In order to investigate the role of Fibroblast Growth Factors in hematopoietic cells, we studied the expression of FGF-1, FGF-2, FGF-3, FGF-4, FGF-5 and FGF-6 mRNAs both in murine myelomonocytic leukemia WEHI-3B and in a murine stromal cell line SR-4987. Secretion of FGF-2 in the cell culture supernatant was also studied. Expression of mRNA encoding for the above-mentioned FGFs was analyzed by RT-PCR. The production of FGF-2 in the conditioned media of WEHI-3B and SR-4987 cell cultures was evaluated by techniques of affinity chromatography, chromatofocusing and immunoblotting. The biological activity of FGF-2 was checked on SR-4987 cells by a agar clonogenic assay. In both cell lines mRNA was found encoding for FGF-1, FGF-2 and FGF-6 and WEHI-3B cells express also mRNA for FGF-3 (int-2) and FGF-4 (K-FGF/hst). Furthermore, supernatant from WEHI-3B cells was found to stimulate dramatically the agar clonogenicity of SR-4987 cells which have a very poor basal capacity for growth in agar. The clonogenic activity of WEHI-3B conditioned medium is due to FGF-2 secreted into cell culture supernatant whereas SR-4987 cells, although express FGF-2 mRNA, do not seem able to secrete this factor. The expression in myeloid leukemia cells of oncogene-related factors such as FGF-3, FGF-4 and FGF-6 together with the secretion of FGF-2 able to support a positive regulation of bone marrow stromal cells function suggest that FGFs may have an important role in sustaining the leukemogenic process and related disorders.

Secretion of basic fibroblast growth factor (FGF-2) by WEHI-3B myelomonocitic leukemia cells / A. Pessina, G. Gagliardi, C. Croera, P. Foti, C. Dassi, P. Brambilla, M.G. Neri. - In: GROWTH FACTORS. - ISSN 0897-7194. - 20:3(2002), pp. 121-129.

Secretion of basic fibroblast growth factor (FGF-2) by WEHI-3B myelomonocitic leukemia cells

A. Pessina;C. Croera;M.G. Neri
2002

Abstract

In order to investigate the role of Fibroblast Growth Factors in hematopoietic cells, we studied the expression of FGF-1, FGF-2, FGF-3, FGF-4, FGF-5 and FGF-6 mRNAs both in murine myelomonocytic leukemia WEHI-3B and in a murine stromal cell line SR-4987. Secretion of FGF-2 in the cell culture supernatant was also studied. Expression of mRNA encoding for the above-mentioned FGFs was analyzed by RT-PCR. The production of FGF-2 in the conditioned media of WEHI-3B and SR-4987 cell cultures was evaluated by techniques of affinity chromatography, chromatofocusing and immunoblotting. The biological activity of FGF-2 was checked on SR-4987 cells by a agar clonogenic assay. In both cell lines mRNA was found encoding for FGF-1, FGF-2 and FGF-6 and WEHI-3B cells express also mRNA for FGF-3 (int-2) and FGF-4 (K-FGF/hst). Furthermore, supernatant from WEHI-3B cells was found to stimulate dramatically the agar clonogenicity of SR-4987 cells which have a very poor basal capacity for growth in agar. The clonogenic activity of WEHI-3B conditioned medium is due to FGF-2 secreted into cell culture supernatant whereas SR-4987 cells, although express FGF-2 mRNA, do not seem able to secrete this factor. The expression in myeloid leukemia cells of oncogene-related factors such as FGF-3, FGF-4 and FGF-6 together with the secretion of FGF-2 able to support a positive regulation of bone marrow stromal cells function suggest that FGFs may have an important role in sustaining the leukemogenic process and related disorders.
English
Anchorage dependency; FGF-2; Fibroblast growth factors; SR-4987 stromal cells; WEHI-3B myelomonocytic leukemia
Settore MED/07 - Microbiologia e Microbiologia Clinica
Articolo
Sì, ma tipo non specificato
2002
Taylor & Francis
20
3
121
129
Periodico con rilevanza internazionale
info:eu-repo/semantics/article
Secretion of basic fibroblast growth factor (FGF-2) by WEHI-3B myelomonocitic leukemia cells / A. Pessina, G. Gagliardi, C. Croera, P. Foti, C. Dassi, P. Brambilla, M.G. Neri. - In: GROWTH FACTORS. - ISSN 0897-7194. - 20:3(2002), pp. 121-129.
none
Prodotti della ricerca::01 - Articolo su periodico
7
262
Article (author)
si
A. Pessina, G. Gagliardi, C. Croera, P. Foti, C. Dassi, P. Brambilla, M.G. Neri
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/41435
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