeutic use. The mediators of essential polyunsaturated fatty acids (PUFAs) namely Arachidonic acid (AA) and Docosahexanoic acid (DHA) are known to play a role in haematopoiesis via various metabolic pathways [1]. However the direct effect of purified AA or DHA on haematopoiesis has not been well investigated yet. We have reported that oral administration of PUFAs enhanced haematopoiesis in mice [2]. Signaling Leukocyte Antigen Molecule (SLAM) (CD48CD150) phenotype consists of pure population of haematopoietic stem cells (HSCs). Herein we observed higher percentage of SLAM (CD48CD150) phenotype in the bone marrow (BM) cells of mice fed with AA or DHA compared to PBS fed control mice. Data from engraftment study depicts that BM from AA/DHA-fed mice showed higher absolute number of donor cells in recipient mice compared to control. The enhanced hematopoiesis observed in AA/DHA-fed mice was returned to normal when the mice were kept on normal diet for six weeks (after ten days of oral feeding). We confirmed GCMS (Gas Chromatography-Mass Spectroscopy) retention times of AA and DHA by co-injecting fatty acid extract from AA or DHA fed mice with purified AA or DHA standards respectively. Representative flow cytometry profile of LinSca-1c-kit(LSK) cells showed higher expression of CXCR4 protein and ligands of Wnt, Notch1 signaling in BM of AA/DHA-fed mice.
干细胞具有自我更新和分化的独特特性。以安全有效的方式控制它们的命运对于其治疗应用至关重要。已知必需多不饱和脂肪酸(PUFA)的介质,即花生四烯酸(AA)和二十二碳六烯酸(DHA),通过各种代谢途径在造血过程中发挥作用[1]。然而,纯化的AA或DHA对造血的直接影响尚未得到充分研究。我们已经报道口服PUFA可增强小鼠的造血功能[2]。信号淋巴细胞抗原分子(SLAM)(CD48CD150)表型由纯的造血干细胞(HSC)群体组成。在此,我们观察到与喂食PBS的对照小鼠相比,喂食AA或DHA的小鼠骨髓(BM)细胞中SLAM(CD48CD150)表型的百分比更高。移植研究的数据表明,与对照相比,来自喂食AA/DHA小鼠的BM在受体小鼠中显示出更高的供体细胞绝对数量。当小鼠在正常饮食六周后(口服喂养十天后),在喂食AA/DHA的小鼠中观察到的增强的造血功能恢复正常。我们通过分别将来自喂食AA或DHA小鼠的脂肪酸提取物与纯化的AA或DHA标准品共注射,确认了AA和DHA的气相色谱-质谱(GCMS)保留时间。代表性的LinSca-1c-kit(LSK)细胞流式细胞术图谱显示,在喂食AA/DHA的小鼠骨髓中,CXCR4蛋白以及Wnt、Notch1信号配体的表达更高。