Formation of apical tubules from large endocytic vacuoles in kidney proximal tubule cells during absorption of horseradish peroxidase
Using horseradish peroxidase (HRP) as a tracer, we have investigated if the so-called apical tubules (AT) in the kidney proximal tubule cells are directly involved in the endocytic process by carrying the tracer into the cells, or if they are derived from the intracellular membrane compartments. Rat...
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Veröffentlicht in: | Cell and tissue research 1986-11, Vol.246 (2), p.271-278 |
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description | Using horseradish peroxidase (HRP) as a tracer, we have investigated if the so-called apical tubules (AT) in the kidney proximal tubule cells are directly involved in the endocytic process by carrying the tracer into the cells, or if they are derived from the intracellular membrane compartments. Rat kidney was fixed by vascular perfusion at different time intervals after intravenous injection of HRP and prepared for electron microscopy. An analysis revealed that 0.5 min after injection, invaginations of the plasma membrane and small apical endocytic vesicles, including coated vesicles, were labelled with reaction product, whereas almost all large apical endocytic vacuoles and the AT were negative. The endocytic vacuoles and about 18% of the AT were labelled 1 min after injection. The reaction product in the large endocytic vacuoles was usually seen along the luminal surface of the vacuoles. The AT with reaction product appeared as a branched network, and were frequently connected with the labelled endocytic vacuoles. Three min after injection, reaction product was detected in about 38% of the AT, and thereafter, the percentage increased to about 74% after 7 min. No reaction product was detected in the Golgi complex at any time after HRP-injection. These findings indicate that the AT are probably formed by budding off from the large endocytic vacuoles, rather than being directly involved in the endocytic process. |
doi_str_mv | 10.1007/bf00215889 |
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Rat kidney was fixed by vascular perfusion at different time intervals after intravenous injection of HRP and prepared for electron microscopy. An analysis revealed that 0.5 min after injection, invaginations of the plasma membrane and small apical endocytic vesicles, including coated vesicles, were labelled with reaction product, whereas almost all large apical endocytic vacuoles and the AT were negative. The endocytic vacuoles and about 18% of the AT were labelled 1 min after injection. The reaction product in the large endocytic vacuoles was usually seen along the luminal surface of the vacuoles. The AT with reaction product appeared as a branched network, and were frequently connected with the labelled endocytic vacuoles. Three min after injection, reaction product was detected in about 38% of the AT, and thereafter, the percentage increased to about 74% after 7 min. No reaction product was detected in the Golgi complex at any time after HRP-injection. These findings indicate that the AT are probably formed by budding off from the large endocytic vacuoles, rather than being directly involved in the endocytic process.</description><identifier>ISSN: 0302-766X</identifier><identifier>EISSN: 1432-0878</identifier><identifier>DOI: 10.1007/bf00215889</identifier><identifier>PMID: 3779809</identifier><identifier>CODEN: CTSRCS</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Absorption ; Animals ; Biological and medical sciences ; Endocytosis ; Fundamental and applied biological sciences. Psychology ; Horseradish Peroxidase - metabolism ; In Vitro Techniques ; Kidney Tubules, Proximal - physiology ; Kidney Tubules, Proximal - ultrastructure ; Male ; Microscopy, Electron ; Rats ; Rats, Inbred Strains ; Vacuoles - physiology ; Vacuoles - ultrastructure ; Vertebrates: urinary system</subject><ispartof>Cell and tissue research, 1986-11, Vol.246 (2), p.271-278</ispartof><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c377t-4822058029511c7c7ab2744023f904e784993f43015e235250cee282d70141a43</citedby><cites>FETCH-LOGICAL-c377t-4822058029511c7c7ab2744023f904e784993f43015e235250cee282d70141a43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8283814$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3779809$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HATAE, T</creatorcontrib><creatorcontrib>FUJITA, M</creatorcontrib><creatorcontrib>SAGARA, H</creatorcontrib><creatorcontrib>OKUYAMA, K</creatorcontrib><title>Formation of apical tubules from large endocytic vacuoles in kidney proximal tubule cells during absorption of horseradish peroxidase</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><description>Using horseradish peroxidase (HRP) as a tracer, we have investigated if the so-called apical tubules (AT) in the kidney proximal tubule cells are directly involved in the endocytic process by carrying the tracer into the cells, or if they are derived from the intracellular membrane compartments. Rat kidney was fixed by vascular perfusion at different time intervals after intravenous injection of HRP and prepared for electron microscopy. An analysis revealed that 0.5 min after injection, invaginations of the plasma membrane and small apical endocytic vesicles, including coated vesicles, were labelled with reaction product, whereas almost all large apical endocytic vacuoles and the AT were negative. The endocytic vacuoles and about 18% of the AT were labelled 1 min after injection. The reaction product in the large endocytic vacuoles was usually seen along the luminal surface of the vacuoles. The AT with reaction product appeared as a branched network, and were frequently connected with the labelled endocytic vacuoles. Three min after injection, reaction product was detected in about 38% of the AT, and thereafter, the percentage increased to about 74% after 7 min. No reaction product was detected in the Golgi complex at any time after HRP-injection. These findings indicate that the AT are probably formed by budding off from the large endocytic vacuoles, rather than being directly involved in the endocytic process.