Cited by 504Hematopoietic Stem Cell TransplantationT-cell and B-cell ImmunologyMesenchymal stem cell research

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Regulation of Hemopoiesis by Bone Marrow Stromal Cells and Their Products

Dorshkind, Kenneth·1990·Annual Review of Immunology

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Abstract

Exhausted CD8 T (Tex) cells are a distinct cell lineage that arise during chronic infections and cancers in animal models and humans. Tex cells are characterized by progressive loss of effector functions, high and sustained inhibitory receptor expression, ...Read More

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Crossref · 10.1146/annurev.iy.08.040190.000551

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STROMAL CELLS RESPONSIBLE FOR TRANSFERRING THE MICROENVIRONMENT OF THE HEMOPOIETIC TISSUES
Friedenstein, A. J., Chailakhyan, R. K., Latsinik, N. V., Panasyuk, A. F., & Keilis-Borok, I. V. (1974) · Transplantation · doi:10.1097/00007890-197404000-00001 · Cited by 1,433
The proto-oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the mouse W locus
Chabot, B., Stephenson, D. A., Chapman, V. M., Besmer, P., & Bernstein, A. (1988) · Nature · doi:10.1038/335088a0 · Cited by 1,339
The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene
Geissler, E. N., Ryan, M. A., & Housman, D. E. (1988) · Cell · doi:10.1016/0092-8674(88)90020-7 · Cited by 1,287
Production of hybridoma growth factor by human monocytes
Aarden, L. A., de Groot, E. R., Schaap, O. L., & Lansdorp, P. M. (1987) · European Journal of Immunology · doi:10.1002/eji.1830171004 · Cited by 1,091
Hereditary Anemias of the Mouse: A Review for Geneticists
Russell, E. S. (1979) · Advances in genetics · doi:10.1016/s0065-2660(08)60549-0 · Cited by 1,083
The molecular control of cell division, differentiation commitment and maturation in haemopoietic cells
Metcalf, D. (1989) · Nature · doi:10.1038/339027a0 · Cited by 1,023
A STOCHASTIC MODEL OF STEM CELL PROLIFERATION, BASED ON THE GROWTH OF SPLEEN COLONY-FORMING CELLS
Till, J. E., McCulloch, E. A., & Siminovitch, L. (1964) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.51.1.29 · Cited by 911
Heparan sulphate bound growth factors: a mechanism for stromal cell mediated haemopoiesis
Roberts, R. A., Gallagher, J. T., Spooncer, E., Alien, T. D., Bloomfield, F. H., & Dexter, T. M. (1988) · Nature · doi:10.1038/332376a0 · Cited by 804
Tumor necrosis factor/cachectin interacts with endothelial cell receptors to induce release of interleukin 1.
Nawroth, P. P., Bank, I., Handley, D. A., Cassimeris, J., Chess, L., & Stern, D. (1986) · The Journal of Experimental Medicine · doi:10.1084/jem.163.6.1363 · Cited by 692
Long-term culture of human bone marrow cells.
Gartner, S., & Kaplan, H. S. (1980) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.77.8.4756 · Cited by 611

Show all 100 references

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Cell circuits between B cell progenitors and IL-7+ mesenchymal progenitor cells control B cell development
Fistonich, C., Zehentmeier, S., Bednarski, J. J., Miao, R., Schjerven, H., Sleckman, B. P., & Pereira, J. P. (2018) · The Journal of Experimental Medicine · doi:10.1084/jem.20180778 · Cited by 91
Barrier cells: stromal regulation of hematopoiesis and blood cell release in normal and stressed murine bone marrow
Weiss, L., & Geduldig, U. (1991) · Blood · doi:10.1182/blood.v78.4.975.975 · Cited by 91
The role of bone marrow microenvironment (BMM) cells in acute myeloid leukemia (AML) progression: immune checkpoints, metabolic checkpoints, and signaling pathways
Bakhtiyari, M., Liaghat, M., Aziziyan, F., Shapourian, H., Yahyazadeh, S., Alipour, M., Shahveh, S., Maleki‐Sheikhabadi, F., Halimi, H., Forghaniesfidvajani, R., et al. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-023-01282-2 · Cited by 93
Influence of cellular microenvironment and paracrine signals on chondrogenic differentiation
Grässel, S. (2007) · Frontiers in bioscience · doi:10.2741/2440 · Cited by 87
VLA‐4 antagonists: Potent inhibitors of lymphocyte migration
Yang, G. X. Q., & Hagmann, W. K. (2003) · Medicinal Research Reviews · doi:10.1002/med.10044 · Cited by 87
Immunoglobulin recombinase gene activity is modulated reciprocally by interleukin 7 and CD19 in B cell progenitors.
