Expression and distribution of the Kit receptor in bovine bone marrow cells

To characterize the expression and distribution of the Kit receptor in bovine bone marrow cells (BMC) and to define the function of its ligand, stem cell factor (SCF). Six 7- to 70-day-old healthy male Holstein-Friesian calves. Expression and distribution of the Kit receptor were assessed by use of...

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Veröffentlicht in:American journal of veterinary research 2001-06, Vol.62 (6), p.974-977
Hauptverfasser: Hikono, H, Ohta, M, Zhou, J H, Sakurai, M
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container_title American journal of veterinary research
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creator Hikono, H
Ohta, M
Zhou, J H
Sakurai, M
description To characterize the expression and distribution of the Kit receptor in bovine bone marrow cells (BMC) and to define the function of its ligand, stem cell factor (SCF). Six 7- to 70-day-old healthy male Holstein-Friesian calves. Expression and distribution of the Kit receptor were assessed by use of flow cytometry with monoclonal antibodies (mAb) against the bovine Kit protein. Using Giemsa-stained centrifuged preparations, the histologic appearance of Kit receptor positive (Kit+) BMC were evaluated. Semisolid cultures supplemented with granulocyte colony-stimulating factor (G-CSF) and SCF were used to measure the colony formation capacity of Kit+ BMC. The Kit receptor was expressed on approximately 18% of total BMC. Most of Kit+ BMC did not coexpress lineage markers, but a small subset of this population did coexpress CD3. The Kit+CD3- BMC were a heterogeneous cell population comprising blast-like cells such as myeloblasts, promyelocytes, rubriblasts, and prorubricytes. Conversely, Kit+CD3+ BMC had a lymphocyte-like appearance. Kit+ BMC formed colonies in semisolid culture with G-CSF, whereas Kit- BMC failed to grow. Addition of SCF to G-CSF resulted in superadditive enhancement in colony numbers and size. The Kit receptor is expressed primarily on immature blood cells in bovine bone marrow, and Kit+ BMC contain hematopoietic progenitor cells that are reactive to G-CSF. In addition, SCF synergizes with G-CSF to stimulate colony formation by these cells. Our results suggest that the Kit receptor and its ligand, SCF, are involved in early stages of granulopoiesis in calves.
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Six 7- to 70-day-old healthy male Holstein-Friesian calves. Expression and distribution of the Kit receptor were assessed by use of flow cytometry with monoclonal antibodies (mAb) against the bovine Kit protein. Using Giemsa-stained centrifuged preparations, the histologic appearance of Kit receptor positive (Kit+) BMC were evaluated. Semisolid cultures supplemented with granulocyte colony-stimulating factor (G-CSF) and SCF were used to measure the colony formation capacity of Kit+ BMC. The Kit receptor was expressed on approximately 18% of total BMC. Most of Kit+ BMC did not coexpress lineage markers, but a small subset of this population did coexpress CD3. The Kit+CD3- BMC were a heterogeneous cell population comprising blast-like cells such as myeloblasts, promyelocytes, rubriblasts, and prorubricytes. Conversely, Kit+CD3+ BMC had a lymphocyte-like appearance. Kit+ BMC formed colonies in semisolid culture with G-CSF, whereas Kit- BMC failed to grow. Addition of SCF to G-CSF resulted in superadditive enhancement in colony numbers and size. The Kit receptor is expressed primarily on immature blood cells in bovine bone marrow, and Kit+ BMC contain hematopoietic progenitor cells that are reactive to G-CSF. In addition, SCF synergizes with G-CSF to stimulate colony formation by these cells. 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Six 7- to 70-day-old healthy male Holstein-Friesian calves. Expression and distribution of the Kit receptor were assessed by use of flow cytometry with monoclonal antibodies (mAb) against the bovine Kit protein. Using Giemsa-stained centrifuged preparations, the histologic appearance of Kit receptor positive (Kit+) BMC were evaluated. Semisolid cultures supplemented with granulocyte colony-stimulating factor (G-CSF) and SCF were used to measure the colony formation capacity of Kit+ BMC. The Kit receptor was expressed on approximately 18% of total BMC. Most of Kit+ BMC did not coexpress lineage markers, but a small subset of this population did coexpress CD3. The Kit+CD3- BMC were a heterogeneous cell population comprising blast-like cells such as myeloblasts, promyelocytes, rubriblasts, and prorubricytes. Conversely, Kit+CD3+ BMC had a lymphocyte-like appearance. Kit+ BMC formed colonies in semisolid culture with G-CSF, whereas Kit- BMC failed to grow. Addition of SCF to G-CSF resulted in superadditive enhancement in colony numbers and size. The Kit receptor is expressed primarily on immature blood cells in bovine bone marrow, and Kit+ BMC contain hematopoietic progenitor cells that are reactive to G-CSF. In addition, SCF synergizes with G-CSF to stimulate colony formation by these cells. Our results suggest that the Kit receptor and its ligand, SCF, are involved in early stages of granulopoiesis in calves.