The Medium Obtained from the Culture of Hodgkin Lymphoma Cells Affects the Biophysical Characteristics of a Fibroblast Cell Model

Author:

Rossi Maura1,Alviano Francesco1ORCID,Myrtaj Barie1,Zia Silvia2,Righi Simona1,Pizzuti Valeria1ORCID,Paris Francesca1ORCID,Roda Barbara23ORCID,Zattoni Andrea23ORCID,Bonsi Laura1,Sabattini Elena4ORCID,Agostinelli Claudio14

Affiliation:

1. Department of Medical and Surgical Sciences, University of Bologna, 40138 Bologna, Italy

2. Stem Sel srl, 40127 Bologna, Italy

3. Department of Chemistry “G. Ciamician”, University of Bologna, 40126 Bologna, Italy

4. Haematopathology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy

Abstract

The neoplastic Hodgkin-Reed-Sternberg (HRS) cells in Hodgkin lymphoma (HL) represent only 1–10% of cells and are surrounded by an inflammatory microenvironment. The HL cytokine network is a key point for the proliferation of HRS cells and for the maintenance of an advantageous microenvironment for HRS survival. In the tumor microenvironment (TME), the fibroblasts are involved in crosstalk with HRS cells. The aim of this work was to study the effect of lymphoma cell conditioned medium on a fibroblast cell population and evaluate modifications of cell morphology and proliferation. Hodgkin lymphoma-derived medium was used to obtain a population of “conditioned” fibroblasts (WS-1 COND). Differences in biophysical parameters were detected by the innovative device Celector®. Fibroblast-HL cells interactions were reproduced in 3D co-culture spheroids. WS-1 COND showed a different cellular morphology with an enlarged cytoplasm and enhanced metabolism. Area and diameter cell values obtained by Celector® measurement were increased. Co-culture spheroids created with WS-1 COND showed a tighter aggregation than those with non-conditioned WS-1. The presence of soluble factors derived from HRS cells in the conditioned medium was adequate for the proliferation of fibroblasts and conditioned fibroblasts in a 3D HL model allowed to develop a representative model of the in vivo TME.

Publisher

MDPI AG

Subject

Bioengineering

Reference40 articles.

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