Bone Marrow CD۳۴ Positive Cells May Be Suitablefor Collection after Death

  • سال انتشار: 1401
  • محل انتشار: بیست و سومین کنگره بین المللی هیبریدی پزشکی تولید مثل و هجدهمین کنگره هیبریدی فناوری سلولهای بنیادی رویان
  • کد COI اختصاصی: RROYAN23_283
  • زبان مقاله: انگلیسی
  • تعداد مشاهده: 207
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نویسندگان

A Rafat

Department of Anatomical Sciences, Faculty of Medicine, TabrizUniversity of Medical Sciences, Tabriz, Iran

KH Dizaji Asl

Department of Anatomical Sciences, Faculty of Medicine, TabrizUniversity of Medical Sciences, Tabriz, Iran

Z Mazloumi

Department of Applied Cell Sciences, Faculty of Advanced MedicalSciences, Tabriz University of Medical Sciences, Tabriz, Iran

H Nozad Charoudeh

S tem Cell Research Center, Tabriz University of Medical Sciences,Tabriz, Iran

چکیده

Objective: Hematopoietic s tem cells (HSCs) which are characterizedwith CD۳۴+ phenotype, have a pivotal role in bloodcell regeneration. They are located in lowes t hypoxic areas inthe bone marrow niches. This microenvironment protects themfrom DNA damage and excessive proliferation, whereas the oxygenatedarea driving cells out of quiescent s tate into proliferation.Given the resis tance of HSCs to hypoxia, it is reasonableto imagine that they can survive for some time in the absenceof oxygen.Materials and Methods: Here, we evaluated CD۳۴, Bax, Bcl-۲, Bcl-xl, and p۵۳ genes expression after death. Moreover, wees tablished the ex-vivo development of HSCs using SCF, FLT۳,IL-۲, and IL-۱۵ cytokines in culture sys tem.Results: Our finding indicated that although the mos t of thedead person's mononuclear cells were alive and adequately expressedthe CD۳۴ on their surfaces at the firs t day of isolation,the viability and CD۳۴+/Ki-۶۷ expression declined significantlyafter culture process.Conclusion: Taken together, our finding indicated that the viabilityand CD۳۴+ expression was acceptable on day ۰ and couldbe used as a novel method for therapeutic purposes

کلیدواژه ها

CD۳۴ Marker, Death Individual, HematopoieticS tem Cells (HSCs), Oxygen Tension

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