Name: Mesenchymal Stem Cell Surface Staining for Immunophenotyping
Uploaded: 2023-11-10T14:30:00
Description: Watch this Scientific Journal Video about Mesenchymal Stem Cell Surface Staining for Immunophenotyping at JoVE.com

mesenchymal stem cell surface staining for immunophenotyping

인간 중간엽 줄기 세포의 형광 활성화 단일 세포 분류

Mesenchymal stem cells (MSCs) can be regarded as a scalable source of cells suitable for cell-based therapies and may be considered a gold standard system in regenerative medicine. These cells can be isolated from a variety of sources in the body with different tissue origins1. Depending on their source tissue, each type of MSC displays an ambiguous in vitro behavior2. This is well observed in their morphological and functional properties3. Multiple studies have shown intra-clonal variation in dimensions, including adult tissue differentiation, genomic state, and metabolic and cellular architecture of MSCs2,4.
Immunophenotyping of cells has been a common application of flow cytometry for the identification of stem cells and this was&#160;utilized by the International Society for&#160;Cell and Gene Therapy (ISCT) in 2006 to prescribe a list of minimal criteria to identify cells as MSCs. It stated that along with plastic adherence and the ability to differentiate into three lineages (osteogenic, chondrogenic, and adipogenic) in vitro, &#8805;95% of the cell population must express CD105, CD73, CD90, and these cells must lack the expression (&#8804;2% positive) of CD34, CD45, CD11b, CD14, and HLA-DR, as measured by flow cytometry5. Although the MSCs were defined by a set of biomarkers under the minimal criteria of the ISCT, their immune properties could not be benchmarked with these biomarkers and there was a need for more beyond these criteria to make cross-study comparisons and clonal variations easier to quantify2.
Despite the guidelines set by ISCT, extensive research on MSCs has shown that heterogeneity exists in this population, which could arise due to a multitude of factors, mainly due to the ubiquitous nature of heterogeneity that arises between MSC donors6, tissue sources7, individual cells within a clonal population8, and culture conditions2,9,10. Characterization and purification of these primary cells from a variety of tissue sources to ensure quality and cell fate are key steps in their production. The need to understand the displayed variations amongst the population requires an efficient method to resolve it into subpopulations that can be divided and collected separately11. Single-cell level analyses help overcome the challenges of cell-cell variation, reduce biological noise arising from a heterogeneous population, and offer the ability to investigate and characterize rare cells12.
Based on the purpose and chosen parameters, several methods can be employed to sort and enrich the selected populations. Cell-sorting techniques can comprise both bulk sorting and single-cell sorting methods. While bulk sorting can enrich target populations through Magnetic-activated cell sorting (MACS)13, fractionation14, and elutriation15, single-cell sorting can enrich more homogeneous populations by means of fluorescence-activated cell sorting (FACS)11. A comparative analyses&#160;of each of these methods with its own set of advantages and disadvantages is highlighted in Table 1.
Table 1: Comparative analyses of different techniques:&#160;MACS, Fractionation, Elutriation, and FACS highlighting the differences in their principle and the advantages and disadvantages of choosing a particular technique over another. Abbreviations: MACS = Magnetic-activated cell sorting; FACS = Fluorescence-activated cell sorting. <a href="https://www.jove.com/files/ftp_upload/65723/65723_Table_1_.xlsx" target="_blank">Please click here to download this Table.</a>
Since the advent of the technique, single-cell flow cytometry has played a major role in enumeration16, detection, and characterization of a specific cell population in a heterogeneous sample17. Hewitt et al. in 2006 laid the foundation of automated cell sorting methodology to enhance the isolation of homogenous pools of differentiated human embryonic stem cells (hESCs)18. Single-cell sorting enriched the population of GFP-transduced hESCs facilitating the isolation of genetically modified clones, which opened a new dimension in clinical research. To improve the sort efficiency, two approaches have generally been taken; either the collection media of the sorted populations are modified to sustain viability and proliferation of post-sorted cells19 or the cell-sorting algorithm/software is appropriately modified12.
With the advancement of technology, commercial flow cytometers and cell sorters have been able to help address challenges that were met while aseptically sorting fragile and rare cell populations, especially stem cells of different origins.&#160;One of the major challenges of stem cell biologists has been the clonal isolation of human pluripotent stem cells following transfection protocols required in gene editing studies19. This was addressed by sorting single cells into 96-well plates that were coated with Mouse Embryonic Fibroblasts (MEFs) along with supplements and commercial small molecule ROCK inhibitors. However, cell isolation strategies could be largely refined with the use of index sorting, a feature of the sorting algorithm that identifies the immunophenotype of individual cells sorted12. This refined modality in single-cell sorting helped not only in enhancing sort efficiency for stem cells, especially with regard to rare hematopoietic stem cell populations, but also efficiently linked single-cell clones to their downstream functional assays20.
This paper focuses on single-cell sorting of immunophenotyped&#160;stem cells from human&#160;exfoliated deciduous teeth (SHEDs) for the enrichment of sub-populations to study their functional differentiation capacities. Using a combination of two MSC-positive markers, CD90 and CD73, and a negative hematopoietic marker CD45, the MSCs were immunophenotyped and the dim and null expressors were identified. Based on their immunophenotype the subpopulations were identified as pure MSCs, single positive and double negative populations. They were sorted using the single-cell sort mode to obtain pure and enriched subpopulations for further functional studies to identify whether the differential expression of markers was an artifact of in vitro culture conditions or whether it has any effect on the functional properties as well. Cells that were not homogeneous expressors of the &#34;positive MSC markers&#34; were sorted to study their functional properties.

