Stromal cell

Stromal cells, or mesenchymal stromal cells, are differentiating cells found in abundance within bone marrow but can also be seen all around the body. Stromal cells can become connective tissue cells of any organ, for example in the uterine mucosa (endometrium), prostate, bone marrow, lymph node and the ovary. They are cells that support the function of the parenchymal cells of that organ. The most common stromal cells include fibroblasts and pericytes. The term stromal comes from Latin stromat-, "bed covering", and Ancient Greek στρῶμα, strôma, "bed".

Stromal cells are an important part of the body's immune response and modulate inflammation through multiple pathways. They also aid in differentiation of hematopoietic cells and forming necessary blood elements. The interaction between stromal cells and tumor cells is known to play a major role in cancer growth and progression.[1] In addition, by regulating local cytokine networks (e.g. M-CSF,[2] LIF[3]), bone marrow stromal cells have been described to be involved in human hematopoiesis and inflammatory processes.

Stromal cells (in the dermis layer) adjacent to the epidermis (the top layer of the skin) release growth factors that promote cell division. This keeps the epidermis regenerating from the bottom while the top layer of cells on the epidermis are constantly being "sloughed" off the body. Additionally, stromal cells play a role in inflammation responses, and controlling the amount of cells accumulating at an inflamed region of tissue.[4]

Defining a Stromal Cell

Defining a stromal cell is of importance because it was a source of difficulty in the past. Without a strong definition studies could not cross over or gain knowledge from each other because a stromal cell was not well defined and went by a plethora of names. A stromal cell is currently more specifically referred to as a mesenchymal stem cell (MSC). It is non-hematopoietic, multipotent, and self-replicating.[5] These factors make it an effective tool in potential cell therapies and tissue repair. Being a mesenchymal cell indicates an ability to develop into various other cell types and tissues such as connective tissue, blood vessels, and lymphatic tissue.[5] Some stromal cells can be considered stem cells but not all therefore it can not be broadly termed a stem cell. All MSC have the ability adhere to plastic and replicate by themselves. MSC's have cell surface markers, but there are no universal list of the markers they are required to possess. There are typically a differentiation of CD73, CD90, CD105, CD44 as well as others that cover the cells surface. They also lack the expression of markers CD14, CD34, CD45, which can be important in the ability of stromal cells to remain fairly undetected by the immune system. Low levels of human leukocyte antigen (HLA-DR) make MSC's hypoimmunogenic.[6] MSC's have trilineage differentiation where they are able to adapt into osteoblast, chondrocytes, and adipocytes.[5] They can also display anti-inflammatory as well as proinflammatory responses allowing for the potential to help with a broad range of immune disorders and inflammatory diseases.

Sources of stromal cells

It is well known that stromal cells arise and are stored in the bone marrow until maturation and differentiation. They are located in the stroma and aid hematopoietic cells in forming the elements of the blood.[7] While a majority is found in the bone marrow scientists now know that stromal cells can be found in a variety of different tissues as well. These can include adipose tissue, endometrium, synovial fluid, dental tissue, amniotic membrane and fluid, as well as the placenta. Some of the most reliable stromal cells are located in the placenta because stromal cells age as we age.[7] The older we get the weaker our MSC's are, and the less applicable they are to be used as treatment.

Immunomodulatory Effects

In Cancer

During normal wound healing processes, the local stromal cells change into reactive stroma after altering their phenotype. However, under certain conditions, tumor cells can convert these reactive stromal cells further and transition them into tumor-associated stromal cells (TASCs).[8] In comparison to non-reactive stromal cells, TASCs secrete increased levels of proteins and matrix metalloproteinases (MMPs). These proteins include fibroblast activating protein and alpha-smooth muscle actin. Furthermore, TASCs secrete many pro-tumorigenic factors such as vascular endothelial growth factor (VEGF), stromal-derived factor-1 alpha, IL-6, IL-8, tenascin-C, and others. These factors are known to recruit additional tumor and pro-tumorigenic cells. The cross-talk between the host stroma and tumor cells is essential for tumor growth and progression. Tumor stromal production exhibits similar qualities as normal wound repair such as new blood vessel formation, immune cell and fibroblast infiltration, and considerable remodeling of the extracellular matrix. Additionally, the recruitment of local normal host stromal cells, such as bone marrow mesenchymal stromal cells, endothelial cells, and adipocytes, help create a conspicuously heterogeneous composition.[8] Furthermore, these cells secrete an abundance of factors that help regulate tumor development. Potential targets for tumor-associated stromal cell recruitment have been identified in the following host tissue: bone marrow, connective tissue, adipose tissue, and blood vessels. Moreover, evidence suggests that tumor-associated stroma are a prerequisite for metastasis and tumor cell invasion. These are known to arise from at least six different origins: immune cells, macrophages, adipocytes, fibroblasts, pericytes, and bone marrow mesenchymal stromal cells.[8]

