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Lectin-derived progenitor cell preservation factors and methods of useRelated Patent Categories: Drug, Bio-affecting And Body Treating Compositions, Lymphokine, InterleukinLectin-derived progenitor cell preservation factors and methods of use description/claimsThe Patent Description & Claims data below is from USPTO Patent Application 20070280904, Lectin-derived progenitor cell preservation factors and methods of use. Brief Patent Description - Full Patent Description - Patent Application Claims
BACKGROUND OF THE INVENTION [0001] The invention relates to a nucleic acid and its corresponding protein for use in connection with the preservation of progenitor cells. More specifically, the invention relates to a nucleic acid and the protein that it encodes and which is capable of preserving progenitor cells, as well as a method of using the protein for preserving progenitor cells. [0002] Each day the bone marrow generates and releases into the circulation several billion fully-differentiated, functional blood cells. Production of these cells derives from a small stock of quiescent progenitor cells (including the most primitive stem cells and other less primitive but still immature progenitors) by a process called hematopoiesis (Zipori 1992). The most primitive stem cells have the capacity to generate >10.sup.13 cells containing all blood lineages (Turhan et al. 1989). The production of such a large number of cells is achieved by extensive proliferation coupled with successive differentiation steps leading to a balanced production of mature cells. Progenitor cells progressively lose their capacity to generate multiple cells lineages and eventually produce cells of one or two cell lineages. [0003] Soluble regulators and cell-cell interactions mediate differentiation pathways of immature progenitors through a tightly-controlled but inadequately understood process. Several of the body's soluble factors have been isolated and characterized both in culture and in animals (see, e.g., Ogawa (1993) and references therein). Regulators such as the colony stimulating factors (e.g., IL3, GM-CSF, G-CSF, M-CSF) not only induce proliferation and differentiation of progenitors capable of producing cells of either multiple cell lineages (IL3 and GM-CSF) or single cell lineages (G-CSF and M-CSF), but also preserve viability of their respective progenitors for short periods. Other regulators such as interleukin-1 (IL1), the kit ligand (KL), and thrombopoietin (Borge et al. 1996) increase viability of multipotential progenitors in addition to other functions. No known cytokines alone or in combination can preserve viability of primitive progenitors in liquid culture without stromal support beyond a few days. [0004] Regulation of primitive stem cells appears to differ from that of immature, multilineage progenitors. Hematopoietic stem cells, which reside in the bone marrow predominantly in a quiescent state, do not appear to respond immediately to regulators that induce differentiation and proliferation. Maintenance of these cells in the body is mediated via cell-cell interactions and soluble regulators. Maintenance of quiescent stem cells in vitro has been achieved by culturing cells on adherent stromal layers with soluble regulators such as IL3, IL6, KL and LIF (Young et al. 1996). Recently, the addition of the FLK2/FLT3 ligand (FL) to this complex culture has been found to extend maintenance of quiescent stem cells from a few weeks to three months (Shah et al. 1996). [0005] While the use of stromal cell culture has heretofore proven to be useful for the maintenance of hematopoietic stems cells in the laboratory setting, such approaches are not easily amenable to clinical application. Isolating and establishing stromal cell cultures for individual patients is not practical either because of time constraints or because a patient's marrow may be compromised by the underlying disease or exposure to agents (e.g., radiation, chemotherapy) that can damage the bone marrow microenvironment. [0006] Lectins, defined as carbohydrate-binding proteins other than antibodies or enzymes, (Baronedes 1988), are widespread among plants, prokaryotes, and eukaryotes (see generally, Gabius et al. 1993). Each lectin recognizes a specific carbohydrate moiety, and forms a non-covalent bond with the carbohydrate through a stereochemical fit of complementary domains (e.g., hydrophobic pocket). Carbohydrates are widely present on cell surfaces (in the forms of glycoproteins, glycolipids, and polysaccharides), and appear to mediate cell-cell contacts including cell recognition (Sharon et al. 1989). Abnormal glycosylation patterns are associated with disease by causing alterations in a protein's surface properties, conformation, stability, or protease resistance (Dwek 1995). [0007] Gowda et al. (1994) described the isolation of a mannose-glucose-specific lectin from the hyacinth bean (Dolichos lab lab). Purification and sequencing of this lectin is said to indicate that the protein includes two nonidentical subunits. The Gowda et al. publication describes evolutionary relationships of the lectin to other lectins, but does not ascribe any function to the protein beyond saccharide-binding. [0008] Cell agglutinating properties of certain plant lectins have been known for over 100 years. Certain lectins have been used as tools in immunology laboratories as potent, specific activators of T lymphocytes (phytohemagglutinin (PHA) and concanavalin A (ConA)) and B lymphocytes (pokeweed mitogen (PWM)) for over 30 years (Sharon et al. 1989). Some lectins have also been used to isolate hematopoietic progenitors for over 15 years (Gabius 1994a). Large numbers of cancer patients in Europe have received crude extracts of mistletoe lectin (Viscum album) intravenously as a candidate cancer therapy without major complications (Gabius 1994b). Whether these plant lectins act on mammalian