Transforming growth factor β (TGF-β) expression in isolated and cultured rat hepatocytes
It is still a subject of debate whether hepatocytes have the ability to express TGF‐β. Therefore, we investigated in freshly isolated and in monolayer cultures of rat hepatocytes the expression of TGF‐β isoforms at the RNA and protein level applying RT‐PCR, immunocytochemistry, immunoblotting, and f...
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Published in | Journal of cellular physiology Vol. 167; no. 3; pp. 394 - 405 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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01.06.1996
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Abstract | It is still a subject of debate whether hepatocytes have the ability to express TGF‐β. Therefore, we investigated in freshly isolated and in monolayer cultures of rat hepatocytes the expression of TGF‐β isoforms at the RNA and protein level applying RT‐PCR, immunocytochemistry, immunoblotting, and functional assays of TGF‐β, TGF‐β1, ‐β2, and ‐β3 transcripts were detected in cultured cells, and the level of mRNA increased up to 48/72 h, but TGF‐β1 transcripts were absent in freshly isolated cells. Using APAAP stainings the proteins of all three TGF‐β isoforms were observed in hepatocyte cultures from 5–96 h, but in hepatocytes in the liver in situ and in freshly isolated cell suspensions TGF‐β staining was negative. SDS‐PAGE under reducing conditions followed by Western blotting detected in cell lysates the subunit of mature TGF‐β at about 13 kd. Analysis of TGF‐β bioactivity with the mink cell (Mv1Lu) proliferation inhibition assay and competitive radioligand assay confirmed in activated (i.e., acidified and subsequently neutralized) hepatocyte‐conditioned media the presence of TGF‐β, which, however, is almost entirely in the latent form. It is concluded that TGF‐β can be expressed in cultured hepatocytes and that the level of expression is quickly upregulated under abnormal, not yet known, microenvironmental conditions. © 1996 Wiley‐Liss, Inc. |
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AbstractList | It is still a subject of debate whether hepatocytes have the ability to express TGF-beta. Therefore, we investigated in freshly isolated and in monolayer cultures of rat hepatocytes the expression of TGF-beta isoform s at the RNA and protein level applying RT-PCR, immunocytochemistry, immunoblotting, and functional assays of TGF-beta. TFG-beta 1, -beta 2, and -beta 3 transcripts were detected in cultured cells, and the level of m RNA increased up to 48/72 h, but TGF-beta 1 transcripts were absent in freshly isolated cells. Using APAAP stainings the proteins of all three TGF-beta isoforms were observed in hepatocyte cultures from 5-96 h, but in hepatocytes in the liver in situ and in freshly isolated cell suspensions TGF-beta staining was negative. SDS-PAGE under reducing conditions followed by Western blotting detected in cell lysates the subunit of mature TGF-beta at about 13 kd. Analysis of TGF-beta bioactivity with the mink cell (Mv1Lu) proliferation inhibition assay and competitive radioligand assay confirmed in activated (i.e., acidified and subsequently neutralized) hepatocyte-conditioned media the presence of TGF-beta, which, however, is almost entirely in the latent form. It is concluded that TGF-beta can be expressed in cultured hepatocytes and that the level of expression is quickly upregulated under abnormal, not yet known, microenvironmental conditions.It is still a subject of debate whether hepatocytes have the ability to express TGF-beta. Therefore, we investigated in freshly isolated and in monolayer cultures of rat hepatocytes the expression of TGF-beta isoform s at the RNA and protein level applying RT-PCR, immunocytochemistry, immunoblotting, and functional assays of TGF-beta. TFG-beta 1, -beta 2, and -beta 3 transcripts were detected in cultured cells, and the level of m RNA increased up to 48/72 h, but TGF-beta 1 transcripts were absent in freshly isolated cells. Using APAAP stainings the proteins of all three TGF-beta isoforms were observed in hepatocyte cultures from 5-96 h, but in hepatocytes in the liver in situ and in freshly isolated cell suspensions TGF-beta staining was negative. SDS-PAGE under reducing conditions followed by Western blotting detected in cell lysates the subunit of mature TGF-beta at about 13 kd. Analysis of TGF-beta bioactivity with the mink cell (Mv1Lu) proliferation inhibition assay and competitive radioligand assay confirmed in activated (i.e., acidified and subsequently neutralized) hepatocyte-conditioned media the presence of TGF-beta, which, however, is almost entirely in the latent form. It is concluded that TGF-beta can be expressed in cultured hepatocytes and that the level of