The ultrastructure study of membrane surface of the bone marrow CD34+ cells with the atomic force microscope.
- Author:
Mei-Li LIU
1
;
Ji-Ye CAI
;
Long-Jiang YANG
;
Fan-Yi MENG
;
Xiao-Yan WANG
;
Zhi-Hong LIANG
;
Ling-Song LI
Author Information
1. Department of Chemistry, College of Life Science and Technology, Jinan University, Guangzhou, 510632, China.
- Publication Type:Journal Article
- MeSH:
Antigens, CD34;
analysis;
Bone Marrow Cells;
cytology;
immunology;
ultrastructure;
Cell Membrane;
ultrastructure;
Hematopoietic Stem Cells;
cytology;
immunology;
ultrastructure;
Humans;
Microscopy, Atomic Force
- From:
Journal of Experimental Hematology
2004;12(6):793-797
- CountryChina
- Language:Chinese
-
Abstract:
Human CD34(+) hematopoietic cells, a distinctive cell population containing hematopoietic stem/progenitor cells (HSPC), have the capability to highly self-renewal, differentiation into all lineages of committed progenitor cells and reconstitution of both long-term hematopoiesis and immunefunctions after transplantation. CD34(+) hematopoietic cells from bone marrow (BM) recently have been employed for treating neoplastic and genetic disorders. This study was aimed to investigate membrane surface ultrastructures of bone marrow CD34(+) cell from mormal persons and leukemia patients and to compare their morphologic differences by using atomic force microscope (AFM). BM was collected from 5 normal donors and 6 leukaemia patients. All samples were layered on Ficoll-Paque gradients (specific gravity 1.077 g/ml) to separate the mononuclear cells. After that CD34(+) cells were purified by immuno-magnetic bead separation and evaluated with a FACS Calibur, these cells were detected by AFM of tapping mode inair. At lest 20 cells per samples were observed. The results showed that most of CD34(+) hematopoietic cells were like circle plate, the diameter was 10 - 14 microm. The surface of CD34(+) hematopoietic cell membrane was comparatively complex. The surface of CD34(+) hematopoietic cell membrane appeared as granular, with packed particles. With the region analysis function of IP2.1 software, the region of 2 microm x 2 microm was selected and four parameters of the surface (maximum peak-to-valley distance, average roughness, root-mean-squared roughness and mean height) were measured. Values of the 4 parameters showed that the characteristic parameters of CD34(+) HSPC from leukaemia were higher than that from normal person. It is concluded that AFM has specific advantages in analyzing cell membrane in the nanometer level and can gain more information. With the help of analysis software, AFM can be a helpful tool for fast leukaemic diagnosis and CD34(+) hematopoietic cells selection.
