StemXVivo Mesenchymal Stem Cell Expansion Media Summary
A complete, fetal bovine serum-containing media formulated and optimized for the maintenance and expansion of purified human, mouse, and rat MSCs.
- Formulated to reduce variation
- All components, including fetal bovine serum, were selected and optimized for MSCs
- Ready to use
Why Culture MSCs in a Defined Medium?
Mesenchymal stem/stromal cells (MSCs) are a rare population of multipotent cells that can be derived from a number of tissues such as bone marrow, adipose, and placenta.
Given their rarity and sensitivity to ex vivo conditions, MSCs are most often expanded in vitro under specific culture conditions.
StemXVivo® MSC Expansion Media:
- Supports reproducible MSC growth in vitro.
- Can be supplemented with user-defined cytokines and growth factors, although these are not needed for culture
- Has been developed and optimized for use with human, mouse, and rat MSCs.
The term ‘mesenchymal stromal cells’ is commonly used to describe a heterogeneous population of cultured cells that are adherent to plastic, have a distinct morphology, and express a specific set of marker proteins. Within this heterogeneous population are cells referred to as ‘mesenchymal stem cells.’
Mesenchymal stem cells are multipotent, self-renewing cells that have the ability to differentiate into adipocytes, chondrocytes, and osteoblasts when cultured in vitro. Read More about MSC Nomenclature
StemXVivo® MSC Expansion Media Components
- Supplemented with sodium bicarbonate
- Does not contain antibiotics
2006 Proposed Change to MSC Nomenclature
Although mesenchymal stromal cells were once referred to as ‘mesenchymal stem cells’, a change to ‘mesenchymal stromal cells’ was proposed by the International Society for Cellular Therapy in 2006.1
The change in nomenclature originates from two important factors:
- Methods used to isolate mesenchymal stem cells yield a heterogeneous population of cells with only a fraction of these cells demonstrating multipotency.
- The absence of direct evidence that mesenchymal stem cells can self-renew and differentiate in vivo.
Use of Mesenchymal Stem and Stromal Cell Terminology
Data supporting MSC self-renewal and multipotency have been obtained using in vitro conditions, which does not adequately reflect the in vivo environment. The lack of in vivo data has led some researchers to question the validity of the term ‘mesenchymal stem cell’ providing further support for the use of ‘mesenchymal stromal cells’ to describe MSCs.2 While ‘mesenchymal stromal cells’ may be the more scientifically accurate term for MSCs, the two terms are often used interchangeably in the literature. R&D Systems recognizes the use of both mesenchymal stem cells and mesenchymal stromal cells and uses ‘MSC’ to indicate mesenchymal stem/stromal cells to account for both designations.
Definitions of Mesenchymal Stromal Cells and Mesenchymal Stem Cells
- Mesenchymal Stromal Cells – A heterogeneous population of cultured cells with similar characteristics such as the ability to adhere to plastic and the expression of specific marker proteins.
- Mesenchymal Stem Cells – A subpopulation of mesenchymal stromal cells that have the capacity to self-renew and differentiate into mesodermal lineages when cultured in vitro. The capacity to self-renew and differentiate in vivo has yet to be clearly demonstrated for mesenchymal stem cells.
- Dominici, M. et al. (2006) Cytotherapy 8:315.
- Keating, A. (2012) Cell Stem Cell 10:709.
Phenotypic Analysis of Human MSCs Expanded in StemXVivo® MSC Expansion Media. Human MSCs were expanded using StemXVivo®Mesenchymal Stem Cell (MSC) Expansion Media (Catalog # CCM004). Filled histograms indicate cells stained with markers of undifferentiated MSCs including anti-CD105 (Catalog # FAB10971P) or CD45 (Catalog # MAB1430). The open histograms show isotype-matched control staining. MSCs appropriately lack expression of CD45.
Phenotypic Analysis of Mouse MSCs Expanded in StemXVivo® MSC Expansion Media. Mouse MSCs were expanded using StemXVivo®Mesenchymal Stem Cell (MSC) Expansion Media (Catalog # CCM004). Filled histograms indicate cells stained with markers of undifferentiated MSCs including anti-CD44 (Catalog # AF6127) or CD45 (Catalog # MAB114). The open histograms show isotype-matched control staining. MSCs appropriately lack expression of CD45.
Refer to the product datasheet for complete product details.
