2008, Número 1
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Rev Invest Clin 2008; 60 (1)
BMP4: Importante regulador del desarrollo embrionario y la hematopoyesis
Fernández-Sánchez V, Mayani H
Idioma: Español
Referencias bibliográficas: 39
Paginas: 68-74
Archivo PDF: 66.30 Kb.
RESUMEN
Las proteínas morfogénicas del hueso (BMPs) son factores de
crecimiento multifuncionales, que pertenecen a la superfamilia
del factor de crecimiento transformante-β (TGF-β). El papel
de las BMPs en el desarrollo embrionario, así como sus
funciones celulares en la etapa postnatal, han sido extensamente
estudiadas en años recientes. Una de dichas proteínas
es BMP4, la cual ha sido identificada como un regulador
pleiotrópico, fundamental para la formación del mesodermo y
para la especificación vascular/hematopoyética durante el desarrollo.
El estudio de las moléculas que regulan la proliferación,
expansión y diferenciación de las células troncales
hematopoyéticas (CTH) y células progenitoras hematopoyéticas
(CPH) se han enfocado al estudio de algunas citocinas hematopoyéticas,
sin embargo, estudios recientes han sugerido
que BMP4, al igual que otras moléculas que actúan como
morfógenos en la etapa embrionaria, juegan un papel importante
en la especificaciones de la hematopoyesis del adulto. En
este trabajo se pretende destacar la importancia de BMP4 durante
el desarrollo embrionario y su papel en la expansión de
CTH y CPH, particularmente aquellas provenientes de la sangre
de cordón umbilical (SCU).
REFERENCIAS (EN ESTE ARTÍCULO)
Jones JM, Thomson JA. Human embryonic stem cells technology. Semin Reprod Med 2000; 18: 219-23.
Scot F.G. Development biology. 7a Ed. Sinauer Associates; Inc. (capitulo 6,7), 2003.
Ilancheran S, Michalska A, Peh G, Wallece EM, Pera M, Manuelpillai U. Stem Cells Derived from Human Fetal Membranes Display Multi-Lineage Differentiation Potential. Biol Reprod 2007; 77(3): 577-88
Bhardwaj G, Murdoch B, Wu D, et al. Sonic hedgehog induces the proliferation of primitive human hematopoietic cells via BMP regulation. Nature immunology 2001; 2(2): 172-9.
Baron MH. Induction of embryonic hematopoietic and endothelial stem/progenitor cells by hedgehog-mediated signals. Differentiation 2001; 68: 175-85.
Behringer RR. Developmental biology. Dance of the embryo. Science 2007; 316(5825): 697-8.
Kenji S, Hata A. Indian Hedgehog gene is a target of the bone morphogenetic protein signaling pathway. J Biol Chem 2004; 279(18): 18544-9.
Chen Di, Zhao M, Mundy GR. Bone Morphogenetic proteins. Growth Factor. 2004; 22(4): 233-41.
Hutton JF, Rozenkov V, Khor FSL, D´Andrea JD, Lewis ID. Bone Morphogenetic Protein 4 Contributes to the Maintenance of Primitive Cord Blood Hematopoietic Progenitors in an Ex Vivo Stroma-Noncontact Co-Culture System. Stem Cells and Development 2006; 15: 805-13.
Bandyopadhyay A, Tsuji K, Harfe BD, Rosen V, Tabin CJ. Genetic analysis of the roles of BMP2, BMP4 and BMP7 in limb patternig and skeletogenesis. Plos Genet 2006; 2(12): 2116-30.
Detmer K. y Walker A.N. Bone morphogenetic proteins act synergistically with haematopoietic cytokines in the differentiation of haematopoietic progenitors. Citokine 2002; 17(1): 36-47.
Wozney JM, Rosen V, Celeste AJ, Mitsock LM, et al. Novel regulators of bone formation molecular clones and activities. Science 1988; 242: 1528-33.
Wijngaard VA, Kraay VM, Zoelen VEJ, Olijve W, Boersma CJC. Genomic Organization of the human bone morphogenetic protein- 4 gene: molecular basis of multiple transcripts. Biochemical and Biophysical Research Communications 1996; 219: 789-94.
Bathia M, Bonnet D, Wu D, et al. Bone Morphogenetic Proteins Regulate the Developmental program of human hematopoietic stem cells. J Exp Med 1999; 189(7): 1139-47.
Singbrant S, Moody LJ, Blank U, Karlosson G, Umans L, Zwijsen S, et al. Smad 5 is dispensable for adult murine hematopoiesis. Blood 2006; 108(12): 3707-12.
Karlsson G, Blank U, Moody Jl, Ehinger M, Singbrant S, Dent CX, et al. Smand 4 is critical for sel-renawal of hematopoietic stem cells. J Exp Med 2007; 204(3): 467-74.