Billips, L. G., Núnêz, C., Bertrand, F. E., Stanković, A. K., Gartland, G. L., Burrows, P. D., & Cooper, M. D. (1995) · The Journal of Experimental Medicine · doi:10.1084/jem.182.4.973 · Cited by 86
Alternate splicing of mRNAs encoding human mast cell growth factor and localization of the gene to chromosome 12q22-q24.
Anderson, D. M., Williams, D. E., Tushinski, R. J., Gimpel, S. D., Eisenman, J. R., Cannizzaro, L. A., Aronson, M. M., Croce, C. M., Huebner, K., & Cosman, D. J. (1991) · PubMed · Cited by 85
Bone Marrow Osteoblastic Niche: A New Model to Study Physiological Regulation of Megakaryopoiesis
Pallotta, I., Lovett, M. L., Rice, W., Kaplan, D. L., & Balduini, A. (2009) · PLoS ONE · doi:10.1371/journal.pone.0008359 · Cited by 84
Ex vivo culture with human brain endothelial cells increases the SCID-repopulating capacity of adult human bone marrow
Chute, J. P., Saini, A., Chute, D. J., Wells, M. R., Clark, W. B., Harlan, D. M., Park, J. R., Stull, M. K., Civin, C. I., & Davis, T. A. (2002) · Blood · doi:10.1182/blood-2002-04-1238 · Cited by 84
The Role of Hyaluronic Acid in Hemopoietic Stem Cell Biology
Haylock, D. N., & Nilsson, S. K. (2006) · Regenerative Medicine · doi:10.2217/17460751.1.4.437 · Cited by 86
Physiological specialisation of adipose tissue
Pond, C. M. (1999) · Progress in Lipid Research · doi:10.1016/s0163-7827(99)00003-x · Cited by 84
Optical Imaging of PKH‐Labeled Hematopoietic Cells in Recipient Bone Marrow In Vivo
Askenasy, N., & Farkas, D. L. (2002) · Stem Cells · doi:10.1634/stemcells.20-6-501 · Cited by 84
Establishment and characterization of cloned human thymic epithelial cell lines—Analysis of adhesion molecule expression and cytokine production
Fernandez, E., Vicente, A., Zapata, A., Brera, B., Lozano, J., Martinez, C., & Toribio, M. (1994) · Blood · doi:10.1182/blood.v83.11.3245.3245 · Cited by 84
Does habitat fragmentation cause stress in the agile antechinus? A haematological approach
Johnstone, C. P., Lill, A., & Reina, R. D. (2011) · Journal of Comparative Physiology B · doi:10.1007/s00360-011-0598-7 · Cited by 83
Effects of synergistic cytokine combinations, low oxygen, and irradiated stroma on the expansion of human cord blood progenitors
Koller, M. R., Bender, J., Papoutsakis, E., & Miller, W. (1992) · Blood · doi:10.1182/blood.v80.2.403.403 · Cited by 83
Collagen type VI in the human bone marrow microenvironment: a strong cytoadhesive component
Klein, G., Muller, C., Tillet, E., Ml, C., & Timpl, R. (1995) · Blood · doi:10.1182/blood.v86.5.1740.bloodjournal8651740 · Cited by 82
Therapeutic Implications of Mesenchymal Stem Cells in Liver Injury
Puglisi, M. A., Tesori, V., Lattanzi, W., Piscaglia, A. C., Gasbarrini, G. B., D’Ugo, D., & Gasbarrini, A. (2011) · BioMed Research International · doi:10.1155/2011/860578 · Cited by 81
The Development of B Cells in the Bone Marrow Is Controlled by the Balance between Cell-Autonomous Mechanisms and Signals from the Microenvironment
Carsetti, R. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.191.1.5 · Cited by 80
Platelets and Stromal Cell-Derived Factor-1 in Progenitor Cell Recruitment
Stellos, K., & Gawaz, M. (2007) · Seminars in Thrombosis and Hemostasis · doi:10.1055/s-2007-969029 · Cited by 79
Connexin-43-type gap junctions mediate communication between bone marrow stromal cells
Dorshkind, K. A., Green, L., Godwin, A. K., & Fletcher, W. (1993) · Blood · doi:10.1182/blood.v82.1.38.bloodjournal82138 · Cited by 79
Cell circuits and niches controlling B cell development
Zehentmeier, S., & Pereira, J. P. (2019) · Immunological Reviews · doi:10.1111/imr.12749 · Cited by 83
Long-term culture system for selective growth of human B-cell progenitors.
