Calf thymus polypeptide improved hematopoiesis via regulating colony-stimulating factors in BALB/c mice with hematopoietic dysfunction

Int J Biol Macromol. 2020 Aug 1:156:204-216. doi: 10.1016/j.ijbiomac.2020.03.041. Epub 2020 Mar 7.

Abstract

Calf thymus polypeptide (CTP) is prepared from calf thymus. It has a molecular mass of <10 kilodalton (kDa) and contains 17 types of amino acids. This study investigated the hematopoietic function-improvement effect of CTP in CHRF, K562, and bone marrow mononuclear cells; mice with immunosuppression; and with hematopoietic dysfunction. In mice with immunosuppression, CTP enhanced the cytotoxic activity of natural killer cells and the proliferation of lymphocytes and regulated the levels of immunoglobulins. It also enhanced the proliferation and differentiation of CHRF and K562 cells by upregulating the expression of proliferation- and differentiation-related proteins. In mice with hematopoietic dysfunction, CTP restored white blood cell, neutrophil, and hemoglobin proportions in the peripheral blood and enhanced the levels of B lymphocytes and hematopoietic stem cells and progenitor cells in the bone marrow. CTP effectively regulated the levels of hematopoiesis-related cytokines, such as granulocyte colony-stimulating factor (G-CSF), macrophage colony-stimulating factor (M-CSF), interleukin 2, and interferons-γ, and enhanced the expression of hematopoiesis-related proteins in both primary bone marrow cells and mice with hematopoietic dysfunction. These results indicate that CTP has hematopoietic function-improvement effect and this effect may be related to the modulation of colony-stimulating factors (CSFs) and related signaling pathways.

Keywords: Calf thymus polypeptide; Colony-stimulating factors; Hematopoiesis; Hematopoietic dysfunction; Hematopoietic stem cells.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Biomarkers
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / metabolism
  • Cattle
  • Cell Cycle / drug effects
  • Cell Differentiation / drug effects
  • Cell Line
  • Colony-Stimulating Factors / genetics*
  • Colony-Stimulating Factors / metabolism
  • Cytokines / metabolism
  • Gene Expression Regulation / drug effects*
  • Hematopoiesis / drug effects*
  • Hematopoiesis / genetics*
  • Hematopoietic Stem Cells / cytology
  • Hematopoietic Stem Cells / drug effects
  • Hematopoietic Stem Cells / metabolism
  • Humans
  • Immunocompromised Host
  • Immunologic Factors / chemistry
  • Immunologic Factors / pharmacology
  • Immunomodulation / drug effects
  • Immunophenotyping
  • Lymphocyte Activation
  • Lymphocytes / drug effects
  • Lymphocytes / immunology
  • Lymphocytes / metabolism
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Molecular Weight
  • Organ Specificity / immunology
  • Peptides / chemistry
  • Peptides / pharmacology*
  • Thymus Gland / metabolism

Substances

  • Biomarkers
  • Colony-Stimulating Factors
  • Cytokines
  • Immunologic Factors
  • Peptides