Survival of cord blood haematopoietic stem cells in a hyaluronan hydrogel for ex vivo biomimicry

被引:16
|
作者
Demange, Elise [1 ]
Kassim, Yusra [1 ]
Petit, Cyrille [1 ]
Buquet, Catherine [1 ]
Dulong, Virginie [2 ]
Le Cerf, Didier [2 ]
Buchonnet, Gerard [3 ]
Vannier, Jean-Pierre [1 ]
机构
[1] Univ Rouen, Lab MERCI EA3829, F-76183 Rouen, France
[2] Univ Rouen, Lab Polymers, Mont St Aignan, France
[3] Univ Rouen Hosp, Rouen, France
关键词
hyaluronan; migration; hydrogel; haematopoietic stem cells; scaffold; RGD; IN-VITRO; PROGENITOR CELLS; BONE-MARROW; 3-DIMENSIONAL CULTURE; CD34(+) CELLS; SELF-RENEWAL; EXPANSION; SYSTEM; MODEL; DIVISIONS;
D O I
10.1002/term.1482
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Haematopoietic stem cells (HSCs) and haematopoietic progenitor cells (HPCs) grow in a specified niche in close association with the microenvironment, the so-called haematopoietic niche'. Scaffolds have been introduced to overcome the liquid culture limitations, mimicking the presence of the extracellular matrix (ECM). In the present study the hyaluronic acid scaffold, already developed in the laboratory, has been used for the first time to maintain long-term cultures of CD34(+) haematopoietic cells obtained from human cord blood. One parameter investigated was the impact on ex vivo survival of CD34(+) cord blood cells (CBCs) on the hyaluronic acid surface, immobilized with peptides containing the RGD motif. This peptide was conjugated by coating the hyaluronan hydrogel and cultured in serum-free liquid phase complemented with stem cell factor (SCF), a commonly indispensable cytokine for haematopoiesis. Our work demonstrated that these hyaluronan hydrogels were superior to traditional liquid cultures by maintaining and expanding the HPCs without the need for additional cytokines, and a colonization of 280-fold increment in the hydrogel compared with liquid culture after 28days of ex vivo expansion. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:901 / 910
页数:10
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