Rawlings, D. J., Quan, S. G., Kato, R. M., & Witte, O. N. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.5.1570 · Cited by 76
N-cadherin is developmentally regulated and functionally involved in early hematopoietic cell differentiation
Puch, S., Armeanu, S., Kibler, C., Johnson, K. R., Müller, C. A., Wheelock, M. J., & Klein, G. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.8.1567 · Cited by 77
CXCR4 chemokine receptors (CD184) and α4β1 integrins mediate spontaneous migration of human CD34+ progenitors and acute myeloid leukaemia cells beneath marrow stromal cells (pseudoemperipolesis)
Burger, J. A., Spoo, A. C., Dwenger, A., Burger, M., & Behringer, D. M. (2003) · British Journal of Haematology · doi:10.1046/j.1365-2141.2003.04466.x · Cited by 77
Secretion of cytokines (interleukins-1 alpha, -3, and -6 and granulocyte-macrophage colony-stimulating factor) by normal human bone marrow megakaryocytes
Wickenhauser, C., Lorenzen, J., Thiele, J., Hillienhof, A., Jungheim, K., Schmitz, B., Hansmann, M., & Fischer, R. (1995) · Blood · doi:10.1182/blood.v85.3.685.bloodjournal853685 · Cited by 77
Proliferation of Bone Marrow Pro-B Cells Is Dependent on Stimulation by the Pituitary/Thyroid Axis
Foster, M. P., Montecino-Rodriguez, E., & Dorshkind, K. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.163.11.5883 · Cited by 75
CD19 and BAFF‐R can signal to promote B‐cell survival in the absence of Syk
Hobeika, E., Levit‐Zerdoun, E., Anastasopoulou, V., Pohlmeyer, R., Altmeier, S., Alsadeq, A., Dobenecker, M., Pelanda, R., & Reth, M. G. (2015) · The EMBO Journal · doi:10.15252/embj.201489732 · Cited by 74
Hyaluronan Increases RANKL Expression in Bone Marrow Stromal Cells Through CD44
Cao, J., Singleton, P. A., Majumdar, S., Boudignon, B. M., Burghardt, A. J., Kurimoto, P., Wronski, T. J., Bourguignon, L., & Halloran, B. P. (2005) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.041014 · Cited by 79
Vascular cell adhesion molecule 1-positive reticular cells express interleukin-7 and stem cell factor in the bone marrow
Funk, P. E., Stephan, R., & Witte, P. (1995) · Blood · doi:10.1182/blood.v86.7.2661.2661 · Cited by 74
Cell-specific activation and detoxification of benzene metabolites in mouse and human bone marrow: identification of target cells and a potential role for modulation of apoptosis in benzene toxicity.
Ross, D., Siegel, D. M., Schattenberg, D. G., Sun, X. M., & Moran, J. L. (1996) · Environmental Health Perspectives · doi:10.1289/ehp.961041177 · Cited by 73
E-cadherin is functionally involved in the maturation of the erythroid lineage.
Armeanu, S., Bühring, H., Reuss-Borst, M. A., Müller, C. A., & Klein, G. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.131.1.243 · Cited by 73
Engineering a mimicry of bone marrow tissue ex vivo
Panoskaltsis, N., Mantalaris, A., & Wu, J. (2005) · Journal of Bioscience and Bioengineering · doi:10.1263/jbb.100.28 · Cited by 71
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Itakura, S., Asari, S., Rawson, J., Ito, T., Todorov, I., Liu, C., Sasakic, N., KANDEEL, F. R., & Mullen, Y. (2007) · American Journal of Transplantation · doi:10.1111/j.1600-6143.2006.01643.x · Cited by 71
Downregulation of tenascin expression by glucocorticoids in bone marrow stromal cells and in fibroblasts.
Ekblom, M., Fässler, R., Tomasini-Johansson, B. R., Nilsson, K., & Ekblom, P. (1993) · The Journal of Cell Biology · doi:10.1083/jcb.123.4.1037 · Cited by 71
Phenotypic and Functional Comparison of Mesenchymal Stem Cells Derived from the Bone Marrow of Normal Adults and Patients with Hematologic Malignant Diseases
Zhao, Z.-G., Liang, Y., Li, K., Li, W., Li, Q.-B., Chen, Z.-C., & Zou, P. (2007) · Stem Cells and Development · doi:10.1089/scd.2007.0008 · Cited by 70
Unusual patterns of immunoglobulin gene rearrangement and expression during human B cell ontogeny: human B cells can simultaneously express cell surface kappa and lambda light chains.
