Establishment of an ATLL cell line (YG-PLL) dependent on IL-2 and IL-4, which are replaced by OX40-ligand+ HK with poly-L-histidine and dermatan sulfate

J Clin Exp Hematop. 2021 Sep 10;61(3):145-151. doi: 10.3960/jslrt.20058. Epub 2021 Jul 31.

Abstract

We established an IL-2 and IL-4 (IL2/4) - dependent adult T-cell leukemia/lymphoma (ATLL) cell line (YG-PLL) by adding poly-L-lysine (PLL) to the culture medium. YG-PLL originates from lymphoma cells and contains a defective HTLV-I proviral genome. Although YG-PLL cannot survive without IL-2/4, the follicular dendritic cell (FDC)-like cell line HK expressing OX40-ligand gene (OX40L+HK) inhibited their death in the presence of soluble neutral polymers. After the prevention of cell death, YG-PLL proliferated on OX40L+HK without IL2/4 in the presence of two kinds of positively or negatively charged polymers. In particular, dermatan sulfate and poly-L-histidine supported growth for more than 4 months. Therefore, the original lymphoma cells proliferated transiently in the presence of IL2/4, and their growth arrest was inhibited by the addition of PLL. Furthermore, YG-PLL lost IL2/4 dependency by the following 3-step procedure: preculture with IL2/4 and neutral polymers, 3-day culture with neutral polymer on OX40L+HK to inhibit cell death, and co-culture with OX40L+HK in the presence of the positively and negatively charged polymers. The extracellular environment made by soluble polymers plays a role in the growth of ATLL in vitro.

Keywords: Adult T-cell leukemia/lymphoma; Follicular dendritic cell; Interleukin; OX-40 ligand; Soluble high-molecular-weight polymer.

MeSH terms

  • Cell Line, Tumor*
  • Dendritic Cells, Follicular / immunology
  • Dendritic Cells, Follicular / metabolism
  • Dermatan Sulfate / pharmacology*
  • Gene Expression
  • Histidine / pharmacology*
  • Humans
  • Interleukin-2 / metabolism*
  • Interleukin-4 / metabolism*
  • Leukemia-Lymphoma, Adult T-Cell / etiology*
  • Leukemia-Lymphoma, Adult T-Cell / metabolism*
  • Leukemia-Lymphoma, Adult T-Cell / pathology
  • OX40 Ligand / genetics
  • OX40 Ligand / metabolism*

Substances

  • Interleukin-2
  • OX40 Ligand
  • TNFSF4 protein, human
  • Interleukin-4
  • Dermatan Sulfate
  • polyhistidine
  • Histidine