scholarly journals A functional comparison of CD34 + CD38- cells in cord blood and bone marrow

Blood ◽  
1995 ◽  
Vol 86 (10) ◽  
pp. 3745-3753 ◽  
Author(s):  
QL Hao ◽  
AJ Shah ◽  
FT Thiemann ◽  
EM Smogorzewska ◽  
GM Crooks

We present cell cycling and functional evidence that the CD34+CD38- immunophenotype can be used to define a rare and primitive subpopulation of progenitor cells in umbilical cord blood. CD34+CD38- cells comprise 0.05% +/- 0.08% of the mononuclear cells present in cord blood. Cell cycle analysis with the fluorescent DNA stain 7- aminoactinomycin D showed that the percentage of CD34+ cells in cycle directly correlated with increasing CD38 expression. CD34+CD38- cord blood cells were enriched for long-term culture-initiating cells (LTCIC; cells able to generate colony-forming unit-cells [CFU-C] after 35 to 60 days of coculture with bone marrow stroma) relative to CD34+CD38- cells. In an extended LTCIC assay, CD34+CD38- cells were able to generate CFU-C between days 60 and 100, clearly distinguishing them from CD34+CD38+ cells that did not generate CFU-C beyond day 40. When plated as single cells, onset of clonal proliferation was markedly delayed in a subpopulation of CD34+CD38- cells; clones (defined as = 100 cells) appeared after 60 days of culture in 2.9% of CD34+CD38- cells. In contrast, 100% of CD34+CD38+ cells formed clones by day 21. Although the CD34+CD38- immunophenotype defines highly primitive populations in both bone marrow and cord blood, important functional differences exist between the two sources. CD34+CD38- cord blood cells have a higher cloning efficiency, proliferate more rapidly in response to cytokine stimulation, and generate approximately sevenfold more progeny than do their counterparts in bone marrow.

2019 ◽  
Vol 28 (9-10) ◽  
pp. 1329-1332 ◽  
Author(s):  
Paul R. Sanberg ◽  
Jared Ehrhart

The therapeutic application of human umbilical cord blood cells has been an area of great interest for at least the last 25 years. Currently, cord blood cells are approved for reconstitution of the bone marrow following myeloablation in both young and old patients with myeloid malignancies and other blood cancers. Translational studies investigating alternative uses of cord blood have also shown that these cells not only stimulate neurogenesis in the aged brain but are also potentially therapeutic in the treatment of adult neurodegenerative disorders including amyotrophic lateral sclerosis, Alzheimer’s disease, ischemic stroke, traumatic brain injury, and Parkinson’s disease. Recent advances in the clinical application of cord blood cells by Dr. Joanne Kurtzberg and colleagues have found that non-HLA matched allogeneic banked cord blood units in immunocompetent patients with ischemic stroke are safe and well tolerated. Although the exact mechanism(s) of action that provide the beneficial effects observed from a cord blood cell-based therapy are currently unknown, several studies using models of neurodegenerative disease have shown these cells are immune-modulatory and anti-inflammatory. Thus, any future clinical studies investigating the efficacy of this cord blood cell therapeutic would strongly benefit from the inclusion of methodologies to determine changes in both markers of inflammation and the response of immune tissues, such as the spleen, in subjects receiving cell infusion.


2020 ◽  
Vol 14 ◽  
pp. 117793222091330
Author(s):  
LM Avila-Portillo ◽  
F Aristizabal ◽  
S Perdomo ◽  
A Riveros ◽  
B Ospino ◽  
...  

Biosimilars of granulocyte colony-stimulating factor (G-CSF) have been routinely introduced into clinical practice. However, not functional genomics characterization has been performed yet in comparison with the innovator G-CSF. This study aimed to evaluate the transcriptomic changes in an in vitro model of umbilical cord blood cells (UBC) exposed to G-CSF for the identification of their modulated pathways. Umbilical cord blood cells–derived mononuclear cells (MNCs) were treated with biosimilar and innovator G-CSF for further gene expression profiling analysis using a microarray-based platform. Comparative analysis of biosimilar and innovator G-CSF gene expression signatures allowed us to identify the most commonly modulated pathways by both drugs. In brief, we observed predominantly upmodulation of transcripts related to PI3K-Akt, NF-kappaB, and tumor necrosis factor (TNF) signaling pathways as well as transcripts related to negative regulation of apoptotic process among others. In addition, hematopoietic colony-forming cell assays corroborate the G-CSF phenotypic effects over UBC-derived MNCs. In conclusion, our study suggests that G-CSF impacts UBC-derived cells through the modulation of several signaling pathways associated with cell survival, migration, and proliferation. The concordance observed between biosimilar and innovator G-CSF emphasizes their similarity in regards to their specificity and biological responses.


Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 3190-3190 ◽  
Author(s):  
Adalberto Ibatici ◽  
Anna Maria Raiola ◽  
Marina Podesta ◽  
Sarah Pozzi ◽  
Silvia Lucchetti ◽  
...  