Pauza, M. E., Rehmann, J. A., & LeBien, T. W. (1993) · The Journal of Experimental Medicine · doi:10.1084/jem.178.1.139 · Cited by 69
Perspectives on the Morphology and Biology of CD34-Negative Stem Cells
Huss, R. (2000) · Stem Cells and Development · doi:10.1089/152581600750062228 · Cited by 68
Simultaneous activation of p53 and inhibition of XIAP enhance the activation of apoptosis signaling pathways in AML
Carter, B. Z., Mak, D. H. F., Schober, W. D., Koller, E., Pinilla, C., Vassilev, L. T., Reed, J. C., & Andreeff, M. (2009) · Blood · doi:10.1182/blood-2009-03-212563 · Cited by 67
Porcine brain microvascular endothelial cells support the in vitro expansion of human primitive hematopoietic bone marrow progenitor cells with a high replating potential: requirement for cell-to-cell interactions and colony-stimulating factors
Davis, T., Dh, R., Lee, K. P., & Kessler, S. (1995) · Blood · doi:10.1182/blood.v85.7.1751.bloodjournal8571751 · Cited by 67
Hematopoietic Stem Cells in the Mouse Embryonic Yolk Sac
Auerbach, R., Huang, H., & Lü, L. (1996) · Stem Cells · doi:10.1002/stem.140269 · Cited by 66
Characterization of Mesenchymal Stem Cells Isolated from Mouse Fetal Bone Marrow
Wang, X., Hisha, H., Taketani, S., Adachi, Y., Li, Q., Cui, W., Cui, Y., Wang, J., Song, C., Mizokami, T., et al. (2005) · Stem Cells · doi:10.1634/stemcells.2005-0219 · Cited by 64
Effects of macrophage depletion on the induction of histidine decarboxylase by lipopolysaccharide, interleukin 1 and tumour necrosis factor
Endo, Y., Nakamura, M., Nitta, Y., & Kumagai, K. (1995) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1995.tb14924.x · Cited by 64
Fibroblast Growth Factor-1 and -2 Preserve Long-Term Repopulating Ability of Hematopoietic Stem Cells in Serum-Free Cultures
Yeoh, J. S. G., van Os, R. P., Weersing, E., Ausema, A., Dontje, B., Vellenga, E., & de Haan, G. (2006) · Stem Cells · doi:10.1634/stemcells.2005-0439 · Cited by 68
Modulated Expression of the Epidermal Growth Factor-Like Homeotic Protein dlk Influences Stromal-Cell–Pre-B-Cell Interactions, Stromal Cell Adipogenesis, and Pre-B-Cell Interleukin-7 Requirements
Bauer, S. R., Ruiz‐Hidalgo, M. J., Rudikoff, E. K., Goldstein, J., & Laborda, J. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.9.5247 · Cited by 63
Insulin-like growth factor-I enhances lymphoid and myeloid reconstitution after allogeneic bone marrow transplantation12
Alpdogan, N., Muriglan, S. J., Kappel, B. J., Doubrovina, E. S., Schmaltz, C., Schirò, R., Eng, J. M., Greenberg, A. S., Willis, L. M., Rotolo, J. A., et al. (2003) · Transplantation · doi:10.1097/01.tp.0000070167.81584.a2 · Cited by 63
Excessive production of transforming growth factor-beta by bone marrow stromal cells in B-cell chronic lymphocytic leukemia inhibits growth of hematopoietic precursors and interleukin-6 production
Lagneaux, L., Delforge, A., Dorval, C., Bron, D., & Stryckmans, P. (1993) · Blood · doi:10.1182/blood.v82.8.2379.2379 · Cited by 63
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Cheng, M., & Qin, G. (2012) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-398459-3.00011-3 · Cited by 66
Local signals in stem cell-based bone marrow regeneration
Han, W., Yan, Y., & Liu, X. (2006) · Cell Research · doi:10.1038/sj.cr.7310026 · Cited by 63
Bone Density Loss Is Associated With Blood Cell Counts
Valderrábano, R. J., Lui, L., Lee, J. S., Cummings, S. R., ORWOLL, E. S., Hoffman, A. R., & Wu, J. Y. (2016) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3000 · Cited by 61
Cell processing engineering for ex-vivo expansion of hematopoietic cells
Takagi, M. (2005) · Journal of Bioscience and Bioengineering · doi:10.1263/jbb.99.189 · Cited by 60
Chemokine expression by subchondral bone marrow stromal cells isolated from osteoarthritis (OA) and rheumatoid arthritis (RA) patients
Lisignoli, G., Toneguzzi, S., Pozzi, C., Piacentini, A., Grassi, F., Ferruzzi, A., Gualtieri, G., & FACCHINI, A. (1999) · Clinical & Experimental Immunology · doi:10.1046/j.1365-2249.1999.00893.x · Cited by 60
Hematopoietic stem-cell differentiation
Spangrude, G. J. (1991) · Current Opinion in Immunology · doi:10.1016/0952-7915(91)90046-4 · Cited by 60
In vitro reconstitution of human B-cell ontogeny: from CD34(+) multipotent progenitors to Ig-secreting cells.
