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生长激素治疗对生长激素缺乏症儿童CD34+造血细胞凋亡评估的影响

The Impact of Growth Hormone Therapy on the Apoptosis Assessment in CD34+ Hematopoietic Cells from Children with Growth Hormone Deficiency.

作者信息

Kawa Miłosz Piotr, Stecewicz Iwona, Piecyk Katarzyna, Paczkowska Edyta, Rogińska Dorota, Sobuś Anna, Łuczkowska Karolina, Pius-Sadowska Ewa, Gawrych Elżbieta, Petriczko Elżbieta, Walczak Mieczysław, Machaliński Bogusław

机构信息

Department of General Pathology, Pomeranian Medical University in Szczecin, 72 Powstancow Wlkp. Street, 70-111 Szczecin, Poland.

Department of Pediatrics, Endocrinology, Diabetology, Metabolic Diseases and Cardiology of the Developmental Age, Pomeranian Medical University in Szczecin, 1 Unii Lubelskiej Street, 71-252 Szczecin, Poland.

出版信息

Int J Mol Sci. 2017 Jan 7;18(1):111. doi: 10.3390/ijms18010111.

Abstract

Growth hormone (GH) modulates hematopoietic cell homeostasis and is associated with apoptosis control, but with limited mechanistic insights. Aim of the study was to determine whether GH therapeutic supplementation (GH-TS) could affect apoptosis of CD34+ cells enriched in hematopoietic progenitor cells of GH deficient (GHD) children. CD34+ cells from peripheral blood of 40 GHD children were collected before and in 3rd and 6th month of GH-TS and compared to 60 controls adjusted for bone age, sex, and pubertal development. Next, apoptosis assessment via different molecular techniques was performed. Finally, to comprehensively characterize apoptosis process, global gene expression profile was determined using genome-wide RNA microarray technology. Results showed that GH-TS significantly reduced spontaneous apoptosis in CD34+ cells ( < 0.01) and results obtained using different methods to detect early and late apoptosis in analyzed cells population were consistent. GH-TS was also associated with significant downregulation of several members of TNF-alpha superfamily and other genes associated with apoptosis and stress response. Moreover, the significant overexpression of cyto-protective and cell cycle-associated genes was detected. These findings suggest that recombinant human GH has a direct anti-apoptotic activity in hematopoietic CD34+ cells derived from GHD subjects in course of GH-TS.

摘要

生长激素(GH)调节造血细胞稳态,并与细胞凋亡控制相关,但相关机制的研究尚有限。本研究旨在确定生长激素治疗性补充(GH-TS)是否会影响生长激素缺乏(GHD)儿童造血祖细胞中富集的CD34+细胞的凋亡。收集40例GHD儿童外周血中的CD34+细胞,分别在GH-TS治疗前、治疗第3个月和第6个月采集,并与60例根据骨龄、性别和青春期发育进行匹配的对照进行比较。接下来,通过不同分子技术进行细胞凋亡评估。最后,为全面表征细胞凋亡过程,使用全基因组RNA微阵列技术测定整体基因表达谱。结果显示,GH-TS显著降低了CD34+细胞的自发凋亡(<0.01),并且使用不同方法检测分析细胞群体中早期和晚期凋亡所获得的结果是一致的。GH-TS还与肿瘤坏死因子-α超家族的几个成员以及其他与细胞凋亡和应激反应相关的基因的显著下调有关。此外,还检测到细胞保护和细胞周期相关基因的显著过表达。这些发现表明,重组人生长激素在GH-TS过程中对源自GHD受试者的造血CD34+细胞具有直接的抗凋亡活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/747a/5297745/97b7df3d7ced/ijms-18-00111-g001.jpg

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