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
[31]   Engraftment kinetics after transplantation of double unit cord blood grafts combined with haplo-identical CD34+cells without antithymocyte globulin [J].
Politikos, Ioannis ;
Devlin, Sean M. ;
Arcila, Maria E. ;
Barone, Jonathan C. ;
Maloy, Molly A. ;
Naputo, Kristine A. ;
Ruiz, Josel D. ;
Mazis, Christopher M. ;
Scaradavou, Andromachi ;
Avecilla, Scott T. ;
Dahi, Parastoo B. ;
Giralt, Sergio A. ;
Hsu, Katherine C. ;
Jakubowski, Ann A. ;
Papadopoulos, Esperanza B. ;
Perales, Miguel A. ;
Sauter, Craig S. ;
Tamari, Roni ;
Ponce, Doris M. ;
O'Reilly, Richard J. ;
Barker, Juliet N. .
LEUKEMIA, 2021, 35 (03) :850-862
[32]   Mobilization of CD34-positive bone marrow-derived cells after coronary stent implantation - Impact on restenosis [J].
Inoue, Teruo ;
sata, Maka Sata ;
Hikichi, Yutaka ;
Sohma, Ryoichi ;
Fukuda, Daiju ;
Uchida, Toshihiko ;
Shimizu, Minoru ;
Komoda, Hiroshi ;
Node, Koichi .
CIRCULATION, 2007, 115 (05) :553-561
[33]   High D-index during mobilization predicts poor mobilization of CD34+cells after anti-lymphoma salvage chemotherapy [J].
Ebisawa, Kazutoshi ;
Honda, Akira ;
Chiba, Akira ;
Masamoto, Yosuke ;
Okazaki, Hitoshi ;
Kurokawa, Mineo .
JOURNAL OF CLINICAL APHERESIS, 2022, 37 (01) :4-12
[34]   Safety analysis and improved cardiac function following local autologous transplantation of CD133+ enriched bone marrow cells after myocardial infarction [J].
Ahmadi, Hossein ;
Baharvand, Hossein ;
Ashtiani, Saeed Kazemi ;
Soleimani, Massoud ;
Sadeghian, Hakimeh ;
Ardekani, Jalil Madjd ;
Mehrjerdi, Narges Zare ;
Kouhkan, Azam ;
Namiri, Mehrnaz ;
Madani-Civi, Manouchehr ;
Fattahi, Fatemeh ;
Shahverdi, Abdolhossein ;
Dizaji, Ahmad Vosoug .
CURRENT NEUROVASCULAR RESEARCH, 2007, 4 (03) :153-160
[35]   Influence of Cell Treatment With PDGF-BB and Reperfusion on Cardiac Persistence of Mononuclear and Mesenchymal Bone Marrow Cells After Transplantation Into Acute Myocardial Infarction in Rats [J].
Krausgrill, Benjamin ;
Vantler, Marius ;
Burst, Volker ;
Raths, Martin ;
Halbach, Marcel ;
Frank, Konrad ;
Schynkowski, Silke ;
Schenk, Kerstin ;
Hescheler, Juergen ;
Rosenkranz, Stephan ;
Mueller-Ehmsen, Jochen .
CELL TRANSPLANTATION, 2009, 18 (08) :847-853
[36]   Transplantation of CD6-depleted peripheral blood stem cells after DLA-haploidentical bone marrow transplantation contributes to engraftment and tolerance in a preclinical model of stem cell transplantation [J].
Zorn, Julia ;
Schwamberger, Sabine ;
Panzer, Werner ;
Adler, Heiko ;
Kolb, Hans-Jochem .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 2011, 144 (1-2) :27-35
[37]   IMMUNOPHENOTYPE OF BONE MARROW PLASMA CELLS IN PATIENTS WITH MULTIPLE MYELOMA DURING HIGH-DOSE CHEMOTHERAPY AND AFTER AUTOLOGOUS STEM CELL TRANSPLANTATION [J].
Mendeleeva, L. P. ;
Akhundova, F. M. ;
Naumova, E., V ;
Galtseva, I., V ;
Pokrovskaya, O. S. ;
Soloviev, M., V ;
Gribanova, E. O. ;
Kuzmina, L. A. ;
Parovichnikova, E. N. ;
Savchenko, V. G. .
GEMATOLOGIYA I TRANSFUZIOLOGIYA, 2017, 62 (01) :4-8
[38]   RETRACTED: EBF1 gene promotes the proliferation and inhibits the apoptosis of bone marrow CD34+cells in patients with myelodysplastic syndrome through negative regulation of mitogen-activated protein kinase axis (Retracted article. See vol. 122, 2021) [J].
Hou, Shuang ;
Hao, Jie ;
Wang, Yan-Yu ;
Zhao, Bing-Bing ;
Xiao, Gong-Wei ;
Li, Yan-Qing ;
Liu, Xi ;
Zou, Zhi-Lan ;
Yao, Ye ;
Xiong, Hong .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2019, 120 (02) :1407-1419
[39]   CYTOKINE ACTIVITY AFTER ALLOGENEIC BONE-MARROW TRANSPLANTATION .5. ANALYSIS OF IL-2 AND IFN PRODUCTION BY ISOLATED CD4(+) AND CD8(+) CELLS [J].
COOLEY, MA ;
WRIGHT, L ;
ATKINSON, K .
BRITISH JOURNAL OF HAEMATOLOGY, 1994, 86 (04) :702-708
[40]   DIRECT EFFECTS OF 13-CIS AND ALL-TRANS-RETINOIC ACID ON NORMAL BONE-MARROW (BM) PROGENITORS - COMPARATIVE-STUDY ON BM MONONUCLEAR-CELLS AND ON ISOLATED CD34+ BM CELLS [J].
VANBOCKSTAELE, DR ;
LENJOU, M ;
SNOECK, HW ;
LARDON, F ;
STRYCKMANS, P ;
PEETERMANS, ME .
ANNALS OF HEMATOLOGY, 1993, 66 (02) :61-66