저자 스포트라이트: 중간엽 줄기 세포의 정제된 집단을 분리하는 데 있어 단일 세포 분류의 중요성 

인간 박리 낙엽 치아에서 면역 표현형 중간엽 줄기 세포의 단일 세포 분류

This protocol details a crucial method for accurately characterizing and purifying human mesenchymal stem cells on a single platform, enabling efficient downstream applications like stem cell transplantation. It is particularly significant for clinical labs enhancing molecular and cytogenetic assays through precise single cell sorting of engineered or natural stem cells. The commonly used methods of isolation of purified stem cell populations refer to techniques such as immunomagnetic separation, density gradient, or microfluidic cell sorting.A technique like index sorting allows it to be linked to single cell RNA profiling that can extract transcriptomic information of each sorted cell. The key challenges involve maintaining sample quality, optimization of cell culture conditions, including cell density and viability during and after sorting is required. Additionally, choosing suitable nozzle sizes for the instrument and ensuring timely access to the sorters would also be considered.This protocol illustrates a precise staining panel for immunophenotyping and sorting the desired cell population. It ensures standardized sample quality, optimal cell viability, density for cell population sorting and define sorting experimental parameters on the FACSDiva software. This method enables a straightforward selection and immunophenotyping of stem cell population expressing specific biomarkers.This simple platform allows efficient sorting based on the target population aiding and obtaining purified samples for subsequent downstream applications.

Watch this Scientific Journal Video about Mesenchymal Stem Cell Surface Staining for Immunophenotyping at JoVE.com

Mesenchymal Stem Cell Surface Staining for Immunophenotyping  

면역표현형을 위한 중간엽 줄기세포 표면 염색

먼저 트립신화된 중간엽 줄기 세포를 300g에서 6분 동안 원심분리하여 세포 펠릿을 얻습니다. 다음으로, 세포 계수하기 전에 펠릿을 1밀리리터의 MSC 배지에 재현탁시킵니다. 세포 현탁액을 다시 원심분리한 다음, 상층액을 폐기한 후 적절한 부피의 염색 완충액에 펠릿을 재현탁시킵니다.보정 컨트롤을 준비하기 위해 7개의 팩스 튜브에 염색되지 않은 DAPI, V450, FITC, PE, PerCP-Cy5.5 및 APC로 레이블을 지정합니다. 다음으로, 보정을 위해 단일 염색 튜브를 준비하고 어둠 속에서 30분 동안 배양합니다. 배양 후 각 튜브의 세포를 두 번 세척하고 비드를 1mL의 염색 완충액으로 한 번 세척합니다.다음으로, 실온에서 10분 동안 200g의 와류 튜브를 원심분리합니다. 상층액을 버린 후 펠릿을 500마이크로리터의 염색 완충액에 재현탁시킵니다. DAPI 튜브를 섭씨 60도의 수조에서 5분 동안 배양한 다음 얼음 위에서 15분 동안 배양하여 염료의 포함을 유도합니다.현탁액에 5마이크로리터의 DAPI를 추가하고 획득할 때까지 배양합니다. 표에 따라 5개의 라벨이 부착된 팩스 튜브에 세포 및 항체 현탁액을 준비합니다. 배양 전에 튜브를 부드럽게 소용돌이치십시오.그런 다음 염색 완충액 1mL로 각 튜브를 두 번 세척합니다. 실온에서 10분 동안 200g의 와류 튜브를 원심분리한 다음 나머지 펠릿을 500마이크로리터의 염색 완충액에 다시 현탁시킵니다.

Research

JoVE Journal

Biology

Mesenchymal Stem Cell Surface Staining for Immunophenotyping

Single-Cell Sorting of Immunophenotyped Mesenchymal Stem Cells from Human Exfoliated Deciduous Teeth

The mesenchymal stem cells (MSCs) of an organism possess an extraordinary capacity to differentiate into multiple lineages of adult cells in the body and ...

연구

생물학

A Step-by-Step Guide for Seeding and Differentiation of Mesenchymal Stem Cell Cultures for Characterization

특성 분석을 위한 중간엽 줄기 세포 배양의 seeding 및 differentiation을 위한 단계별 가이드

Lineage-Specific Cytochemical Staining of Mesenchymal Stem Cells for Characterizing Differentiated Cells

분화된 세포의 특성화를 위한 중간엽 줄기세포의 계통 특이적 세포화학적 염색

Mesenchymal Stem Cell Sample Preparation, Flow Cytometric Analysis, and Cell Sorting

중간엽 줄기 세포 시료 전처리, 유세포 분석 및 세포 분류