Briefly, MSCs are cultured in expansion media using the following protocol:
- Plate MSCs in expansion media
- Culture MSCs to 80-90% confluency
- Passage MSCs using fresh expansion media
Reagents supplied in the StemXVivo® Mesenchymal Stem Cell Expansion Media (Catalog # CCM004):
- 250 mL of MSC expansion media
- Penicillin-Streptomycin (100X)
- Trypsin-EDTA (10X)
- Phosphate-Buffered Saline (PBS)
- MSCs (e.g., Rat Mesenchymal Stem Cells, Catalog # PSC003)
- 75 cm2 tissue culture flasks
- 15 mL centrifuge tubes
- Serological pipettes
- Pipettes and pipette tips
- 37 °C and 5% CO2 incubator
- Inverted microscope
- 2 °C to 8 °C refrigerator
- 37 °C water bath
This protocol has been tested using bone marrow- and/or adipose tissue-derived MSCs. If using a different tissue source or cell line, the protocol below may need to be modified.
Culturing Mesenchymal Stem Cells
Add 3.5 - 4.0 x 105 MSCs resuspended in 20 mL of the pre-warmed StemXVivo® MSC Expansion Media to a T75 flask.
Replace the medium every 3 days with fresh StemXVivo MSC Expansion Media.
Culture the MSCs to 80-90% confluency.
Subculturing Mesenchymal Stem Cells
Remove and discard the media from the T75 tissue culture flask(s) containing the MSCs.
Wash the cells with PBS.
Add 1-2 mL of pre-warmed trypsin to the MSCs and incubate the flask at 37 °C.
Transfer the dissociated MSCs to a 15 mL conical tube.
Centrifuge at 400 x g for 5 minutes.
Resuspend the cell pellet in 5 mL of StemXVivo® MSC Expansion Media.
Perform a cell count.
Add 3.5-4.0 x 105 MSCs resuspended in 20 mL of pre-warmed StemXVivo® MSC Expansion Media to each T75 flask.
Citations for StemXVivo Mesenchymal Stem Cell Expansion Media
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
Citations: Showing 1 - 10
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Biodegradable Poly-epsilon-Caprolactone Scaffolds with ECFCs and iMSCs for Tissue-Engineered Heart Valves
Authors: G Lutter, T Puehler, L Cyganek, J Seiler, A Rogler, T Herberth, P Knueppel, SN Gorb, J Sathananth, S Sellers, OJ Müller, D Frank, I Haben
International Journal of Molecular Sciences, 2022;23(1):. 2022
SIRT1-modified human umbilical cord mesenchymal stem cells ameliorate experimental peritoneal fibrosis by inhibiting the TGF-&beta/Smad3 pathway
Authors: Y Guo, L Wang, R Gou, Y Wang, X Shi, X Pang, L Tang
Stem Cell Res Ther, 2020;11(1):362. 2020
Identification of osteogenic progenitor cell-targeted peptides that augment bone formation
Authors: M Jiang, R Liu, L Liu, A Kot, X Liu, W Xiao, J Jia, Y Li, KS Lam, W Yao
Nat Commun, 2020;11(1):4278. 2020
SIRT1-modified human umbilical cord mesenchymal stem cells ameliorate experimental peritoneal fibrosis by inhibiting the TGF-beta/Smad3 pathway
Authors: Y Guo, L Wang, R Gou, Y Wang, X Shi, X Pang, L Tang
Stem Cell Res Ther, 2020;11(1):362. 2020
Metastatic renal cell carcinoma cells growing in 3D on poly?D?lysine or laminin present a stem?like phenotype and drug resistance
Authors: KK Brodaczews, ZF Bielecka, K Maliszewsk, C Szczylik, C Porta, E Bartnik, AM Czarnecka
Oncol. Rep., 2019;42(5):1878-1892. 2019
The Route by Which Intranasally Delivered Stem Cells Enter the Central Nervous System
Authors: C Galeano, Z Qiu, A Mishra, SL Farnsworth, JJ Hemmi, A Moreira, P Edenhoffer, PJ Hornsby
Cell Transplant, 2018;0(0):9636897187545. 2018
SIRT7 has a critical role in bone formation by regulating lysine acylation of SP7/Osterix
Authors: M Fukuda, T Yoshizawa, MF Karim, SU Sobuz, W Korogi, D Kobayasi, H Okanishi, M Tasaki, K Ono, T Sawa, Y Sato, M Chirifu, T Masuda, T Nakamura, H Tanoue, K Nakashima, Y Kobashigaw, H Morioka, E Bober, S Ohtsuki, Y Yamagata, Y Ando, Y Oike, N Araki, S Takeda, H Mizuta, K Yamagata
Nat Commun, 2018;9(1):2833. 2018
Increased insulin-like growth factor 1 production by polyploid adipose stem cells promotes growth of breast cancer cells
Authors: R Fajka-Boja, A Marton, A Tóth, P Blazsó, V Tubak, B Bálint, I Nagy, Z Heged?s, C Vizler, RL Katona
BMC Cancer, 2018;18(1):872. 2018
Bile acids induce hepatic differentiation of mesenchymal stem cells.
