Modulation of milk protein synthesis through alteration of the cytoskeleton in mouse mammary epithelial cells cultured on a reconstituted basement membrane
Recent studies indicate that the cytoskeleton may be involved in modulating tissue‐specific gene expression in mammalian cells. We have studied the role of the cytoskeleton in regulating milk protein synthesis and secretion by primary mouse mammary epithelial cells cultured on a reconstituted baseme...
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Veröffentlicht in: | Journal of cellular physiology 1991-01, Vol.146 (1), p.117-130 |
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description | Recent studies indicate that the cytoskeleton may be involved in modulating tissue‐specific gene expression in mammalian cells. We have studied the role of the cytoskeleton in regulating milk protein synthesis and secretion by primary mouse mammary epithelial cells cultured on a reconstituted basement membrane that promotes differentiation. After 8 days in culture, cells were treated with cytochalasin D (CD) (0.5–1 μg/ml) to alter actin filaments or acrylamide (Ac) (5 mM) to alter intermediate filaments (cytokeratins). CD inhibited synthesis of most proteins in a concentration‐dependent manner, with β‐casein being the first affected. In contrast, Ac increased protein synthesis and secretion by 17–31% after a 12 hr treatment. Polyacrylamide gel electrophoresis of total secreted proteins indicates that synthetic rates of most proteins were increased equally by Ac treatment. This increase is apparently controlled at the level of translation, because control and Ac‐treated cells contained the same amount of poly‐A+ RNA, and neither CD nor Ac altered mRNA levels for β‐casein. There was also no indication that either CD or Ac can induce the expression of milk proteins in quiescent cells cultured on a plastic substratum. In conjunction with the biochemical studies, changes in cytoskeletal morphology caused by the drug treatments were analyzed by immunofluorescence microscopy. As has been observed in other cell types, low concentrations of CD caused cells to round up by disrupting actin filaments. Ac treatment slightly decreased the intensity of actin staining, but no changes in microfilament organization were observed. Ac‐treated cells showed slight disorganization of the cytokeratin filaments, with some peripheral interfibrillar bundling, but the cytokeratin network did not collapse and no retraction of cell extensions or breakdown of cell‐cell contacts was observed. These results confirm previous reports that the actin cytoskeleton may play a role in regulating tissue‐specific protein synthesis. How Ac stimulates protein synthesis is unknown, but it is unlikely that this effect is directly mediated through intermediate filaments. |
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We have studied the role of the cytoskeleton in regulating milk protein synthesis and secretion by primary mouse mammary epithelial cells cultured on a reconstituted basement membrane that promotes differentiation. After 8 days in culture, cells were treated with cytochalasin D (CD) (0.5–1 μg/ml) to alter actin filaments or acrylamide (Ac) (5 mM) to alter intermediate filaments (cytokeratins). CD inhibited synthesis of most proteins in a concentration‐dependent manner, with β‐casein being the first affected. In contrast, Ac increased protein synthesis and secretion by 17–31% after a 12 hr treatment. Polyacrylamide gel electrophoresis of total secreted proteins indicates that synthetic rates of most proteins were increased equally by Ac treatment. This increase is apparently controlled at the level of translation, because control and Ac‐treated cells contained the same amount of poly‐A+ RNA, and neither CD nor Ac altered mRNA levels for β‐casein. There was also no indication that either CD or Ac can induce the expression of milk proteins in quiescent cells cultured on a plastic substratum. In conjunction with the biochemical studies, changes in cytoskeletal morphology caused by the drug treatments were analyzed by immunofluorescence microscopy. As has been observed in other cell types, low concentrations of CD caused cells to round up by disrupting actin filaments. Ac treatment slightly decreased the intensity of actin staining, but no changes in microfilament organization were observed. Ac‐treated cells showed slight disorganization of the cytokeratin filaments, with some peripheral interfibrillar bundling, but the cytokeratin network did not collapse and no retraction of cell extensions or breakdown of cell‐cell contacts was observed. These results confirm previous reports that the actin cytoskeleton may play a role in regulating tissue‐specific protein synthesis. How Ac stimulates protein synthesis is unknown, but it is unlikely that this effect is directly mediated through intermediate filaments.