Fluckiger, A.-C., Sanz, E., Garcia-Lloret, M., Su, T. T., Hao, Q., Kato, R. M., Quan, S. G., de la Hera, A., Crooks, G. M., Witte, O. N., et al. (1998) · PubMed · doi:10.1182/blood.v92.12.4509 · Cited by 60
B Lymphopoiesis in the Mouse
Rolink, A. G., & Melchers, F. (1993) · Advances in immunology · doi:10.1016/s0065-2776(08)60499-x · Cited by 60
Reconstitution of SCID mice with human lymphoid and myeloid cells after transplantation with human fetal bone marrow without the requirement for exogenous human cytokines.
Kollmann, T. R., Kim, A., Zhuang, X., Hachamovitch, M., & Goldstein, H. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.17.8032 · Cited by 60
Barrier cells in the spleen
WEISS, L. P. (1991) · Immunology Today · doi:10.1016/0167-5699(91)90108-6 · Cited by 58
Tachykinins in the emerging immune system: relevance to bone marrow homeostasis and maintenance of hematopoietic stem cells
Steven, J. G. (2004) · Frontiers in bioscience · doi:10.2741/1373 · Cited by 58
The critical role of agrin in the hematopoietic stem cell niche
Mazzon, C., Anselmo, A., Cibella, J., Soldani, C., Destro, A., Kim, N., Roncalli, M. G., Burden, S. J., Dustin, M. L., Sarukhan, A., et al. (2011) · Blood · doi:10.1182/blood-2011-01-331272 · Cited by 60
Hepatocyte growth factor plays roles in the induction and autocrine maintenance of bone marrow stromal cell IL-11, SDF-1α, and stem cell factor
Matsuda-Hashii, Y., Takai, K., Ohta, H., Fujisaki, H., Tokimasa, S., Osugi, Y., Ozono, K., Matsumoto, K., Nakamura, T., & Hara, J. (2004) · Experimental Hematology · doi:10.1016/j.exphem.2004.06.012 · Cited by 57
Genome‐wide expression reveals multiple systemic effects associated with detection of anticoagulant poisons in bobcats (Lynx rufus)
Fraser, D. L., Mouton, A., Serieys, L. E. K., Cole, S. W., Carver, S., VandeWoude, S., Lappin, M. R., Riley, S. P. D., & Wayne, R. K. (2018) · Molecular Ecology · doi:10.1111/mec.14531 · Cited by 58
Hematopoietic supportive functions of mouse bone marrow and fetal liver microenvironment: dissection of granulocyte, B-lymphocyte, and hematopoietic progenitor support at the stroma cell clone level
Friedrich, C., Zausch, E., Sugrue, S. P., & Gutierrez-Ramos, J.-C. (1996) · Blood · doi:10.1182/blood.v87.11.4596.bloodjournal87114596 · Cited by 54
A Novel Spliced Form of SH2-Containing Inositol Phosphatase Is Expressed During Myeloid Development
Lucas, D. M., & Rohrschneider, L. R. (1999) · Blood · doi:10.1182/blood.v93.6.1922.406k21_1922_1933 · Cited by 54
Immune Tolerance vs. Immune Resistance: The Interaction Between Host and Pathogens in Infectious Diseases
Ahmad, H. I., Jabbar, A., Mushtaq, N., Javed, Z., Hayyat, M. U., Bashir, J., Naseeb, I., Abideen, Z. U., Ahmad, N., & Chen, J. (2022) · Frontiers in Veterinary Science · doi:10.3389/fvets.2022.827407 · Cited by 61
Induction of apoptosis in bone marrow neutrophil-lineage cells by classical swine fever virus
Summerfield, A., Zingle, K., Inumaru, S., & McCullough, K. C. (2001) · Journal of General Virology · doi:10.1099/0022-1317-82-6-1309 · Cited by 53
Stromal Cell CD9 Regulates Differentiation of Hematopoietic Stem/Progenitor Cells
Aoyama, K., Oritani, K., Yokota, T., Ishikawa, J., Nishiura, T., Miyake, K., Kanakura, Y., Tomiyama, Y., Kincade, P. W., & Matsuzawa, Y. (1999) · Blood · doi:10.1182/blood.v93.8.2586 · Cited by 53
Differentiation of canine bone marrow cells with hemopoietic characteristics from an adherent stromal cell precursor.
