Morphology, differentiation and adhesion molecule expression changes of bone marrow mesenchymal stem cells from acute myeloid leukemia patients

被引:35
作者
Chen, Qiulei [1 ]
Yuan, Yan [1 ]
Chen, Tong [1 ]
机构
[1] Fudan Univ, Huashan Hosp, Dept Hematol, Shanghai 200040, Peoples R China
基金
中国国家自然科学基金;
关键词
acute myeloid leukemia; bone marrow mesenchymal stem cells; hematopoietic stem cell niche; adipogenic; osteogenic; adhesion molecule; N-CADHERIN; NICHE; MAINTENANCE; DEPEND;
D O I
10.3892/mmr.2013.1789
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Bone marrow mesenchymal stem cells (BMSCs) have been identified as an important component of the hematopoietic stem cell (HSC) niche, which is essential for the maintenance of HSCs. HSC niche alternation has been considered to be the main cause of acute myeloid leukemia (AML). However, little is known with regard to BMSC alteration in AML patients. BMSCs were collected from 10 AML patients and 13 controls in order to examine the morphology, differentiation and adhesion molecule expression changes. It was observed that primary BMSCs from AML patients exhibited aberrant morphologies compared with those from the controls. Prior to adipogenic differentiation, the mRNA and protein levels of the lipid marker gene lipoprotein lipase, from the BMSCs of AML patients, were significantly higher. lipid drops were present early during differentiation in the BMSCs of AML patients and exhibited greater numbers later. Following adipogenic differentiation, the mRNA level of E-cadherin in the BMSCs of AML patients was significantly lower than that identified in the BMSCs of the control groups. Following osteogenic induction, the mRNA level of E-cadherin in the BMSCs of AML patients was significantly higher than in the controls. Therefore BMSCs from the AML patients exhibited irregular morphology, tendency to pre-differentiate to adipocytes and different adhesion molecule expression following differentiation. These differences may further our understanding of the HSC niche in the pathological condition.
引用
收藏
页码:293 / 298
页数:6
相关论文
共 14 条
[1]
Osteoblastic cells regulate the haematopoietic stem cell niche [J].
Calvi, LM ;
Adams, GB ;
Weibrecht, KW ;
Weber, JM ;
Olson, DP ;
Knight, MC ;
Martin, RP ;
Schipani, E ;
Divieti, P ;
Bringhurst, FR ;
Milner, LA ;
Kronenberg, HM ;
Scadden, DT .
NATURE, 2003, 425 (6960) :841-846
[2]
Knockdown of N-cadherin suppresses the long-term engraftment of hematopoietic stem cells [J].
Hosokawa, Kentaro ;
Arai, Fumio ;
Yoshihara, Hiroki ;
Iwasaki, Hiroko ;
Nakamura, Yuka ;
Gomei, Yumiko ;
Suda, Toshio .
BLOOD, 2010, 116 (04) :554-563
[3]
Cadherin-Based Adhesion Is a Potential Target for Niche Manipulation to Protect Hematopoietic Stem Cells in Adult Bone Marrow [J].
Hosokawa, Kentaro ;
Arai, Fumio ;
Yoshihara, Hiroki ;
Iwasaki, Hiroko ;
Hembree, Mark ;
Yin, Tong ;
Nakamura, Yuka ;
Gomei, Yumiko ;
Takubo, Keiyo ;
Shiama, Haruko ;
Matsuoka, Sahoko ;
Li, Linheng ;
Suda, Toshio .
CELL STEM CELL, 2010, 6 (03) :194-198
[4]
Uncertainty in the niches that maintain haematopoietic stem cells [J].
Kiel, Mark J. ;
Morrison, Sean J. .
NATURE REVIEWS IMMUNOLOGY, 2008, 8 (04) :290-301
[5]
Lack of evidence that hematopoietic stem cells depend on N-cadherin-mediated adhesion to osteoblasts for their maintenance [J].
Kiel, Mark J. ;
Radice, Glenn L. ;
Morrison, Sean J. .
CELL STEM CELL, 2007, 1 (02) :204-217
[6]
Hematopoietic Stem Cells Do Not Depend on N-Cadherin to Regulate Their Maintenance [J].
Kiel, Mark J. ;
Acar, Melih ;
Radice, Glenn L. ;
Morrison, Sean J. .
CELL STEM CELL, 2009, 4 (02) :170-179
[7]
Mesenchymal and haematopoietic stem cells form a unique bone marrow niche [J].
Mendez-Ferrer, Simon ;
Michurina, Tatyana V. ;
Ferraro, Francesca ;
Mazloom, Amin R. ;
MacArthur, Ben D. ;
Lira, Sergio A. ;
Scadden, David T. ;
Ma'ayan, Avi ;
Enikolopov, Grigori N. ;
Frenette, Paul S. .
NATURE, 2010, 466 (7308) :829-U59
[8]
Bone-marrow adipocytes as negative regulators of the haematopoietic microenvironment [J].
Naveiras, Olaia ;
Nardi, Valentina ;
Wenzel, Pamela L. ;
Hauschka, Peter V. ;
Fahey, Frederic ;
Daley, George Q. .
NATURE, 2009, 460 (7252) :259-U124
[9]
Multilineage potential of adult human mesenchymal stem cells [J].
Pittenger, MF ;
Mackay, AM ;
Beck, SC ;
Jaiswal, RK ;
Douglas, R ;
Mosca, JD ;
Moorman, MA ;
Simonetti, DW ;
Craig, S ;
Marshak, DR .
SCIENCE, 1999, 284 (5411) :143-147
[10]
The molecular pathogenesis of acute myeloid leukemia [J].
Steffen, B ;
Müller-Tidow, C ;
Schwäble, J ;
Berdel, WE ;
Serve, H .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2005, 56 (02) :195-221