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.1041460116</identifier><identifier>PMID: 1990014</identifier><identifier>CODEN: JCLLAX</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Acrylamide ; Acrylamides - pharmacology ; Animals ; Basement Membrane - physiology ; Biological and medical sciences ; Cells, Cultured ; Collagen ; Cytochalasin D - pharmacology ; Cytoskeleton - drug effects ; Cytoskeleton - physiology ; Drug Combinations ; Epithelium - drug effects ; Epithelium - metabolism ; Epithelium - secretion ; Female ; Fundamental and applied biological sciences. Psychology ; Laminin ; Mammary Glands, Animal - drug effects ; Mammary Glands, Animal - metabolism ; Mammary Glands, Animal - secretion ; Mice ; Milk Proteins - biosynthesis ; Milk Proteins - secretion ; Molecular and cellular biology ; Molecular genetics ; Precipitin Tests ; Pregnancy ; Protein Biosynthesis - drug effects ; Proteoglycans ; RNA, Messenger - metabolism ; Transcription. Transcription factor. Splicing. 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Cell. Physiol</addtitle><description>Recent studies indicate that the cytoskeleton may be involved in modulating tissue‐specific gene expression in mammalian cells. We have studied the role of the cytoskeleton in regulating milk protein synthesis and secretion by primary mouse mammary epithelial cells cultured on a reconstituted basement membrane that promotes differentiation. After 8 days in culture, cells were treated with cytochalasin D (CD) (0.5–1 μg/ml) to alter actin filaments or acrylamide (Ac) (5 mM) to alter intermediate filaments (cytokeratins). CD inhibited synthesis of most proteins in a concentration‐dependent manner, with β‐casein being the first affected. In contrast, Ac increased protein synthesis and secretion by 17–31% after a 12 hr treatment. Polyacrylamide gel electrophoresis of total secreted proteins indicates that synthetic rates of most proteins were increased equally by Ac treatment. This increase is apparently controlled at the level of translation, because control and Ac‐treated cells contained the same amount of poly‐A+ RNA, and neither CD nor Ac altered mRNA levels for β‐casein. There was also no indication that either CD or Ac can induce the expression of milk proteins in quiescent cells cultured on a plastic substratum. In conjunction with the biochemical studies, changes in cytoskeletal morphology caused by the drug treatments were analyzed by immunofluorescence microscopy. As has been observed in other cell types, low concentrations of CD caused cells to round up by disrupting actin filaments. Ac treatment slightly decreased the intensity of actin staining, but no changes in microfilament organization were observed. Ac‐treated cells showed slight disorganization of the cytokeratin filaments, with some peripheral interfibrillar bundling, but the cytokeratin network did not collapse and no retraction of cell extensions or breakdown of cell‐cell contacts was observed. These results confirm previous reports that the actin cytoskeleton may play a role in regulating tissue‐specific protein synthesis. How Ac stimulates protein synthesis is unknown, but it is unlikely that this effect is directly mediated through intermediate filaments.</description><subject>Acrylamide</subject><subject>Acrylamides - pharmacology</subject><subject>Animals</subject><subject>Basement Membrane - physiology</subject><subject>Biological and medical sciences</subject><subject>Cells, Cultured</subject><subject>Collagen</subject><subject>Cytochalasin D - pharmacology</subject><subject>Cytoskeleton - drug effects</subject><subject>Cytoskeleton - physiology</subject><subject>Drug Combinations</subject><subject>Epithelium - drug effects</subject><subject>Epithelium - metabolism</subject><subject>Epithelium - secretion</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Laminin</subject><subject>Mammary Glands, Animal - drug effects</subject><subject>Mammary Glands, Animal - metabolism</subject><subject>Mammary Glands, Animal - secretion</subject><subject>Mice</subject><subject>Milk Proteins - biosynthesis</subject><subject>Milk Proteins - secretion</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Precipitin Tests</subject><subject>Pregnancy</subject><subject>Protein Biosynthesis - drug effects</subject><subject>Proteoglycans</subject><subject>RNA, Messenger - metabolism</subject><subject>Transcription. Transcription factor. Splicing. Rna processing</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2PFCEQhonRrOPq1ZsJB-OtV2joD45msq4f60fMGr0Rmi4cdqAZgY7Ob_HPyqQns_HkiUrV8xb1ViH0lJILSkj98lbvSsApbwml7T20okR0FW-b-j5aFYBWouH0IXqU0i0hRAjGztAZFYIQylfoz4cwzk5lGyYcDPbWbfEuhgx2wmk_5Q0km3DexDD_2GDlMsQTXIpY73NIW3CQS65ofJgTYK-8V3GPYWcL5KxyWINzCevZ5TnCiAutcAQdppRtnnNJDSqBhyljD36IaoLH6IFRLsGT43uOvr6-vFm_qa4_Xb1dv7quNCddW9FBAAg-6n4wnWE1G2teIqEMF2Upho-mo4rWjeaqHfnYkNrA0I1dz4C2DNg5erH0LcZ_zpCy9DYd5i0zFDuyJ7zuWd8U8GIBdQwpRTByF-3BqKREHq4hyzXk3TWK4Nmx8zx4GO_wZf2l_vxYV0krZ4prbdMJ44LzphcFEwv2yzrY_-dT-W79-Z8RqkVrU4bfJ62KW9l2rGvkt49X8su662_671y-Z38BdDO2zA</recordid><startdate>199101</startdate><enddate>199101</enddate><creator>Seely, Keith A.