Abstract The major limit of cord blood (CB) transplant in adult patients is represented by the delayed engraftment. Newer approaches have been suggested including double cord blood transplant and infusion of CD34+ selected cells from a relative to achieve a transient engraftment until CB cells generate mature blood cells. Our initial pre-clinical studies showed that intra-bone injection of hematopoietic cells in the mouse was associated with an engraftment about 10 times more efficient with respect to the usual intravenous injection. Moreover, we had already demonstrated that the defect of cord blood cells in term of delayed engraftment was not related to the lower number of hematopoietic cells infused since the capacity to reconstitute the host stem cell reservoir was higher than adult bone marrow. Therefore, we set-up a pilot study to evaluate whether this type of transplant could shorten the time of engraftment. Five patients [4 male (M) and 1 female (F)] have been enrolled in this study. Clinical characteristics at transplant were: three patients had acute myeloid leukaemia: 2 refractory-relapsing and one in 1st CR (age 37 M, 50 M, 60 M) and 2 acute lymphoblastic leukaemia: one in 1st CR and one in 2nd CR (age 42 F, 18 M). Cord Blood grafts were matched as follows: 3/6 in one patients, 4/6 in three patients, and 5/6 in one patient for HLA-A, B, DRB1 (serology for HLA class I and allelic for class II). Patients were prepared with standard conditioning including TBI. Anti-Thymocyte-Globulin 3.75mg/kg was given on day −3,−2. GVHD Prophylaxis was cyclosporine from day -7 (therapeutic range 200–400 ng /ml) plus mycophenolate-mofetil 15mg/kg b.i.d. from day +1 to +28. The number of cord blood cells infused was 2.4, 1.6, 2.4, 3.0, 2.7 x 10^7/kg b.w. Cells were infused under very short general anaesthesia (propofol) of 5–10 minutes in the posterior iliac crest with a standard bone marrow aspiration needle (gauge n. 14). Before infusion, CB cells were washed to eliminate DMSO. Sustained engraftment of PMN (more than 3 consecutive days > 500 PMN x10^9/l) was recorded at day: + 20, 25, 18, 20, 23. Platelets sustained engraftment (more than 3 consecutive days > 20.000 Platelets x10^9/l) was recorded at day: +32, 42, 25, 29, 31.Acute GVHD was absent in these five patients. This is a pilot study with very short follow-up (2 to 5 months). Thus, no conclusive answer can be drawn on the impact of this technique on the final outcome of these patients. However, the time to PMN and Platelets engraftment is much shorter with respect to the available data obtained with intra-venous (IV) injection of the same amount of cells. Seeding efficiency experiments have shown that less than 10% of the injected cells via IV actually seed in the active hematopoietic sites. Cord blood cells, injected directly into the bone marrow, may undergo a better homing without loss, proliferate and finally colonise the rest of the bone marrow; thus, improving considerably the seeding efficiency. Alternatively, CB cells may undergo faster maturation if injected intra-bone marrow and, at the same time, colonise more efficiently the rest of active hematopoietic sites. If confirmed in larger studies, this approach may render cord blood cells transplant suitable for a greater number of adult patients who so far were excluded from this therapeutic option. This work was supported by AIRC, CARIGE; Compagnia di San Paolo.


Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 3650-3650
Author(s):  
Kent W. Christopherson ◽  
Tiki Bakhshi ◽  
Shamanique Bodie ◽  
Shannon Kidd ◽  
Ryan Zabriskie ◽  
...  

