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Kordon Kanı Hücrelerinin Saklanmasında Vitrifikasyon Metodu

Vitrification method in banking of cord blood mononuclear cells

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Abstract (2. Language): 
Objectives: The idea of protection of stem cells in a cord blood bank for treatment of various diseases, becomes more widespread. The methods when used during the protection, must be developed for minimizing the risk of cell lost. According to our purpose, we made a comparison by using different protection methods for the cord blood stem cells, during the experiments. Methods: “Density-gradient” method was used for mononuclear cell separation from cord blood, which is taken from voluntary donors. We applied 2 different vitrification method. One of them consist of two steps. Before and after the freezing process, cell viabilities by trypan blue dye method, differences in CD34+, CD45+ and CD34+45+ cells ratio by flow cytometry method and, differences in morphology by light microscope had been determinated. Results: According to our experiment results, CD45+, CD34+ and CD34+/45+ cell ratios significantly decreased after vitrification processes. But there is no significant differences between 2 different vitrification method, we used. In the light microscopy analysis, cell membran structures have damaged, cells have seen like swell and cells come together and have seen attaching. Conclusion: Vitrification methods are usefull for cell banking because of their short, cheap and easy process. We are thinking that our study is helpful for improving new and suitable methods.
Abstract (Original Language): 
Amaç: Çeşitli hastalıkların tedavisinde uygulayabilmek amacı ile kök hücrelerin saklanarak sürekli bir kök hücre bankasında toplanması fikri giderek yaygın hale gelmektedir. Saklanma sırasında hücre kaybının en aza indirilmesi için kullanılan metotların geliştirilmesi gerekmektedir. Çalışmamızda, kordon kanlarından ayrılan mononükleer hücrelere farklı saklama yöntemleri uygulayarak, yapılan karşılaştırmalar sonucunda hangi yöntemin daha verimli olduğunu belirlemek amaçlanmıştır. Yöntem: Gönüllü vericilerden alınan kordon kanlarından mononükleer hücreler, yoğunluk derecelendirme yöntemi kullanılarak ayrıldı. Biri tek aşamalı diğeri iki aşamalı olarak 2 ayrı vitrifikasyon metodu uygulandı. Vitrifikasyon öncesi ve sonrasında tripan mavisi boyama yöntemi ile hücre canlılığındaki, akım sitometri tekniği kullanılarak CD34+, CD45+ ve CD34+45+ hücre oranlarındaki, ışık mikroskobu kullanarak morfolojide meydana gelen farklılıklar belirlendi. Bulgular: Elde ettiğimiz bulgular sonucunda, dondurma öncesi ve sonrasında CD45+, CD34+, CD34+/45+ hücre oranlarında anlamlı düşüşler gözlendi. İstatistiksel değerlendirmelerde, uygulanan iki farklı vitrifikasyon metodu arasında anlamlı bir fark görülmedi. Yapılan ışık mikroskobi değerlendirmelerinde ise hücrelerin dondurma sonrasında membran yapılarının bozulduğu, hücrelerde şişmeler oluştuğu ve hücre kümeleri meydana geldiği görüldü. Sonuç: Çalışmamızda vitrifikasyon sonrası hücre kayıpları saptansa da kordon kanı hücrelerinin saklanmasında zamandan ve maddi açıdan tasarruf sağlayacak vitrifikasyon tekniklerinin kullanılabilirliğinin sağlanmasının, kordon kanı bankaları ve diğer kök hücre depolama merkezleri açısından da kullanışlı olacağı açıktır.
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REFERENCES

References: 