Dahlqvist C, Blokzijl A, Chapmna G, Falk A, Dannaeus K, Ibañez FC, et al. Funtional Notch signaling is required for BMP-4 induced inhibition of myogenic differentiation. Development 2003; 130: 6089-99.
Bitgood M, Mc Mahon A. Hedgehog and BMP genes are coexpressed at many diverse sites of cell-cell interaction in the mouse embryo. Dev Biol 1995; 172: 126-38.
Wozney JM. The bone morphogenetic protein family and osteogenesis. Mol Reprod Dev 1992; 32(2): 160-7.
Zon LI. Self-renewal versus differentiation, a job for the mighty morphogens. Nature Immunology 2001; 2(2): 142-3.
Sadlon TJ, Lewis ID, D’Andrea Richard J. BMP4: its role in development of the hematopoietic system potencial as a hematopoietic growth factor. Stem Cells 2004; 22: 457-74.
Chen J, Leong SY, Schachner M. Differential expression of cell fate determinants in neurons and glial cells of adult mouse spinal cord after compression injury. Eur J Neurosci 2005; 22(8): 1895-906.
Enzmann GU, Benton RL, Woock JP, Howard RM, Tsoulfas P y Whittemore SR. Consequences of noggin expression by neural stem, glial, and neuronal precursor cells engrafted into the injured spinal cord. Exp Neurol 2005; 195(2): 293-304.
Ferraris EZ. Histología y embriología bucodental. Ed. Panamericana. 1999; 1: 80-1.
Limura OS, Maruoka Y, Takeda K, Sasaki S. Cloning and sequence of bone morphogenetic protein 4 (BMP-4) from a human placental cDNA library. DNA Seq 1995; 5(5): 273-5.
Jeffery T, Upton DP, Trembath CR and Morrell W. BMP4 inhits proliferation and promotes myocyte differentiation of lung fibroblasts via Smad 1 and JNK pathways. Am J Physiol Lung Cell Mol Physiol 2005; 288: L370-L378.
Li H, Corrales CE, Wang Z, Zhao Y, Wang Y, Heller S. BMP4 signaling is involved in the generation of inner ear sensory epithelial. BMC Dev Biol 2005; 17(5): 16.
Pujades C, Kamaid A, Alsina B, Giraldez F. BMP-signaling regulates the generation of hair-cells. Dev Biol 2006; 292(1): 55-67.
Johansson BM, Wiles MV. Evidence for involvement of activin A and bone morphogenetic protein 4 in mesoderm and hematopoietic development. Mol Cell Biol 1995; 15(1): 141-51.
Dzierzak E, Medvinsky A, Merella de B. Qualitative and quantitative aspects of hematopoietic cell development in the mammalian embryo. Immunology Today 1998; 5: 228-35.
Park C, Afrikanova I, Chung YS, Zhang WJ, et al. A hierarchical order of factors in the generation of FLK-1 and SCL- expressing hematopoietic and endothelial progenitors from embryonic stem cells. Dev Disease 2004; 131: 2749-62.
Boyd NL, Dhara SK, Rekaya R, Godbey EA, Hasneen K, Rao RR, et al. BMP4 Promotes Formation of Primitive Vascular Networks in Human Embryonic Stem Cell-Derived Embryoid Bodies. Exp Biol Med 2007; 232(6): 833-43.
Mayani H, Lansdorp PM. Biology of human umbilical cord blood-derived hematopoyetic stem/progenitor cells. Stem Cells 1998; 16: 153-65.
Flores-Guzman P, Gutierrez RM, Mayani H. In vitro proliferation, expantion and diferentiation of a CD34+ cell-enriched hematopoietic cell population from human umbilical cord blood in response to recombinant cytokines. Archives of Medical Research 2002; 33: 107-14.
Flores-Guzman P, Flores FE, Martinez JG, Mayani H. In vitro characterization of two lineage-negative CD34+ cell-enriched hematopoietic cell populations from human UC blood. Cytotherapy 2005; 7(4): 334-44.
Scheller M, Huelsken J, Rosenbauer F. Taketo MM, Birchmeier W, Tenen DG, et al. Hematopoietic stem cells and multilineage defects generated by constitutive β-catenin activation. Nature Immunology 2006; 7(10): 1037-45.
Karanu FN, Murdoch B, Gallacher L, Wu DM, Koremoto M, Bhatia M. The notch ligand jagged-1 represent a novel growth factor of human hematopoietic stem cells. J Exp Med 2000; 192(9): 1365-72.
Pick M, Azzola L, Mossman A, Stanley EG, Elefanty AG. Differentiation of Human Embryonic Stem Cells in Serum Free Medium Reveals Distinct Roles for BMP4, VEGF, SCF and FGF2 in Hematopoiesis. Stem Cells 2007; 25(9): 2206-14.
Chadwick K, Wang LL, Menendez P, Murdoch B, Rouleau A, Bhatia M. Cytokines and BMP4 promote hematopoietic differentiation of embryonic stem cells. Blood 2003; 102(3): 906-15.