Authors: Sawitza I, Kordes C, Gotze S, Herebian D, Haussinger D
Sci Rep, 2015;5(0):13320. 2015
Intravenous and intratracheal mesenchymal stromal cell injection in a mouse model of pulmonary emphysema.
Authors: Tibboel, Jeroen, Keijzer, Richard, Reiss, Irwin, de Jongste, Johan C, Post, Martin
COPD, 2014;11(3):310-8. 2014
Skin-derived mesenchymal stem cells help restore function to ovaries in a premature ovarian failure mouse model.
Authors: Lai D, Wang F, Dong Z, Zhang Q
PLoS ONE, 2014;9(5):e98749. 2014
Dynamic microRNA profiles of hepatic differentiated human umbilical cord lining-derived mesenchymal stem cells.
Authors: Cui, Lina, Zhou, Xinmin, Li, Jinge, Wang, Liuyi, Wang, Jingbo, Li, Qiang, Chu, Jindong, Zheng, Linhua, Wu, Qiong, Han, Zheyi, Shi, Yongquan, Han, Ying, Fan, Daiming
PLoS ONE, 2012;7(9):e44737. 2012
Does StemXVivo® Mesenchymal Stem Cell Expansion Media need addition of serum before use?
The StemXVivo® Mesenchymal Stem Cell Expansion Media does not need addition of serum. Fetal bovine serum is included in the product, which is a complete medium and ready to use. The media may be supplemented with cytokine or growth factors for your desired cell culture application.
Does StemXVivo® Mesenchymal Stem Cell Expansion Media (Catalog # CCM004) contain Phenol Red?
Yes,StemXVivo® Mesenchymal Stem Cell Expansion Media contains Phenol Red.
How long can Mesenchymal Stem Cells (MSCs) be cultured in StemXVivo® Mesenchymal Stem Cell Expansion Media (Catalog # CCM004)?
MSCs can be grown to 80-90% confluency and subsequently subcultured using the protocol provided in the product datasheet. Researchers should establish the number of passages that is acceptable for their work. MSCs are sensitive to passsages and, if subcultured too many times, may start losing their MSC characteristics. Our MSC Functional Identification Kits can be used for validation of MSC mulitpotency.
Can Mesenchymal Stem Cells (MSCs) grown in StemXVivo® MSC Expansion Media (Catalog # CCM004) be cryopreserved?
MSCs grown in StemXVivo® MSC Expansion Media can be cryopreserved using appropriate cryopreservation media, such as StemXVivo® Serum-Free MSC Freezing Media (Catalog # CCM016) or equivalent.
Is it important to use medium without ribonucleosides and deoxyribonucleosides for growing mesenchymal stem cells?
We have not compared, in a side-by-side experiment, medium with and without ribonucleosides and deoxyribonucleosides for growing mesenchymal stem cells. There is literature to support the fact that using medium without ribonucleosides and deoxyribonucleosides is beneficial for growing mesenchymal stem cells.
Reviews for StemXVivo Mesenchymal Stem Cell Expansion Media
Average Rating: 4.5 (Based on 4 Reviews)
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I am working on bone marrow stem cells.StemXVivo MSC expansion medium help to retain the population doubling time from P-4 to P-8 30 hrs to 34 hrs only, where when I culture these MSC in normal alpha MEM after some time cells do not divide/proliferate.
I used this media for my umbilical cord-derived MSC, after speaking with a representative, who gave me a sample. I tried the product because I saw my cells were growing really small in another brand product. After switching, the rate of growth of my cells dramatically increased, and I could not be happier than that!