Kaynaklar
1. Okumuş N. Kordon kanı mononükleer hücrelerinin
fenotipik karakterizasyonu ve NK aktivitesi. istanbul
Üniversitesi Sağlık Bilimleri Enst. immünoloji Yüksek
Lisans Tezi. istanbul, 2003.
2. Broxymeyer HE, Smith FO. Cord blood stem cell transplantation.
In: Thomas D, Blume KG, Forman SJ, eds.
Hematopoietic cell transplantation. 2nd ed. London:
Blackwell; 1999. pp. 431-443.
3. Nash RA. Hematopoietic stem cell transplantation. In:
Lee GR, Forester J, Lukens J, Parakevas F, Greer JP,
Rodgers GM, eds. Wintrobe’s Clinical Hematology.
10th ed. Baltimore: Williams and Wilkins; 1999. pp.
875-896
4. Ramsey NKC. Bone marrow transplantation pediatric
oncology. Pizzo PA, Poplack DG, eds. In Principle
and Practice of Pediatric Oncology. 2nd ed.
Philadelphia; Lippincott; 1993. pp. 314-344.
5. Armitage JO. Bone marrow transplantation. N Engl J
Med 1994; 330: 827-838.
6. Han P, Hodge G, Story C, Xu X. Phenotypic analysis of
functional T-lymphocyte subtypes and natural killer
cells in human cord blood: releveance to umbilical
cord blood transplantation. Br J Haematol 1995; 89:
733-740.
7. Almici C. Biologic and phenotypic analysis of early
hematopoietic progenitor cells in umbilical cord
blood. Leukemia 1997; 11: 2143-2149.
8. Broxmeyer HE, Douglas GW, Hangoc G, et al. Human
umbilical cord blood as a potential source of transplantable
hematopoietic stem/progenitor cells. Proc
Natl Acad Sci USA 1989; 86: 3828-3832.
9. Wagner JE, De Fort T, Rubinstein P, et al.
Transplantation of unreleated donor umbilical cord
blood: outcomes and analysis of risk factors. Blood
1997; 90: 398-402.
10. Laughlin MJ, Baeker JI, Bambach B, et al.
Hematopoietic engrafment and survival in adult recipients
of umbilical-cord blood from unrelated donors.
N Engl J Med 2001; 344: 1815-1822.
11. Barker JN, Wagner JE. Umbilical cord blood transplantation:
current state of the art. Curr Opin Oncol
2002; 14:160-164.
12. Gluckman E, Rocha V, Boyer Chammard A, et al.
Eurocord Transplant Group and the European Blood
and Marrow Transplantation Group. Outcome of cordblood
transplantation from related and unrelated
donors. N Engl J Med 1997; 337: 373-381.
13. Mc Guckin CP, Forraz N, Baradoz MO, et al.
Production of stem cells with embryonic characteristics
from human umblical cord blood. Cell
Proliferation 2005; 38: 245.
14. Dooley DC, Oppenlander BK, Xiano M. Analysis of
primitive CD34- and CD34+ hematopoietic cells from
adults: gain and loss of CD34 antigen by undifferantiated
cells are closely linked to proliferative status in
culture. Stem Cells 2004; 22: 556-569.
Cerrahpafla T›p Derg 2009; 40(2): 53-62
15. Goodel M. CD34- or CD34+: does it really matter?
Blood 1999; 94: 2545-2547.
16. Chang H, Jensen L, Quesenberry P, et al.
Standardizations of hematopoietic stem cell assays: a
summary of workshops and working group meeting
sponsored by National Heart Lung and Blood Institute
and held at National Institutes of Health, Bethesta,
MD, on September 8-9, 1998 and July 30, 1999. Exp
Hematol 2000; 28: 743-752.
17. Civin CI, Almeida-Porada G, Lee MJ, et al. Sustained,
retransplantable multilineage engraftment of highly
purified bone marrow adult stem cells in vivo. Blood
1996; 88: 4102-4109.
18. Michallet M, Thiebaut A, Philip I, et al.
Transplantation with selected autologous peripheral
blood CD34+ Thy1+ hematopoietic stem cells (HSC)
in multiple myeloma: impact of HSC dose on engrafment,
safety and immun reconstitution. Exp Hematol
