1985
DOI: 10.1007/bf00320927
|View full text |Cite
|
Sign up to set email alerts
|

Thymosin ?4 induced phenotypic changes in Molt-4 leukemic cell line

Abstract: Thymosin beta 4 was tested for its ability to induce phenotypic changes in the human T-cell line Molt-4. Cells were cultured with nanogram concentrations of thymosin beta 4 for up to 16 days and were analyzed with a panel of monoclonal antibodies, sheep erythrocyte rosetting, peanut agglutinin binding (PNA) and an antibody to the enzyme, terminal deoxynucleotidyl transferase (TdT). Thymosin beta 4 induced Molt-4 cells to reduce the expression of a T-cell lineage specific antigen, with preferential expression o… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
6
0

Year Published

1987
1987
2022
2022

Publication Types

Select...
8
2

Relationship

0
10

Authors

Journals

citations
Cited by 16 publications
(6 citation statements)
references
References 28 publications
0
6
0
Order By: Relevance
“…It was reported that the mRNA encoding Tβ4 was increased rapidly in tumor cells and the overexpression of Tβ4 could promote the cell grow and migrate [ 39 ]. However, application of β-thymosin could not repair the damaged skin of animals [ 40 ], and the β-thymosin could turn tumor cells into normal cells [ 41 ], indicating it has no or even inhibitory effects on cell proliferation. In this study, the BmTHY1 seems to have stronger effects to stimulate cell proliferation than BmTHY2 ( Fig 8 ), although both have similar stimulating effects on cell migration ( Fig 8 ), which is consistent with Tβ4’s role in the regulation of G-actin polymerization and depolymerization [ 9 , 10 ].…”
Section: Discussionmentioning
confidence: 99%
“…It was reported that the mRNA encoding Tβ4 was increased rapidly in tumor cells and the overexpression of Tβ4 could promote the cell grow and migrate [ 39 ]. However, application of β-thymosin could not repair the damaged skin of animals [ 40 ], and the β-thymosin could turn tumor cells into normal cells [ 41 ], indicating it has no or even inhibitory effects on cell proliferation. In this study, the BmTHY1 seems to have stronger effects to stimulate cell proliferation than BmTHY2 ( Fig 8 ), although both have similar stimulating effects on cell migration ( Fig 8 ), which is consistent with Tβ4’s role in the regulation of G-actin polymerization and depolymerization [ 9 , 10 ].…”
Section: Discussionmentioning
confidence: 99%
“…It is a 43-aminoacid polypeptide that was originally described as a thymic maturation factor (Low et al, 1981). It was reported that Tb4 could suppress the mixed lymphocyte proliferative response, induce the expression of terminal deoxynucleotidyl transferase in T cells, inhibit the migration of macrophages in vitro and induce the phenotypic changes in T cell line (Baxevanis et al, 1987;Kokkinopoulos et al, 1985). Recently, it was reported that Tb4 promotes angiogenesis, wound repair, and hair follicle development (Philp et al, 2004); stimulates tumor metastasis by activating cell migration and angiogenesis (Cha et al, 2003;Liu et al, 2003;Wang et al, 2004).…”
Section: Introductionmentioning
confidence: 99%
“…The peptide is widely distributed in numerous tissues (Horecker & Morgan, 1981; Goodall et al, 1983;Hannappel, 1986) and in recent years different /3-thymosins were isolated from many species ranging from sea urchin (Schmid et al, 1989) to mammals (Hannappel, 1986). Thymosin /34 has been reported to induce terminal deoxynucleotidyl transferase activity in vivo and in vitro (Low et al, 1981), inhibit the migration of guinea pig peritoneal macrophages (Thurman et al, 1981), stimulate the hypothalamic secretion of luteinizing hormone releasing factor (Rebar et al, 1981), or induce phenotypic changes in the Molt-4 leukemic cell line (Kokkinopoulos et al, 1985).…”
mentioning
confidence: 99%