Protection of bone marrow, mononuclear, and CD34+cells by enclosing within the biochemical compound solution during and after transplantation

被引:0
作者
Qujeq, Durdi [1 ,2 ]
Abedian, Zeinab [1 ]
机构
[1] Babol Univ Med Sci, CMBRC, Hlth Res Inst, Babol Sar, Iran
[2] Babol Univ Med Sci, Dept Clin Biochem, Fac Med, Babol Sar, Iran
关键词
bone marrow; CD34+cells; functionality; mononuclear; viability; CELL TRANSPLANTATION; STEM-CELLS; HYDROGELS; DIFFERENTIATION; PROPOLIS; THERAPY;
D O I
10.1002/cbf.3275
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have chosen collagen, chitosan acetate, hyaluronic acid, and propolis as model biochemical compound solution to determine the influence of cell carrier mechanics on cell viability and functionality during and after transplantation. Suspending of bone marrow (BM), mononuclear (MN), and CD34+ cells into a biochemical compounds solution is an attractive tool to achieve to protect and ensure reproducible deliver. Hyperglycemic rats were randomly divided into 2 groups: to receive no cell treatment or approximately 1x10(5) of BM, MN, and CD34+ cells within the PBS or biochemical compound solution. These cells were infused into the hyperglycemic rats on day 10 and again on day 20. At each time point, the animals were anaesthetized with ether, and 200L of blood was drawn from the tail vein. Samples were collected to determine whether BM, MN, and CD34+ cell affected glucose content and insulin production. Our results exhibit the use of biochemical compound solution method to overcome the cell transplantation problem during and after injection of these cells into rats. These findings are supported by resulting in significantly greater insulin production and more decreased glucose content than cells injected in PBS only (P<0.05). These effects displayed the following hierarchy: hyaluronic acid>chitosan acetate>collagen>propolis solution. Our results showed that these compounds demonstrated a capacity to encapsulate the BM, MN, and CD34+ cells. It is proven by decreasing glucose content and increasing insulin secretion by pancreatic cells. The uniqueness of our study is the improvement of current transplantation efficiency.
引用
收藏
页码:352 / 357
页数:6
相关论文
共 50 条
[41]   A low CD34+ cell dose results in higher mortality and poorer survival after blood or marrow stem cell transplantation from HLA-identical siblings: should 2 × 106 CD34+ cells/kg be considered the minimum threshold? [J].
S Singhal ;
R Powles ;
J Treleaven ;
S Kulkarni ;
B Sirohi ;
C Horton ;
B Millar ;
V Shepherd ;
D Tait ;
R Saso ;
A Rowland ;
S Long ;
J Mehta .
Bone Marrow Transplantation, 2000, 26 :489-496
[42]   Patients suffering from acute graft-versus-host disease after bone-marrow transplantation have functional CD4+CD25hiFoxp3+ regulatory T cells [J].
Noel, G. ;
Bruniquel, D. ;
Birebent, B. ;
DeGuibert, S. ;
Grosset, J-M. ;
Bernard, M. ;
Dauriac, C. ;
Chevallier, P. ;
Lamy-de-la-chapelle, T. ;
Semana, G. ;
Brinster, C. .
CLINICAL IMMUNOLOGY, 2008, 129 (02) :241-248
[43]   Long-term myocardial functional improvement after autologous bone marrow mononuclear cells transplantation in patients with ST-segment elevation myocardial infarction: 4 years follow-up‡ [J].
Cao, Feng ;
Sun, Dongdong ;
Li, Chengxiang ;
Narsinh, Kazim ;
Zhao, Li ;
Li, Xue ;
Feng, Xuyang ;
Zhang, Jun ;
Duan, Yunyan ;
Wang, Jing ;
Liu, Dingjing ;
Wang, Haichang .
EUROPEAN HEART JOURNAL, 2009, 30 (16) :1986-1994
[44]   A low CD34+ cell dose results in higher mortality and poorer survival after blood or marrow stem cell transplantation from HLA-identical siblings:: should 2 x 106 CD34+ cells/kg be considered the minimum threshold? [J].
Singhal, S ;
Powles, R ;
Treleaven, J ;
Kulkarni, S ;
Sirohi, B ;
Horton, C ;
Millar, B ;
Shepherd, V ;
Tait, D ;
Saso, R ;
Rowland, A ;
Long, S ;
Mehta, J .
BONE MARROW TRANSPLANTATION, 2000, 26 (05) :489-496
[45]   Functional expression of high-affinity receptor for immunoglobulin E on mast cells precedes that of tryptase during differentiation from human bone marrow-derived CD34 progenitors cultured in the presence of stem cell factor and interleukin-6 [J].