cells via de novo means, or simply mimic their functional mammalian homologs is not yet known. No lectin has yet been successfully developed as a human therapeutic. [0009] In view of the above considerations, it is clear that regulation of the hematopoietic process remains incompletely understood. Most soluble regulators identified, such as the colony stimulating factors and interleukins, induce proliferation and differentiation of progenitors cells in culture and their levels in the blood circulation increase during times of hematopoietic stress (e.g., blood loss, infection). For example, U.S. Pat. No. 4,808,611 describes a method of using IL1 and a colony stimulating factor to induce proliferation and differentiation of hemopoietic stem cells. Some soluble regulators, such as IL1, IL6, IL11, KL, FL, and Tpo, marginally increase viability of primitive progenitors on their own, but when added in combination induce proliferation and differentiation of progenitors. Soluble regulators that maintain or expand primitive progenitors for extended periods in the absence of stromal support are not yet commercially available. As a consequence, numerous potential therapeutic approaches to diseases such as cancer and genetic blood diseases remain unexplored. [0010] Accordingly, it is one of the purposes of this invention to overcome the above limitations in methods of regulating hematopoietic processes, by providing a factor and method of protecting, preserving, and expanding hematopoietic progenitor cell populations. It is another purpose of the invention to provide means for protecting the integrity of the hematopoietic processes in vivo as an adjunct to therapeutic treatments related to cancer and other diseases that can otherwise adversely impact upon the hematopoietic system. SUMMARY OF THE INVENTION [0011] It has now been discovered that these and other objectives can be achieved by the present invention, which provides an isolated nucleic acid comprising a nucleotide sequence as defined by SEQ ID NO:1, a homolog thereof, or a unique fragment thereof that encodes an amino acid sequence TNNVLQVT. [0012] The isolated nucleic acid preferably encodes a mannose/glucose-specific legume lectin, and is more preferably isolated from a legume of the tribe Phaseoleae. Most preferably, the protein is encoded by a nucleic acid that is isolated from red kidney beans, white kidney beans, hyacinth beans, or black-eyed peas. The isolated nucleic acid of the invention preferably comprises a nucleotide sequence as defined by SEQ ID NO:1 or a unique fragment thereof. [0013] Also, the protein encoded by the nucleic acid of the invention is capable of preserving progenitor cells that are at least unipotent progenitor cells, but the protein can be used to preserve pluripotent progenitor cells, as well as totipotent progenitor cells. In a preferred case, the protein can preserve hematopoietic progenitor cells, but progenitor cells from other tissues can also be preserved, including nerve, muscle, skin, gut, bone, kidney, liver, pancreas, or thymus progenitor cells. The progenitor cells capable of preservation according to the invention may express the CD34 antigen. More preferably, the progenitor cells express both CD34 and the FLK2/FLT3 receptor. Still more preferably, the progenitor cells express the FLK2/FLT3 receptor but do not express CD34. The protein can also be used to preserve cells that have been modified to express FLK2/FLT3 receptors on their surface. Thus, the invention provides a protein that has significant binding affinity for FLK2/FLT3 receptor on the cells, wherein binding of the protein with the FLK2/FLT3 receptor mediates the inhibition of differentiation of the cells. [0014] The invention further provides a method for preserving progenitor cells, comprising contacting progenitor cells with a protein encoded by an isolated nucleic acid comprising a nucleotide sequence defined by SEQ ID NO:1, a homolog thereof, or a fragment thereof that encodes an amino acid sequence TNNVLQVT, in an amount sufficient to preserve the progenitor cells. [0015] The method of the invention is useful for preserving progenitor cells from other species, particularly mammalian species. The progenitor cells preferably comprise cells of hematopoietic origin. The method can be used for preserving any human progenitor cells that express the CD34 antigen and/or the FLK2/FLT3 receptor. Alternatively, the method can be used to preserve any murine progenitor cells that express the Sca antigen, but that do not express mature blood cell lineage antigens. [0016] The method can comprise contacting the progenitor cells with the protein in vitro, ex vivo, or in vivo. In addition, the method can further comprise contacting the progenitor cells with FLK2/FLT3 ligand in an amount sufficient to selectively expand the number of progenitor cells without inducing differentiation thereof. [0017] In another embodiment, the invention is a method of treating a mammal in need of hematopoietic therapy, comprising: [0018] a) obtaining a tissue sample from the mammal, the tissue sample comprising hematopoietic progenitor cells; [0019] b) culturing the progenitor cells in the presence of a protein that preserves the progenitor cells, to provide cultured cells enriched in the progenitor cells, wherein the protein is encoded by an isolated nucleic acid comprising a nucleotide sequence defined by SEQ ID NO:1, a homolog thereof, or a fragment thereof that encodes an amino acid sequence TNNVLQVT; [0020] c) subjecting the mammal to conditions sufficient to effect myeloablation; and [0021] d) administering the cultured cells to the mammal following the myeloablation to reconstitute the hematopoietic system of the mammal. [0022] According to the method, the myeloablation conditions can comprise bone marrow irradiation, whole body irradiation, or chemically-induced myeloablation. 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