2000; 28: 858-870.
19. Kreissig K, Krisch A, Serke S. Characterization and
measurement of CD34- expressing haemopoietic cells.
J of Haemattherapy 1994; 3: 263-289.
20. Janowska-Wieczorek A, Majka M, Ratajczak J,
Ratajczak MZ. Autocrine/paracrine mechanisms in
human hematopoiesis. Stem Cells 2001; 19: 99-107.
21. Sogo S, Inaba M, Ogata H, et al. Inducti›n of c-kit molecules
on human CD34+/c-kit low cells: evidence for
CD34+/c-kit low cells as primitive hematopoietic stem
cells. Stem Cells 1997; 93: 2302-2307.
22. Süzergöz F. Büyüme faktörleriyle uyarılmış kordon
kanı mononükleer hücrelerinin in vitro kültürlerde
proliferasyonu ve immünfenotipik özelliklerinin incelenmesi.
istanbul Üniversitesi Sağlık Bilimleri Ens.,
İmmünoloji Doktora Tezi. İstanbul, 2002.
23. Simmons PJ, Torok Storb B. CD34 expression by stromal
precursors in normal human adult bone marrow.
Blood 1991; 78: 2848-2853.
24. Civin CI, Banquerigo ML, Strauss LC, et al. Antigenic
analysis of hematopoiesis flow cytometric characterization
of My 10 positive progenitor cells in normal
human bone marrow. Exp Hematol 1987; 15: 10-17.
25. Pasino M, Lanza T, Marotta F, et al. Flow cytometric
and functional characterization of AC133 cells from
human umbilical cord blood. BJ Haematol 2000; 108:
793-800.
26. Dhot Col PS, Sirohi Maj D, Swamy Brig GLN.
Collection, separation, enumeration and cryopreservation
of umbilical cord blood haematopoietic stem cellsan
experimental study. MJAFI 2003; 59: 298-301.
27. Meyer TPH, Hofmann B, Zaisserer J, et al. Analysis
and cryopreservation of hematopoietic stem and progenitor
cells from umbilical cord blood. Cytotherapy
2006; 8: 265-276.
28. Shreffler WG, Visness CM, Burger M, et al.
Standardization and performance evaluation of
mononuclear cell cytokine secretion assays in a multicenter
study. BMC Immunology 2006; 7: 29.
29. Chivu M, Diaconu CC, Bleotu C, Alexiu I, Brasoveanu
L, Cerescu C. The comparison of different protocols for
expansion of umbilical cord blood hematopoetic stem
cells. J Cell Mol Med 2004; 8: 223-231.
30. Todaro AM, Pafumi C, Pernicone G, et al.
Haematopoietic progenitors from umbilical cord
blood. Blood Purif 2000; 18: 144-147.
31. Kekarainen T, Mannelin S, Laine J, Jaatinen T.
Optimization of immunmagnetic separation for cord
blood-derived HSCs. BMC Cell Biology 2006; 7: 30.
32. Cairo MS, Wagner JE. Placental and/or umbilical cord
blood: an alternative source of hematopoietic stem
cells for transplantation. Blood 1997; 90: 4665-4978.
33. Moezzi L, Pourfathollah AA, Alimoghaddam K,
Soleimani M, Ardjmand AR. The effect of cryopreservation
on clonogenic capacity and in vitro expansion
potential of umbilical cord blood progenitor cells.
Transplan Proc 2005; 37: 4500-4503.
34. Ryu KH, Shin HY, Ahn HS, Kim YJ, Woo SY, Seoh JY.
Comparison of efficiency of ex vixo expansion of
whole blood mononuclear cells and purified CD34+
cells from human umbilical cord blood. Hematologica
2004; 89: 606-607.
35. Abboud M, Xu F, LaVia M, et al. Study of early
hematopoietic precursors in human cord blood. Exp
Hematol 1992; 20: 1043-1047.
36. Sousa T, Sousa ME, Godinho MI, et al. Umbilical cord
blood processing: Volume reduction and recovery of
CD34+ cells. Bone Marrow Transplant 1997; 19: 311-
313.
37. Yang H, Acker JP, Hannon J, Miszta-Lane H, Akabutu
JJ, McGann LE. Damage and protection of UC blood
cells during cryopreservation. Cytotherapy 2001; 3:
377-386.

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