</description><subject>Animals</subject><subject>Bone Marrow Cells - metabolism</subject><subject>Cattle - metabolism</subject><subject>Cattle - physiology</subject><subject>Flow Cytometry - veterinary</subject><subject>Granulocyte Colony-Stimulating Factor - physiology</subject><subject>Male</subject><subject>Proto-Oncogene Proteins c-kit - biosynthesis</subject><subject>Proto-Oncogene Proteins c-kit - metabolism</subject><subject>Stem Cell Factor - physiology</subject><issn>0002-9645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkL1PwzAQxT2AaPnYmVAmtpSz4zjxiKryoVZigdmynbNw1cbBTgr89yRqJZZ70t17p6cfIbcUFowLeNDbQ1wwALoQbCErfkbmAMByKXg5I5cpbccbq2l5QWaUcoC6lHOyXv10EVPyoc1022SNT330ZuinRXBZ_4nZ2vdZRItdH2Lm28yEg29xlHHsdYzhO7O426Vrcu70LuHNSa_Ix9PqffmSb96eX5ePm9wyWfY516hrIWxVUwQwDGWjecVKzQ0KV9mCGonOScbBQFNZHO2V004XUpTGiuKK3B__djF8DZh6tfdpaqBbDENSFUhac6hHIxyNNoaUIjrVRT82_lUU1ARNTdDUBE0JpkZoY-Tu9Hswe2z-AydixR8xxmwo</recordid><startdate>20010601</startdate><enddate>20010601</enddate><creator>Hikono, H</creator><creator>Ohta, M</creator><creator>Zhou, J H</creator><creator>Sakurai, M</creator><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>20010601</creationdate><title>Expression and distribution of the Kit receptor in bovine bone marrow cells</title><author>Hikono, H ; Ohta, M ; Zhou, J H ; Sakurai, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c295t-4aea866c781e00b2e9da4725a4be6f7c31b9eff9240b0d7ceea87fafa3965bc63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Bone Marrow Cells - metabolism</topic><topic>Cattle - metabolism</topic><topic>Cattle - physiology</topic><topic>Flow Cytometry - veterinary</topic><topic>Granulocyte Colony-Stimulating Factor - physiology</topic><topic>Male</topic><topic>Proto-Oncogene Proteins c-kit - biosynthesis</topic><topic>Proto-Oncogene Proteins c-kit - metabolism</topic><topic>Stem Cell Factor - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hikono, H</creatorcontrib><creatorcontrib>Ohta, M</creatorcontrib><creatorcontrib>Zhou, J H</creatorcontrib><creatorcontrib>Sakurai, M</creatorcontrib><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>American journal of veterinary research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hikono, H</au><au>Ohta, M</au><au>Zhou, J H</au><au>Sakurai, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression and distribution of the Kit receptor in bovine bone marrow cells</atitle><jtitle>American journal of veterinary research</jtitle><addtitle>Am J Vet Res</addtitle><date>2001-06-01</date><risdate>2001</risdate><volume>62</volume><issue>6</issue><spage>974</spage><epage>977</epage><pages>974-977</pages><issn>0002-9645</issn><abstract>To characterize the expression and distribution of the Kit receptor in bovine bone marrow cells (BMC) and to define the function of its ligand, stem cell factor (SCF). Six 7- to 70-day-old healthy male Holstein-Friesian calves. Expression and distribution of the Kit receptor were assessed by use of flow cytometry with monoclonal antibodies (mAb) against the bovine Kit protein. Using Giemsa-stained centrifuged preparations, the histologic appearance of Kit receptor positive (Kit+) BMC were evaluated. Semisolid cultures supplemented with granulocyte colony-stimulating factor (G-CSF) and SCF were used to measure the colony formation capacity of Kit+ BMC. The Kit receptor was expressed on approximately 18% of total BMC. Most of Kit+ BMC did not coexpress lineage markers, but a small subset of this population did coexpress CD3. The Kit+CD3- BMC were a heterogeneous cell population comprising blast-like cells such as myeloblasts, promyelocytes, rubriblasts, and prorubricytes. Conversely, Kit+CD3+ BMC had a lymphocyte-like appearance. Kit+ BMC formed colonies in semisolid culture with G-CSF, whereas Kit- BMC failed to grow. Addition of SCF to G-CSF resulted in superadditive enhancement in colony numbers and size. The Kit receptor is expressed primarily on immature blood cells in bovine bone marrow, and Kit+ BMC contain hematopoietic progenitor cells that are reactive to G-CSF. In addition, SCF synergizes with G-CSF to stimulate colony formation by these cells. Our results suggest that the Kit receptor and its ligand, SCF, are involved in early stages of granulopoiesis in calves.</abstract><cop>United States</cop><pmid>11400859</pmid><doi>10.2460/ajvr.2001.62.974</doi><tpages>4</tpages></addata></record>
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subjects Animals
Bone Marrow Cells - metabolism
Cattle - metabolism
Cattle - physiology
Flow Cytometry - veterinary
Granulocyte Colony-Stimulating Factor - physiology
Male
Proto-Oncogene Proteins c-kit - biosynthesis
Proto-Oncogene Proteins c-kit - metabolism
Stem Cell Factor - physiology
title Expression and distribution of the Kit receptor in bovine bone marrow cells
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