Juopperi Tarja A, Schuler William, Yuan Xuan, Collector Michael I, Dang Chi V, Sharkis Saul J
Graduate Program of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.
Exp Hematol. 2007 Feb;35(2):335-41. doi: 10.1016/j.exphem.2006.09.014.
Our laboratory has established two unique methods to isolate murine hematopoietic stem cells on the basis of functional characteristics such as the ability of stem cells to home to bone marrow and aldehyde dehydrogenase (ALDH) activity. An essential component of both protocols is the separation of whole bone marrow into small-sized cells by counter-flow elutriation. We sought to provide the scientific community with an alternate approach to acquire our stem cells by replacing elutriation with the use of density-gradient centrifugation.
The elutriated fraction 25 population was characterized based on density using a discontinuous gradient. The long-term reconstituting potential of whole bone marrow cells collected at each density interface was determined by subjecting the fractions to the two-day homing protocol, transplanting them into lethally irradiated recipient mice, and assessing peripheral blood chimerism. We also investigated the ability of high-density bone marrow cells isolated in conjunction with the ALDH protocol to repopulate the hematopoietic system of myeloablated recipients.
Bone marrow cells collected at the high-density interface of 1.081/1.087 g/mL (fraction 3) had the capacity for homing to marrow and the ability to provide long-term hematopoietic reconstitution. Fraction three lineage-depleted ALDH-bright cells could also engraft and provide long-term hematopoiesis at limiting dilutions.
Density-gradient centrifugation can be used in conjunction with either of our stem cell isolation protocols to obtain cells with long-term reconstitution ability. We anticipate that this strategy will encourage and enable investigators to study the biology of HSCs isolated using functional characteristics.
我们的实验室基于干细胞归巢至骨髓的能力和醛脱氢酶(ALDH)活性等功能特性,建立了两种独特的分离小鼠造血干细胞的方法。这两种方案的一个重要组成部分是通过逆流淘析将全骨髓分离成小细胞。我们试图为科学界提供一种替代方法,通过使用密度梯度离心取代淘析来获取我们的干细胞。
使用不连续梯度基于密度对淘析的第25部分群体进行表征。通过对每个密度界面收集的全骨髓细胞进行为期两天的归巢方案,将它们移植到接受致死性照射的受体小鼠中,并评估外周血嵌合率,来确定每个密度界面收集的全骨髓细胞的长期重建潜力。我们还研究了与ALDH方案联合分离的高密度骨髓细胞重建清髓受体造血系统的能力。
在1.081/1.087 g/mL的高密度界面(第3部分)收集的骨髓细胞具有归巢至骨髓的能力和提供长期造血重建的能力。第3部分去除谱系的ALDH高表达细胞在有限稀释度下也能植入并提供长期造血。
密度梯度离心可与我们的任何一种干细胞分离方案联合使用,以获得具有长期重建能力的细胞。我们预计,这一策略将鼓励并使研究人员能够研究利用功能特性分离的造血干细胞的生物学特性。