Anti-inflammation

An important ability of MSC's are their ability to suppress an excessive immune response. T-cells, B-cells, dendritic cells, macrophages, and natural killer cells can be overstimulated by the immune systems response, but stromal cells help to keep the balance and make sure the body can properly heal without an excessive amount of inflammation.

MSC's release immunosuppressive mediators when an inflammatory response is stimulated. The mechanisms can include nitric oxide (NO), indoleamine 2,3-dioxygenase (IDO), prostaglandin E2 (PGE2), programmed death of ligand 1 (PD-L1) and many more.[5] Without MSC's these factors are extremely limited and cause the immune response to happen quickly and without obstacles. However, without regulation there can be an overstimulation of the immune response and that is when MSC's and their released factors are necessary. IFN-gamma stimulates the presence of MSC's expressing IDO. The IDO catalyzes the conversion of tryptophan into kynurenine inhibiting the T-cells from further generation.[5] The mechanism that utilizes NO also decreases T-cell proliferation by not allowing monocytes to mature. Immature monocytes remain as dendritic cells which leads to fewer T-cells being activated, and a positive feedback loop increases IL-10 levels so the dendritic cells adopt a more anti-inflammatory phenotype.[5]

MSC's specifically target the effector arm of T-cells and therefore can suppress the immune systems response to some degree.[9] Dendritic cells in the presence of MSC's are immature and undifferentiated which causes impaired function to call upon T-cells and bridge the gap between the innate and adaptive immune responses.[10] These dendritic cells instead release cytokines in order to regulate the growth and activity of other immune system cells as well as blood cells.[11]

When there is a high level of MSC's during an immune response the generation of more B-cells is stunted. The B-cells that can still be produced are impacted by diminished antibody count production and chemotactic behavior. This reduction in B-cell proliferation is caused by the presence of IFN-gamma, stimulating IDO on the surface of MSC's and suppressing effector cells through the tryptophan pathway.[6]

Proinflammation

Stromal cells are most often looked at for their hypoimmunogenic response but they are actually non specific immunomodulating. MSC's can flip the switch between anti-inflammatory and proinflammatory based on their levels of IFN-gamma, TNF-alpha, and either +IL-6 or -IL-6.[12] Pathogens are initially recognized by toll-like receptors (TLR's). This triggers inflammatory mediators and activates either pro or anti inflammatory MSC's.[13] If IFN-gamma and TNF-alpha are present in high levels the MSC will stimulate an anti-inflammatory response by activating CD4, CD25, FoxP3, and Treg cell instead of T-cells. However, if the levels of IFN-gamma and TNF-alpha are low the MSC's produce low levels of IDO and therefore can activate T-cells normally and the inflammation process takes place.[12] MSC's with +IL-6 in the presence of monocytes forms M2 and CCL-18 which inhibits T-cells from being activated. However, MSC's with -IL-6 in the presence of monocytes form M1 and can activate T-cells and produce high levels of IFN-gamma and TNF-alpha which regulates the inflammation through the previously mentioned mechanism.[12]

Role in Hematopoiesis

Before differentiation a majority of MSC's are housed within the bone marrow which is also where lymphocytes and other blood elements are formed. Stromal cells play a large role in the distinction of hematopoietic cells (cells that can differentiate into other blood cells).[14] MSC's act as a physical support for differentiating hematopoietic cells in conjunction with the extracellular matrix. Stromal cells also provide nutrients and growth factors for the hematopoietic cell to continue to develop. Lastly, MSC's express adhesion molecules that influence the hematopoietic cells differentiation.[14] The body tells the MSC's what blood elements are needed and it conveys those adhesion molecules to the differentiating cell.[15]  

