In Vitro Cell Surface Marker Expression on Mesenchymal Stem Cell Cultures does not Reflect Their Ex Vivo Phenotype.

IF 4.5 3区 医学 Q2 CELL & TISSUE ENGINEERING
Stem Cell Reviews and Reports Pub Date : 2024-08-01 Epub Date: 2024-06-05 DOI:10.1007/s12015-024-10743-1
Ye Cao, Anna L Boss, Scott M Bolam, Jacob T Munro, Haemish Crawford, Nicola Dalbeth, Raewyn C Poulsen, Brya G Matthews
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Abstract

Cell surface marker expression is one of the criteria for defining human mesenchymal stem or stromal cells (MSC) in vitro. However, it is unclear if expression of markers including CD73 and CD90 reflects the in vivo origin of cultured cells. We evaluated expression of 15 putative MSC markers in primary cultured cells from periosteum and cartilage to determine whether expression of these markers reflects either the differentiation state of cultured cells or the self-renewal of in vivo populations. Cultured cells had universal and consistent expression of various putative stem cell markers including > 95% expression CD73, CD90 and PDPN in both periosteal and cartilage cultures. Altering the culture surface with extracellular matrix coatings had minimal effect on cell surface marker expression. Osteogenic differentiation led to loss of CD106 and CD146 expression, however CD73 and CD90 were retained in > 90% of cells. We sorted freshly isolated periosteal populations capable of CFU-F formation on the basis of CD90 expression in combination with CD34, CD73 and CD26. All primary cultures universally expressed CD73 and CD90 and lacked CD34, irrespective of the expression of these markers ex vivo indicating phenotypic convergence in vitro. We conclude that markers including CD73 and CD90 are acquired in vitro in most 'mesenchymal' cells capable of expansion. Overall, we demonstrate that in vitro expression of many cell surface markers in plastic-adherent cultures is unrelated to their expression prior to culture.

Abstract Image

间充质干细胞培养物的体外细胞表面标记表达并不反映其体内表型。
细胞表面标记物的表达是界定体外人类间充质干细胞或基质细胞(MSC)的标准之一。然而,包括 CD73 和 CD90 在内的标记物的表达是否能反映培养细胞的体内来源尚不清楚。我们评估了来自骨膜和软骨的原代培养细胞中 15 种推测的间充质干细胞标记物的表达,以确定这些标记物的表达是否反映了培养细胞的分化状态或体内细胞群的自我更新。在骨膜和软骨培养物中,培养细胞普遍一致地表达了各种假定的干细胞标记,其中CD73、CD90和PDPN的表达率均大于95%。用细胞外基质涂层改变培养表面对细胞表面标记表达的影响微乎其微。成骨分化导致 CD106 和 CD146 的表达丧失,但 CD73 和 CD90 在超过 90% 的细胞中得以保留。我们根据 CD90 与 CD34、CD73 和 CD26 的结合表达,对能形成 CFU-F 的新鲜分离骨膜细胞群进行了分类。所有原代培养物均普遍表达 CD73 和 CD90,而缺乏 CD34,与这些标记物在体内的表达无关,这表明表型在体外趋同。我们得出的结论是,大多数能够扩增的 "间充质 "细胞都能在体外获得包括 CD73 和 CD90 在内的标记物。总之,我们证明了许多细胞表面标记物在塑料粘附培养物中的体外表达与培养前的表达无关。
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来源期刊
Stem Cell Reviews and Reports
Stem Cell Reviews and Reports 医学-细胞生物学
CiteScore
9.30
自引率
4.20%
发文量
0
审稿时长
3 months
期刊介绍: The purpose of Stem Cell Reviews and Reports is to cover contemporary and emerging areas in stem cell research and regenerative medicine. The journal will consider for publication: i) solicited or unsolicited reviews of topical areas of stem cell biology that highlight, critique and synthesize recent important findings in the field. ii) full length and short reports presenting original experimental work. iii) translational stem cell studies describing results of clinical trials using stem cells as therapeutics. iv) papers focused on diseases of stem cells. v) hypothesis and commentary articles as opinion-based pieces in which authors can propose a new theory, interpretation of a controversial area in stem cell biology, or a stem cell biology question or paradigm. These articles contain more speculation than reviews, but they should be based on solid rationale. vi) protocols as peer-reviewed procedures that provide step-by-step descriptions, outlined in sufficient detail, so that both experts and novices can apply them to their own research. vii) letters to the editor and correspondence. In order to facilitate this exchange of scientific information and exciting novel ideas, the journal has created five thematic sections, focusing on: i) the role of adult stem cells in tissue regeneration; ii) progress in research on induced pluripotent stem cells, embryonic stem cells and mechanism governing embryogenesis and tissue development; iii) the role of microenvironment and extracellular microvesicles in directing the fate of stem cells; iv) mechanisms of stem cell trafficking, stem cell mobilization and homing with special emphasis on hematopoiesis; v) the role of stem cells in aging processes and cancerogenesis.
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