expression is quickly upregulated under abnormal, not yet known, microenvironmental conditions. It is still a subject of debate whether hepatocytes have the ability to express TGF‐β. Therefore, we investigated in freshly isolated and in monolayer cultures of rat hepatocytes the expression of TGF‐β isoforms at the RNA and protein level applying RT‐PCR, immunocytochemistry, immunoblotting, and functional assays of TGF‐β, TGF‐β1, ‐β2, and ‐β3 transcripts were detected in cultured cells, and the level of mRNA increased up to 48/72 h, but TGF‐β1 transcripts were absent in freshly isolated cells. Using APAAP stainings the proteins of all three TGF‐β isoforms were observed in hepatocyte cultures from 5–96 h, but in hepatocytes in the liver in situ and in freshly isolated cell suspensions TGF‐β staining was negative. SDS‐PAGE under reducing conditions followed by Western blotting detected in cell lysates the subunit of mature TGF‐β at about 13 kd. Analysis of TGF‐β bioactivity with the mink cell (Mv1Lu) proliferation inhibition assay and competitive radioligand assay confirmed in activated (i.e., acidified and subsequently neutralized) hepatocyte‐conditioned media the presence of TGF‐β, which, however, is almost entirely in the latent form. It is concluded that TGF‐β can be expressed in cultured hepatocytes and that the level of expression is quickly upregulated under abnormal, not yet known, microenvironmental conditions. © 1996 Wiley‐Liss, Inc. It is still a subject of debate whether hepatocytes have the ability to express TGF-beta. Therefore, we investigated in freshly isolated and in monolayer cultures of rat hepatocytes the expression of TGF-beta isoform s at the RNA and protein level applying RT-PCR, immunocytochemistry, immunoblotting, and functional assays of TGF-beta. TFG-beta 1, -beta 2, and -beta 3 transcripts were detected in cultured cells, and the level of m RNA increased up to 48/72 h, but TGF-beta 1 transcripts were absent in freshly isolated cells. Using APAAP stainings the proteins of all three TGF-beta isoforms were observed in hepatocyte cultures from 5-96 h, but in hepatocytes in the liver in situ and in freshly isolated cell suspensions TGF-beta staining was negative. SDS-PAGE under reducing conditions followed by Western blotting detected in cell lysates the subunit of mature TGF-beta at about 13 kd. Analysis of TGF-beta bioactivity with the mink cell (Mv1Lu) proliferation inhibition assay and competitive radioligand assay confirmed in activated (i.e., acidified and subsequently neutralized) hepatocyte-conditioned media the presence of TGF-beta, which, however, is almost entirely in the latent form. It is concluded that TGF-beta can be expressed in cultured hepatocytes and that the level of expression is quickly upregulated under abnormal, not yet known, microenvironmental conditions. |
Author | Gressner, G. Gao, Chunfang Gressner, A. M. Zoremba, M. |
Author_xml | – sequence: 1 givenname: Chunfang surname: Gao fullname: Gao, Chunfang organization: Department of Clinical Chemistry and Central Laboratory, Philipps University, Baldingerstrasse, 35033 Marburg, Germany – sequence: 2 givenname: G. surname: Gressner fullname: Gressner, G. organization: Department of Clinical Chemistry and Central Laboratory, Philipps University, Baldingerstrasse, 35033 Marburg, Germany – sequence: 3 givenname: M. surname: Zoremba fullname: Zoremba, M. organization: Department of Clinical Chemistry and Central Laboratory, Philipps University, Baldingerstrasse, 35033 Marburg, Germany – sequence: 4 givenname: A. M. surname: Gressner fullname: Gressner, A. M. organization: Department of Clinical Chemistry and Central Laboratory, Philipps University, Baldingerstrasse, 35033 Marburg, Germany |
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Snippet | It is still a subject of debate whether hepatocytes have the ability to express TGF‐β. Therefore, we investigated in freshly isolated and in monolayer cultures... It is still a subject of debate whether hepatocytes have the ability to express TGF-beta. Therefore, we investigated in freshly isolated and in monolayer... |
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SubjectTerms | Animals Base Sequence Blotting, Western Cells, Cultured Culture Media Electrophoresis, Agar Gel Gene Expression Regulation - genetics Immunoblotting Immunohistochemistry Liver - cytology Liver - metabolism Male Microscopy, Fluorescence Molecular Sequence Data Polymerase Chain Reaction Radioimmunoassay Rats Rats, Sprague-Dawley RNA, Messenger - genetics RNA, Messenger - metabolism Transforming Growth Factor beta - biosynthesis Transforming Growth Factor beta - genetics |
Title | Transforming growth factor β (TGF-β) expression in isolated and cultured rat hepatocytes |
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