Huss, R., Hong, D.-S., McSweeney, P. A., Hoy, C. A., & Deeg, H. J. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.3.748 · Cited by 53
CD14+ cells in granulocyte colony-stimulating factor (G-CSF)-mobilized peripheral blood mononuclear cells induce secretion of interleukin-6 and G-CSF by marrow stroma
Mielcarek, M. B., Roecklein, B. A., & Torok-Storb, B. (1996) · Blood · doi:10.1182/blood.v87.2.574.bloodjournal872574 · Cited by 53
The stromal composition of malignant lymphoid aggregates in bone marrow: variations in architecture and phenotype in different B‐cell tumours
Vega, F., Medeiros, L. J., Lang, W., Mansoor, A., Bueso-Ramos, C., & Jones, D. (2002) · British Journal of Haematology · doi:10.1046/j.1365-2141.2002.03497.x · Cited by 52
Lymphodepletion in the ApcMin/+ mouse model of intestinal tumorigenesis
Coletta, P. L., Müller, A. M., Jones, E., Mühl, B., Holwell, S. E., Clarke, D., Meade, J. L., Cook, G. P., Hawcroft, G., Ponchel, F., et al. (2003) · Blood · doi:10.1182/blood-2003-03-0707 · Cited by 53
Inhibition of hepatic stellate cells by bone marrow-derived mesenchymal stem cells in hepatic fibrosis
Jang, Y. O., Jun, B. G., Baik, S. K., Kim, M. Y., & Kwon, S. O. (2015) · Clinical and Molecular Hepatology · doi:10.3350/cmh.2015.21.2.141 · Cited by 52
Regulation of hematopoiesis by gap junction-mediated intercellular communication
Montecino‐Rodriguez, E., & Dorshkind, K. A. (2001) · Journal of Leukocyte Biology · doi:10.1189/jlb.70.3.341 · Cited by 52
Expression of activin A/erythroid differentiation factor in murine bone marrow stromal cells
Yamashita, T., Takahashi, S., & Ogata, E. (1992) · Blood · doi:10.1182/blood.v79.2.304.304 · Cited by 52
Clozapine bioactivation induces dose-dependent, drug-specific toxicity of human bone marrow stromal cells: A potential in vitro system for the study of agranulocytosis
Pereira, A. M., & Dean, B. (2006) · Biochemical Pharmacology · doi:10.1016/j.bcp.2006.06.006 · Cited by 51
Hematopoietic Reconstitution of Syngeneic Mice with a Peripheral Blood-Derived, Monoclonal CD34-, Sca-1+, Thy-1low, c-kit+ Stem Cell Line
Lange, C., Kaltz, C., Thalmeier, K., Hans-Jochem, & Huss, R. (1999) · Stem Cells and Development · doi:10.1089/152581699320090 · Cited by 51
TRANSPLANTATION OF ALLOGENEIC OR XENOGENEIC BONE MARROW WITHIN THE DONOR STROMAL MICROENVIRONMENT1
Gurevitch, O. A., Prigozhina, T. B., Pugatsch, T., & Slavin, S. (1999) · Transplantation · doi:10.1097/00007890-199911150-00024 · Cited by 51
Mitogenic and adhesive effects of tenascin-C on human hematopoietic cells are mediated by various functional domains
Seiffert, M., Beck, S. C., Schermutzki, F., Müller, C. A., Erickson, H., & Klein, G. (1998) · Matrix Biology · doi:10.1016/s0945-053x(98)90124-x · Cited by 50
Bone Marrow Stroma-Derived Prolactin Is Involved in Basal and Platelet-Activating Factor–Stimulated In Vitro Erythropoiesis
Bellone, G., Astarita, P., Artusio, E., Silvestri, S., Mareschi, K., Turletti, A., Buttiglieri, S., Emanuelli, G., & Matera, L. (1997) · Blood · doi:10.1182/blood.v90.1.21 · Cited by 50
Drugs toxic to the bone marrow that target the stromal cells
Guest, I., & Uetrecht, J. (2000) · Immunopharmacology · doi:10.1016/s0162-3109(99)00168-x · Cited by 49
The bone marrow niche in support of breast cancer dormancy
Walker, N. D., Patel, J. S., Munoz, J. L., Hu, M. D., Guiro, K., Sinha, G., & Rameshwar, P. (2015) · Cancer Letters · doi:10.1016/j.canlet.2015.10.033 · Cited by 47
Bone Marrow-Derived Macrophages Express Functional CGRP Receptors and Respond to CGRP by Increasing Transcription of c-fos and IL-6 mRNA