Furthermore, the tumor stroma is primarily composed of the basement membrane, fibroblasts, extracellular matrix, immune cells, and blood vessels. Typically, most host cells in the stroma are characterized by tumor-suppressive abilities. However, during malignancy, the stroma will undergo alterations to consequently incite growth, invasion, and metastasis. These changes include the formation of carcinoma-associated fibroblasts (CAFs) which comprises a major portion of the reactive tissue stroma and plays a critical role in regulating tumor progression.[16]

Certain types of skin cancers (basal cell carcinomas) cannot spread throughout the body because the cancer cells require nearby stromal cells to continue their division. The loss of these stromal growth factors when the cancer moves throughout the body prevents the cancer from invading other organs.

Stroma is made up of the non-malignant cells, but can provide an extracellular matrix on which tumor cells can grow. Stromal cells may also limit T-cell proliferation via nitric oxide production, hindering immune capability.[17]

Use in Future Therapies

MSC's have the potential to be used in multiple disease interventions. One important feature of MSC's is that they can go virtually undetected by the immune system. The stromal cells possess serine proteases which are an inhibitor of the immune response. They also do not carry receptors that relate to the immune system or are not in high enough concentrations to admit a response.[18] This is helpful for the future of MSC cell therapies because there will be little to no negative effects from a possible immune response. There is promising research in the fields of autoimmune disorders such as multiple sclerosis and rheumatoid arthritis as well as wound healing, COPD, and even acute respiratory distress syndrome[19] (an effect of COVID-19). Stromal cells have the unique ability to create an immune modulated environment in order to best respond to foreign and known particles.[20] The reason for halted use of MSC's is the lack of knowledge of the cells in vivo. Most research of these cells have been done in controlled laboratory environments which can sometimes alter the effects seen.[21] The potentials, however, for cell therapy in tissue repair, immune modulation, and anti-tumor agent distribution are promising.[21]