Shimizu, Y ;
Suga, T ;
Maeno, T ;
Aoki, F ;
Tsukagoshi, H ;
Kawata, T ;
Sakai, K ;
Narita, T ;
Takahashi, T ;
Ishikawa, S ;
Morishita, Y ;
Nakajima, T ;
Hara, F ;
Miura, T ;
Kurabayashi, M .
CLINICAL AND EXPERIMENTAL ALLERGY, 2004, 34 (06) :917-925
[46]   Characterization of 'adult-type' mast cells derived from human bone marrow CD34+ cells cultured in the presence of stem cell factor and interleukin-6.: Interleukin-4 is not required for constitutive expression of CD54, FcεRIα and chymase, and CD13 expression is reduced during differentiation [J].
Shimizu, Y ;
Sakai, K ;
Miura, T ;
Narita, T ;
Tsukagoshi, H ;
Satoh, Y ;
Ishikawa, S ;
Morishita, Y ;
Takai, S ;
Miyazaki, M ;
Mori, M ;
Saito, H ;
Xia, H ;
Schwartz, LB .
CLINICAL AND EXPERIMENTAL ALLERGY, 2002, 32 (06) :872-880
[47]   Intracoronary infusion of bone marrow-derived selected CD34+CXCR4+ cells and non-selected mononuclear cells in patients with acute STEMI and reduced left ventricular ejection fraction: results of randomized, multicentre Myocardial Regeneration by Intracoronary Infusion of Selected Population of Stem Cells in Acute Myocardial Infarction (REGENT) Trial [J].
Tendera, Michal ;
Wojakowski, Wojciech ;
Ruzyllo, Witold ;
Chojnowska, Lidia ;
Kepka, Cezary ;
Tracz, Wieslawa ;
Musialek, Piotr ;
Piwowarska, Wieslawa ;
Nessler, Jadwiga ;
Buszman, Pawel ;
Grajek, Stefan ;
Breborowicz, Piotr ;
Majka, Marcin ;
Ratajczak, Mariusz Z. .
EUROPEAN HEART JOURNAL, 2009, 30 (11) :1313-1321
[48]   Bone Marrow CD34+/lin- Cells of Patients with Chronic-Phase Chronic Myeloid Leukemia (CP-CML) After 12 Months of Nilotinib Treatment Exhibit a Different Gene Expression Signature Compared to the Diagnosis and the Corresponding Cells from Healthy Subjects [J].
Trojani, Alessandra ;
Pungolino, Ester ;
Di Camillo, Barbara ;
Bossi, Luca Emanuele ;
Palumbo, Cassandra ;
D'adda, Mariella ;
Perego, Alessandra ;
Turrini, Mauro ;
Elena, Chiara ;
Borin, Lorenza Maria ;
Iurlo, Alessandra ;
Malato, Simona ;
Spina, Francesco ;
Latargia, Maria Luisa ;
Spedini, Pierangelo ;
Artale, Salvatore ;
Anghilieri, Michela ;
Carraro, Maria Cristina ;
Bucelli, Cristina ;
Beghini, Alessandro ;
Cairoli, Roberto .
CANCERS, 2025, 17 (06)
[49]   CD34+cell dose effects on clinical outcomes after T-cell replete haploidentical allogeneic hematopoietic stem cell transplantation for acute myeloid leukemia using peripheral blood stem cells. A study from the acute leukemia working Party of the European Society for blood and marrow transplantation (EBMT) [J].
Maffini, Enrico ;
Labopin, Myriam ;
Blaise, Didier ;
Ciceri, Fabio ;
Gulbas, Zafer ;
Deconinck, Eric ;
Leblond, Veronique ;
Chevallier, Patrick ;
Socie, Gerard ;
Araujo, Mercedes C. ;
Koc, Yener ;
Savani, Bipin N. ;
Gorin, Norbert C. ;
Lanza, Francesco ;
Nagler, Arnon ;
Mohty, Mohamad .
AMERICAN JOURNAL OF HEMATOLOGY, 2020, 95 (08) :892-899
[50]   Recipient Myeloid-Derived Immunomodulatory Cells Induce PD-1 Ligand-Dependent Donor CD4+Foxp3+ Regulatory T Cell Proliferation and Donor-Recipient Immune Tolerance after Murine Nonmyeloablative Bone Marrow Transplantation [J].
van der Merwe, Marie ;
Abdelsamed, Hossam A. ;
Seth, Aman ;
Ong, Taren ;
Vogel, Peter ;
Pillai, Asha B. .
JOURNAL OF IMMUNOLOGY, 2013, 191 (11) :5764-5776