Abstract Hematopoietic Stem Cells (HSC) are routinely obtained from bone marrow, mobilized peripheral blood, and umbilical Cord Blood. Traditionally, adult bone marrow has been utilized as a source of Mesenchymal Stem Cells (MSC). Bone marrow derived MSC (BM-MSC) have previously been shown to maintain the growth of HSC obtained from cord blood and have been utilized for cord blood expansion purposes. However, the use of a mismatched BM-MSC feeder stromal layer to support the long term culture of cord blood HSC is not ideal for transplant purposes. The isolation of MSC from a novel source, the Wharton’s Jelly of Umbilical Cord segments, was recently reported (Romanov Y, et al. Stem Cells.2003; 21: 105–110) (Lee O, et al. Blood.2004; 103: 1669–1675). We therefore hypothesized that Umbilical Cord derived MSC (UC-MSC) have the ability to support the long term growth of cord blood derived HSC similar to that previously reported for BM-MSC. To test this hypothesis, MSC were isolated from the Wharton’s Jelly of Umbilical Cord segments and defined morphologically and by cell surface markers. UC-MSC were then tested for their ability to support the growth of pooled CD34+ cord blood cells in long term culture - initiating cell (LTC-IC) assays as compared to BM-MSC. We observed that like BM-MSC, CB-MSC express a defined set of cell surface markers. By flow cytometry we determined that that both UC-MSC and BM-MSC are positive for CD29, CD44, CD73, CD90, CD105, CD166, HLA-A and negative for CD45, CD34, CD38, CD117, HLA-DR expression. Utilizing Mitomycin C treated (200 μM, 15 min.) UC-MSC from multiple donors as a feeder layer we observed that UC-MSC have the ability to support the maintenance of long term hematopoiesis during the LTC-IC assay. Specifically, UC-MSC isolated from separate umbilical cord donors support the growth of 69.6±11.9 (1A), 31.7±3.9 (2B), 67.0±13.5 (3A), and 38.5±13.7 (3B) colony forming cells (CFC) per 1×104 CD34+ cord blood cells as compared to 64.0±4.2 CFC per 1×104 CD34+ cord blood cells supported by BM-MSC (Mean±SEM, N=4 separate segments from three different donors). Thus, Umbilical Cord derived Mesenchymal Stem Cells, a recently described novel source of MSC, have the ability to support long term maintenance of Hematopoietic Stem Cells, as defined by the LTC-IC assay. These results may have potential therapeutic application with respect to ex vivo stem cell expansion of Cord Blood Hematopoietic Stem Cells utilizing a Mesenchymal Stem Cell stromal layer. In addition, these data suggest the possibility of co-transplantation of matched Mesenchymal and Hematopoietic Stem Cells from the same umbilical cord and cord blood donor respectively. Lastly, these results describe a novel model system for the future study of the interaction between Cord Blood Hematopoietic Stem Cells and the appropriate supportive microenvironment represented by the Umbilical Cord - Mesenchymal Stem Cells.


Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 4206-4206
Author(s):  
Angela C. Luzo ◽  
Adriana S. Duarte ◽  
Anderson F. Cunha ◽  
Dulcineia M. Albuquerque ◽  
Barbara C. Monte-Mor ◽  
...  

Abstract Hematopoietic stem/progenitor cells with their dual ability for self-renewal, expansion and multilineage differentiation constitute an essential component of hematopoietic transplantation. These qualities, together with their transfection capacity make them useful for gene therapy also. Umbilical cord blood and bone marrow represent efficient sources of these cells. Cord blood stem cells are more primitive than bone marrow cells. They have a greater capacity to self-renewal, proliferation, expansion, multilineage differentiation and are better transfected. They can also be transplanted without complete HLA compatibility. Some recent studies are demonstrating that they could have a better trafficking and homing than the others, which could promote an efficient development and proliferation in the marrow microenvironment and better recovering when transplanted. However, these mechanisms of migration/cell adhesion and cell cycle are not fully understood. The aim of this study is to compare cord blood mononuclear cells with the existing bone marrow mononuclear cells library (esage database) by means of serial analysis of gene expression in order to investigate if there are any differences that could explain those findings. We obtained, by sequencing the SAGE library of cord blood cells, a total of 44.924 tags representing 15.519 unique tags. These unique tags were distribute as: known genes= 7772; sequence predicted or annotated=3935; no matches= 3812. The bone marrow library showed total tags=36577 being unique tags=13075: known genes= 6711; sequence predicted or annotated = 3371; no matches= 2993. These genes were annotated using Gene Ontology Consortium and the distribution of the categories in both libraries was similar. The different expression genes, selected using the fold difference (fold≥5 and ≤ 5), were 238. In order to validate the library, we tested 12 different expressed genes by real time PCR. The first six of them (SMARCC2, CDC25B, S100-8, alpha-globin, beta-globin, gamma-globin) confirmed the SAGE results. The more expressed cord blood genes were SMARCC2, CDC25B and gamma-globin. Beta-globin, and S100-8 were more expressed in bone marrow. The alpha- globin result demonstrated almost the same result between cord blood and bone marrow. CDC25B is a member of the CDC25, family of phosphatases, it activates cyclin dependent kinase CDC2 which is required for entry into mitoses. SMARCC2 is a member of SWI/SNF family proteins which display helicase and ATPase activities. It is responsible for regulation of transcription of certain genes by altering the chromatin structure around those genes. S100-8 is a calcium binding protein with a prominent role in leukocyte trafficking. It stimulates shedding of L-selectin, which is also involved in cell adhesion. It makes a role in inflammatory process towards neutrophil migration to inflammatory sites. The alpha, beta and gamma globin results were those expected based on the ontogeny. The differential gene expression here obtained could be an important tool to guide new functional studies regarding the molecular mechanisms of homing, cell cycle and cell adhesion of cord blood cells.


2004 ◽  
Vol 32 (8) ◽  
pp. 782-787 ◽  
Author(s):  
Sandra Castello ◽  
Marina Podestà ◽  
Vincenzo G. Menditto ◽  
Adalberto Ibatici ◽  
Anna Pitto ◽  
...  

2007 ◽  
Vol 31 (5) ◽  
pp. 643-651 ◽  
Author(s):  
Edward B. Garon ◽  
Laura Marcu ◽  
Quang Luong ◽  
Oxana Tcherniantchouk ◽  
Gay M. Crooks ◽  
...  

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