Fernandez, S., Knopf, M. A., Bjork, S. K., & McGillis, J. P. (2001) · Cellular Immunology · doi:10.1006/cimm.2001.1795 · Cited by 47
Low-intensity pulsed ultrasound (LIPUS) and cell-to-cell communication in bone marrow stromal cells
Sena, K., Angle, S. R., Kanaji, A., Aher, C. V., Karwo, D., Sumner, D. R., & Virdi, A. S. (2011) · Ultrasonics · doi:10.1016/j.ultras.2011.01.007 · Cited by 47
IL-6 AND IL-8 PRODUCTION BY HUMAN BONE MARROW STROMAL CELLS
Rougier, F., Cornu, É., Praloran, V., & Denizot, Y. (1998) · Cytokine · doi:10.1006/cyto.1997.0262 · Cited by 47
Definition of a Novel Cellular Constituent of the Bone Marrow That Regulates the Response of Immature B Cells to B Cell Antigen Receptor Engagement
Sandel, P. C., Gendelman, M., Kelsoe, G. H., & Monroe, J. G. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.10.5935 · Cited by 46
Ig DH Gene Segment Transcription and Rearrangement Before Surface Expression of the Pan-B–Cell Marker CD19 in Normal Human Bone Marrow
Bertrand, F. E., Billips, L. G., Burrows, P. D., Gartland, G. L., Kubagawa, H., & Schroeder, H. W. (1997) · Blood · doi:10.1182/blood.v90.2.736 · Cited by 46
Stromal Cell-Independent Maturation of IL-7-Responsive Pro-B Cells
Ray, R. J., Stoddart, A., Pennycook, J. L. M. H., Huner, H. O., Furlonger, C. L., Wu, G. E., & Paige, C. J. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.160.12.5886 · Cited by 46
GATA transcription in a small rhodamine 123lowCD34+ subpopulation of a peripheral blood–derived CD34−CD105+ mesenchymal cell line
Conrad, C. H., Göttgens, B., Kinston, S., Ellwart, J. W., & Huss, R. (2002) · Experimental Hematology · doi:10.1016/s0301-472x(02)00865-2 · Cited by 45
IL-5 production by bone marrow stromal cells: Implications for eosinophilia associated with asthma
Hogan, M. B., Piktel, D., & Landreth, K. S. (2000) · Journal of Allergy and Clinical Immunology · doi:10.1067/mai.2000.108309 · Cited by 45
Osteogenic growth peptide increases blood and bone marrow cellularity and enhances engraftment of bone marrow transplants in mice
Gurevitch, O. A., Slavin, S., Mühlrád, A., Shteyer, A., Gazit, D., Chorev, M., Vidson, M., Attar-Namdar, M., Berger, É., Bleiberg, I., et al. (1996) · Blood · doi:10.1182/blood.v88.12.4719.bloodjournal88124719 · Cited by 45
Nerve growth factor is involved in the supportive effect by bone marrow- -derived stromal cells of the factor-dependent human cell line UT-7 [published erratum appears in Blood 1996 Oct 1;88(7):2818]
Auffray, I., Chevalier, S., Froger, J., Izac, B., Vainchenker, W., Gascan, H., & Coulombel, L. (1996) · Blood · doi:10.1182/blood.v88.5.1608.1608 · Cited by 45
Mesenchymal Stem Cell Therapy for Protection and Repair of Injured Vital Organs
van Poll, D., Parekkadan, B., Rinkes, I. H. M. B., Tilles, A. W., & Yarmush, M. L. (2008) · Cellular and Molecular Bioengineering · doi:10.1007/s12195-008-0001-2 · Cited by 48
Intercellular communication between bone marrow stromal cells and CD34+ haematopoietic progenitor cells is mediated by connexin 43-type gap junctions
Dürig, J., Rosenthal, C., Halfmeyer, K., Wiemann, M., Novotný, J., Bingmann, D., Dührsen, U., & Schirrmacher, K. (2000) · British Journal of Haematology · doi:10.1046/j.1365-2141.2000.02385.x · Cited by 44
CXCR4 in Clinical Hematology
Calandra, G. C., Bridger, G. J., & Fricker, S. P. (2010) · Current topics in microbiology and immunology · doi:10.1007/82_2010_26 · Cited by 43
Stromal cells modulate TCL1 expression, interacting AP-1 components and TCL1-targeting micro-RNAs in chronic lymphocytic leukemia