See also

References

  1. ↑ Wiseman BS, Werb Z (May 2002). "Stromal effects on mammary gland development and breast cancer" (PDF). Science. 296 (5570): 1046–9. Bibcode:2002Sci...296.1046W. doi:10.1126/science.1067431. PMC 2788989. PMID 12004111. Archived from the original (PDF) on 2010-06-28.
  2. ↑ Fixe P, Rougier F, Ostyn E, Gachard N, Faucher JL, Praloran V, Denizot Y (March 1997). "Spontaneous and inducible production of macrophage colony-stimulating factor by human bone marrow stromal cells". European Cytokine Network. 8 (1): 91–5. PMID 9110154.
  3. ↑ Lorgeot V, Rougier F, Fixe P, Cornu E, Praloran V, Denizot Y (October 1997). "Spontaneous and inducible production of leukaemia inhibitory factor by human bone marrow stromal cells". Cytokine. 9 (10): 754–8. doi:10.1006/cyto.1997.0225. PMID 9344507.
  4. ↑ Buckley CD, Barone F, Nayar S, Bénézech C, Caamaño J (2015). "Stromal cells in chronic inflammation and tertiary lymphoid organ formation". Annual Review of Immunology. 33: 715–45. doi:10.1146/annurev-immunol-032713-120252. PMID 25861980.
  5. 1 2 3 4 5 6 "What are Stromal Cells (Mesenchymal Stem Cells)?". News-Medical.net. 2019-01-04. Retrieved 2020-12-01.
  6. 1 2 Nauta, Alma J.; Fibbe, Willem E. (2007-11-15). "Immunomodulatory properties of mesenchymal stromal cells". Blood. 110 (10): 3499–3506. doi:10.1182/blood-2007-02-069716. ISSN 0006-4971. PMID 17664353.
  7. 1 2 Ullah, Imran; Subbarao, Raghavendra Baregundi; Rho, Gyu Jin (2015-04-28). "Human mesenchymal stem cells - current trends and future prospective". Bioscience Reports. 35 (2). doi:10.1042/BSR20150025. ISSN 0144-8463. PMC 4413017. PMID 25797907.
  8. 1 2 3 Bussard KM, Mutkus L, Stumpf K, Gomez-Manzano C, Marini FC (August 2016). "Tumor-associated stromal cells as key contributors to the tumor microenvironment". Breast Cancer Research. 18 (1): 84. doi:10.1186/s13058-016-0740-2. PMC 4982339. PMID 27515302.
  9. ↑ Alberts, Bruce; Johnson, Alexander; Lewis, Julian; Raff, Martin; Roberts, Keith; Walter, Peter (2002). "T Cells and MHC Proteins". Molecular Biology of the Cell. 4th Edition.
  10. ↑ Zhou, Haibo; Wu, Li (July 2017). "The development and function of dendritic cell populations and their regulation by miRNAs". Protein & Cell. 8 (7): 501–513. doi:10.1007/s13238-017-0398-2. ISSN 1674-800X. PMC 5498339. PMID 28364278.
  11. ↑ Park, Chae Woon; Kim, Keun-Soo; Bae, Sohyun; Son, Hye Kyeong; Myung, Pyung-Keun; Hong, Hyo Jeong; Kim, Hoeon (May 2009). "Cytokine Secretion Profiling of Human Mesenchymal Stem Cells by Antibody Array". International Journal of Stem Cells. 2 (1): 59–68. doi:10.15283/ijsc.2009.2.1.59. ISSN 2005-3606. PMC 4021795. PMID 24855521.
  12. 1 2 3 Bernardo, Maria Ester; Fibbe, Willem E. (2013-10-03). "Mesenchymal Stromal Cells: Sensors and Switchers of Inflammation". Cell Stem Cell. 13 (4): 392–402. doi:10.1016/j.stem.2013.09.006. ISSN 1934-5909. PMID 24094322.
  13. ↑ Takeda, Kiyoshi; Kaisho, Tsuneyasu; Akira, Shizuo (April 2003). "Toll-Likereceptors". Annual Review of Immunology. 21 (1): 335–376. doi:10.1146/annurev.immunol.21.120601.141126. ISSN 0732-0582. PMID 12524386.
  14. 1 2 Bianco, Paolo; Robey, Pamela Gehron (2000-06-15). "Marrow stromal stem cells". The Journal of Clinical Investigation. 105 (12): 1663–1668. doi:10.1172/JCI10413. ISSN 0021-9738. PMC 378520. PMID 10862779.
  15. ↑ Morrison, Sean J.; Uchida, Nobuko; Weissman, Irving L. (November 1995). "The Biology of Hematopoietic Stem Cells". Annual Review of Cell and Developmental Biology. 11 (1): 43–45. doi:10.1146/annurev.cb.11.110195.000343. ISSN 1081-0706.
  16. ↑ Bremnes RM, Dønnem T, Al-Saad S, Al-Shibli K, Andersen S, Sirera R, et al. (January 2011). "The role of tumor stroma in cancer progression and prognosis: emphasis on carcinoma-associated fibroblasts and non-small cell lung cancer". Journal of Thoracic Oncology. 6 (1): 209–17. doi:10.1097/JTO.0b013e3181f8a1bd. PMID 21107292. S2CID 19822350.
  17. ↑ Lukacs-Kornek V, Malhotra D, Fletcher AL, Acton SE, Elpek KG, Tayalia P, et al. (September 2011). "Regulated release of nitric oxide by nonhematopoietic stroma controls expansion of the activated T cell pool in lymph nodes". Nature Immunology. 12 (11): 1096–104. doi:10.1038/ni.2112. PMC 3457791. PMID 21926986.
  18. ↑ Luzzani, C.; Miriuka, S. G. (2017-01-01), Bolontrade, Marcela F.; García, Mariana G. (eds.), "4 - Mesenchymal Stem/Stromal Cells Derived From Pluripotent Stem Cells", Mesenchymal Stromal Cells as Tumor Stromal Modulators, Boston: Academic Press, pp. 103–119, ISBN 978-0-12-803102-5, retrieved 2020-12-03
  19. ↑ Rada, Gabriel; Corbalán, Javiera; Rojas, Patricio (2020-04-18). "Mesenchymal stromal cells for COVID-19: A living systematic review protocol". dx.doi.org. doi:10.1101/2020.04.13.20064162. S2CID 216055266. Retrieved 2020-12-01.
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  21. 1 2 Horwitz, Edwin M.; Andreef, Michael; Frassoni, Francesco (November 2006). "Mesenchymal Stromal Cells". Current Opinion in Hematology. 13 (6): 419–425. doi:10.1097/01.moh.0000245697.54887.6f. ISSN 1065-6251. PMC 3365862. PMID 17053453.
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