</creator><creator>Aggeler, Judith</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199101</creationdate><title>Modulation of milk protein synthesis through alteration of the cytoskeleton in mouse mammary epithelial cells cultured on a reconstituted basement membrane</title><author>Seely, Keith A. ; Aggeler, Judith</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4076-1b9ee94dc8bf7f323d24bf79af49601f4df71a125c4a6d4d502feb7d783e163e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Acrylamide</topic><topic>Acrylamides - pharmacology</topic><topic>Animals</topic><topic>Basement Membrane - physiology</topic><topic>Biological and medical sciences</topic><topic>Cells, Cultured</topic><topic>Collagen</topic><topic>Cytochalasin D - pharmacology</topic><topic>Cytoskeleton - drug effects</topic><topic>Cytoskeleton - physiology</topic><topic>Drug Combinations</topic><topic>Epithelium - drug effects</topic><topic>Epithelium - metabolism</topic><topic>Epithelium - secretion</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Laminin</topic><topic>Mammary Glands, Animal - drug effects</topic><topic>Mammary Glands, Animal - metabolism</topic><topic>Mammary Glands, Animal - secretion</topic><topic>Mice</topic><topic>Milk Proteins - biosynthesis</topic><topic>Milk Proteins - secretion</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Precipitin Tests</topic><topic>Pregnancy</topic><topic>Protein Biosynthesis - drug effects</topic><topic>Proteoglycans</topic><topic>RNA, Messenger - metabolism</topic><topic>Transcription. Transcription factor. Splicing. Rna processing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seely, Keith A.</creatorcontrib><creatorcontrib>Aggeler, Judith</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cellular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seely, Keith A.</au><au>Aggeler, Judith</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modulation of milk protein synthesis through alteration of the cytoskeleton in mouse mammary epithelial cells cultured on a reconstituted basement membrane</atitle><jtitle>Journal of cellular physiology</jtitle><addtitle>J. Cell. Physiol</addtitle><date>1991-01</date><risdate>1991</risdate><volume>146</volume><issue>1</issue><spage>117</spage><epage>130</epage><pages>117-130</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><coden>JCLLAX</coden><abstract>Recent studies indicate that the cytoskeleton may be involved in modulating tissue‐specific gene expression in mammalian cells. We have studied the role of the cytoskeleton in regulating milk protein synthesis and secretion by primary mouse mammary epithelial cells cultured on a reconstituted basement membrane that promotes differentiation. After 8 days in culture, cells were treated with cytochalasin D (CD) (0.5–1 μg/ml) to alter actin filaments or acrylamide (Ac) (5 mM) to alter intermediate filaments (cytokeratins). CD inhibited synthesis of most proteins in a concentration‐dependent manner, with β‐casein being the first affected. In contrast, Ac increased protein synthesis and secretion by 17–31% after a 12 hr treatment. Polyacrylamide gel electrophoresis of total secreted proteins indicates that synthetic rates of most proteins were increased equally by Ac treatment. This increase is apparently controlled at the level of translation, because control and Ac‐treated cells contained the same amount of poly‐A+ RNA, and neither CD nor Ac altered mRNA levels for β‐casein. There was also no indication that either CD or Ac can induce the expression of milk proteins in quiescent cells cultured on a plastic substratum. In conjunction with the biochemical studies, changes in cytoskeletal morphology caused by the drug treatments were analyzed by immunofluorescence microscopy. As has been observed in other cell types, low concentrations of CD caused cells to round up by disrupting actin filaments. Ac treatment slightly decreased the intensity of actin staining, but no changes in microfilament organization were observed. Ac‐treated cells showed slight disorganization of the cytokeratin filaments, with some peripheral interfibrillar bundling, but the cytokeratin network did not collapse and no retraction of cell extensions or breakdown of cell‐cell contacts was observed. These results confirm previous reports that the actin cytoskeleton may play a role in regulating tissue‐specific protein synthesis. How Ac stimulates protein synthesis is unknown, but it is unlikely that this effect is directly mediated through intermediate filaments.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>1990014</pmid><doi>10.1002/jcp.1041460116</doi><tpages>14</tpages></addata></record> |
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subjects | Acrylamide Acrylamides - pharmacology Animals Basement Membrane - physiology Biological and medical sciences Cells, Cultured Collagen Cytochalasin D - pharmacology Cytoskeleton - drug effects Cytoskeleton - physiology Drug Combinations Epithelium - drug effects Epithelium - metabolism Epithelium - secretion Female Fundamental and applied biological sciences. Psychology Laminin Mammary Glands, Animal - drug effects Mammary Glands, Animal - metabolism Mammary Glands, Animal - secretion Mice Milk Proteins - biosynthesis Milk Proteins - secretion Molecular and cellular biology Molecular genetics Precipitin Tests Pregnancy Protein Biosynthesis - drug effects Proteoglycans RNA, Messenger - metabolism Transcription. Transcription factor. Splicing. Rna processing |
title | Modulation of milk protein synthesis through alteration of the cytoskeleton in mouse mammary epithelial cells cultured on a reconstituted basement membrane |
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