Sivina, M., Hartmann, E., Vasyutina, E. L., Bouças, J., Breuer, A., Keating, M. J., Wierda, W. G., Rosenwald, A., Herling, M., & Burger, J. A. (2012) · Leukemia · doi:10.1038/leu.2012.63 · Cited by 42
Expression of Stromal Cell-Derived Factor-1/Pre-B Cell Growth-Stimulating Factor Receptor, CXC Chemokine Receptor 4, on CD34+ Human Bone Marrow Cells Is a Phenotypic Alteration for Committed Lymphoid Progenitors
Ishii, T., Nishihara, M., Ma, F., Ebihara, Y., Tsuji, K., Asano, S., Nakahata, T., & Maekawa, T. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.163.7.3612 · Cited by 42
In-vitro analyses of mechanisms of B-cell development
Rolink, A. G., Ghia, P., Grawunder, U., Haasner, D., Karasuyama, H., Kalberer, C. P., Winkler, T., & Melchers, F. (1995) · Seminars in Immunology · doi:10.1016/1044-5323(95)90043-8 · Cited by 42
Direct contact between CD34+lin− cells and stroma induces a soluble activity that specifically increases primitive hematopoietic cell production
Koller, M. R., Oxender, M., Jensen, T. C., Goltry, K. L., & Smith, A. K. (1999) · Experimental Hematology · doi:10.1016/s0301-472x(98)00080-0 · Cited by 42
Mesenchymal Stem Cells Enhance the Induction of Mixed Chimerism and Tolerance to Rat Hind-Limb Allografts after Bone Marrow Transplantation
Pan, H., Zhao, K., Wang, L., Yan, Z., Zhang, G., Mai, H.-X., Han, Y., Li, Y., & Guo, S. (2008) · Journal of Surgical Research · doi:10.1016/j.jss.2008.09.027 · Cited by 41
Leptin receptor/CD295 is upregulated on primary human mesenchymal stem cells of advancing biological age and distinctly marks the subpopulation of dying cells
Laschober, G. T., Brunauer, R., Jamnig, A., Fehrer, C., Greiderer‐Kleinlercher, B., & Lepperdinger, G. (2008) · Experimental Gerontology · doi:10.1016/j.exger.2008.05.013 · Cited by 41
Cytokine production and heterogeneity of primary stromal cells that support B lymphopoiesis
Witte, P. L., Frantsve, L. M. E., Hergott, M., & Rahbe, S. M. (1993) · European Journal of Immunology · doi:10.1002/eji.1830230812 · Cited by 41
Regulated Expression of the Eph-Related Receptor Tyrosine Kinase Hek11 in Early Human B Lymphopoiesis
Aasheim, H., Terstappen, L. W. M. M., & Logtenberg, T. (1997) · Blood · doi:10.1182/blood.v90.9.3613 · Cited by 41

Authors: Dorshkind, K.
Affiliations: University of California, Riverside (US)
Corresponding author: Dorshkind, Kenneth
ORCID: Dorshkind, Kenneth
Venue: Annual Review of Immunology
Publisher: Annual Reviews
Published: 1990-04
Volume: 8
Issue: 1
Pages: 111-137
ISSN: 0732-0582 (ISSN-L)
1545-3278
DOI: 10.1146/annurev.iy.08.040190.000551
OpenAlex: W2177231732
Cited by: 504
References: 100
Citations by year: 2025: 2 · 2024: 1 · 2023: 2 · 2022: 7 · 2020: 3 · 2019: 3 · 2018: 3 · 2017: 3 · 2016: 4 · 2015: 9 · 2014: 4 · 2013: 9 · 2012: 10
FWCI: 14.48
Type: journal article
Language: en
Open access: closed
Locations: Annual Review of Immunology (publishedVersion)
PubMed (publishedVersion)
Funders: National Institutes of Health (5r01hl036591-08)
U.S. Public Health Service (A100843)
National Heart, Lung, and Blood Institute (HL-36591)
National Institute of Allergy and Infectious Diseases (AI21256)
Topics: Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
Keywords: hematopoiesis, mesenchymal stem cells, bone marrow microenvironment, hematopoietic stem cells, stromal cell-derived factor
MeSH terms: Animals, Bone Marrow, Bone Marrow Cells, Cell Communication, Colony-Stimulating Factors, Extracellular Matrix, Hematopoiesis, Humans

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Regulation of Hemopoiesis by Bone Marrow Stromal Cells and Their Products

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