</description><subject>Absorption</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Endocytosis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Horseradish Peroxidase - metabolism</subject><subject>In Vitro Techniques</subject><subject>Kidney Tubules, Proximal - physiology</subject><subject>Kidney Tubules, Proximal - ultrastructure</subject><subject>Male</subject><subject>Microscopy, Electron</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Vacuoles - physiology</subject><subject>Vacuoles - ultrastructure</subject><subject>Vertebrates: urinary system</subject><issn>0302-766X</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kb1O7DAQhS0Egr1AQ4_kAlFcKTD-ydopAbFwJSQakOgix5mAIYmDnVyxD8B74xW7W01xzsyc-YaQEwYXDEBdVg0AZ7nWxQ6ZMSl4BlrpXTIDATxT8_nLAfkT4zsAk_N5sU_2hVKFhmJGvhc-dGZ0vqe-oWZw1rR0nKqpxUib4DvamvCKFPva2-XoLP1v7ORXquvph6t7XNIh-C_XbRupxbaNtJ6C61-pqaIPw2bDmw8Rg6ldfKMDrvpqE_GI7DWmjXi8rofkeXH7dHOfPTze_bu5eshsCjxmUnMOuQZe5IxZZZWpuJISuGgKkKi0LArRSAEsRy5ynoNF5JrXKh3OjBSH5Px3bkr8OWEcy87FVVrTo59iqVSiyLRKxr-_Rht8jAGbcgjpwrAsGZQr5uX1YsM8mU_XU6eqw3prXUNO-tlaNzHhbYLprYtbm-Za6PS1H1Z3ieI</recordid><startdate>198611</startdate><enddate>198611</enddate><creator>HATAE, T</creator><creator>FUJITA, M</creator><creator>SAGARA, H</creator><creator>OKUYAMA, K</creator><general>Springer</general><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>198611</creationdate><title>Formation of apical tubules from large endocytic vacuoles in kidney proximal tubule cells during absorption of horseradish peroxidase</title><author>HATAE, T ; FUJITA, M ; SAGARA, H ; OKUYAMA, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c377t-4822058029511c7c7ab2744023f904e784993f43015e235250cee282d70141a43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Absorption</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Endocytosis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Horseradish Peroxidase - metabolism</topic><topic>In Vitro Techniques</topic><topic>Kidney Tubules, Proximal - physiology</topic><topic>Kidney Tubules, Proximal - ultrastructure</topic><topic>Male</topic><topic>Microscopy, Electron</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Vacuoles - physiology</topic><topic>Vacuoles - ultrastructure</topic><topic>Vertebrates: urinary system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HATAE, T</creatorcontrib><creatorcontrib>FUJITA, M</creatorcontrib><creatorcontrib>SAGARA, H</creatorcontrib><creatorcontrib>OKUYAMA, K</creatorcontrib><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>Cell and tissue research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HATAE, T</au><au>FUJITA, M</au><au>SAGARA, H</au><au>OKUYAMA, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Formation of apical tubules from large endocytic vacuoles in kidney proximal tubule cells during absorption of horseradish peroxidase</atitle><jtitle>Cell and tissue research</jtitle><addtitle>Cell Tissue Res</addtitle><date>1986-11</date><risdate>1986</risdate><volume>246</volume><issue>2</issue><spage>271</spage><epage>278</epage><pages>271-278</pages><issn>0302-766X</issn><eissn>1432-0878</eissn><coden>CTSRCS</coden><abstract>Using horseradish peroxidase (HRP) as a tracer, we have investigated if the so-called apical tubules (AT) in the kidney proximal tubule cells are directly involved in the endocytic process by carrying the tracer into the cells, or if they are derived from the intracellular membrane compartments. Rat kidney was fixed by vascular perfusion at different time intervals after intravenous injection of HRP and prepared for electron microscopy. An analysis revealed that 0.5 min after injection, invaginations of the plasma membrane and small apical endocytic vesicles, including coated vesicles, were labelled with reaction product, whereas almost all large apical endocytic vacuoles and the AT were negative. The endocytic vacuoles and about 18% of the AT were labelled 1 min after injection. The reaction product in the large endocytic vacuoles was usually seen along the luminal surface of the vacuoles. The AT with reaction product appeared as a branched network, and were frequently connected with the labelled endocytic vacuoles. Three min after injection, reaction product was detected in about 38% of the AT, and thereafter, the percentage increased to about 74% after 7 min. No reaction product was detected in the Golgi complex at any time after HRP-injection. These findings indicate that the AT are probably formed by budding off from the large endocytic vacuoles, rather than being directly involved in the endocytic process.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>3779809</pmid><doi>10.1007/bf00215889</doi><tpages>8</tpages></addata></record> |
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subjects | Absorption Animals Biological and medical sciences Endocytosis Fundamental and applied biological sciences. Psychology Horseradish Peroxidase - metabolism In Vitro Techniques Kidney Tubules, Proximal - physiology Kidney Tubules, Proximal - ultrastructure Male Microscopy, Electron Rats Rats, Inbred Strains Vacuoles - physiology Vacuoles - ultrastructure Vertebrates: urinary system |
title | Formation of apical tubules from large endocytic vacuoles in kidney proximal tubule cells during absorption of horseradish peroxidase |
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