Histo- and cytophysiology of the lactating mammary gland of the African elephant (Loxodonta africana)
The lactating mammary gland of the African elephant (Loxodonta africana) has been studied with a panel of morphological techniques focusing on (1) the functional changes during the secretory process, (2) proliferative process [by application of proliferating cell nuclear antigen (PCNA) immunohistoch...
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Veröffentlicht in: | Cell and tissue research 1998-12, Vol.294 (3), p.485-501 |
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description | The lactating mammary gland of the African elephant (Loxodonta africana) has been studied with a panel of morphological techniques focusing on (1) the functional changes during the secretory process, (2) proliferative process [by application of proliferating cell nuclear antigen (PCNA) immunohistochemistry] and apoptotic phenomena [by use of the TUNEL technique] in the individual lobules, and (3) components of milk and milk-fat-globule membrane. In the lactating gland, the lobules are variably differentiated; within a lobule, however, the alveoli are usually similarly differentiated. The morphology of their alveoli suggests a classification of the lobules into types 1-3. Lobules of type 1 are composed of immature tubular alveoli with mitotic figures and numerous PCNA-positive nuclei; advanced type 1 alveoli contain abundant glycogen and specific secretory granules. Lobules of type 2 are further subdivided. In type 2a lobules, the epithelial cells of the alveoli form tall apical protrusions, which in part are occupied by small lipid droplets and which are pinched off in an apocrine fashion. The number of lysosomes varies considerably. Type 2b is the most common type, with striking basal membrane foldings, abundant rough endoplasmic reticulum cisterns, large Golgi apparatus, numerous mitochondria, lipid droplets, and protein vesicles with 30- to 90-nm-wide casein micelles. The lipid droplets are pinched off with minimal amounts of cytoplasm. Type 2c is composed of alveoli with a cuboidal epithelium and few signs of secretory activity. Increasing expression of peanut-agglutinin-binding sites parallels the maturation and differentiation of the glandular cells. Type 3 lobules are marked by numerous TUNEL-positive nuclei and large lipid droplets and are apparently degenerating structures. Cytokeratin (CK) 14 is usually present in the myoepithelial cells; CK 19 and CK 7 mark ductal and immature alveolar epithelia. Milk protein content varies between 2.6% and 6.3%, and casein micelles range from 35 to 90 nm in diameter. The diameter of intra-alveolar milk fat globules ranges from 5 to 25 micrometer and the membranes bear a filamentous surface coat composed of membrane-anchored mucins; gel-electrophoretic analysis of these mucins from different individuals demonstrates the presence of mucin MUC 1, which is expressed with considerable genetic heterogeneity. |
doi_str_mv | 10.1007/s004410051200 |
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In the lactating gland, the lobules are variably differentiated; within a lobule, however, the alveoli are usually similarly differentiated. The morphology of their alveoli suggests a classification of the lobules into types 1-3. Lobules of type 1 are composed of immature tubular alveoli with mitotic figures and numerous PCNA-positive nuclei; advanced type 1 alveoli contain abundant glycogen and specific secretory granules. Lobules of type 2 are further subdivided. In type 2a lobules, the epithelial cells of the alveoli form tall apical protrusions, which in part are occupied by small lipid droplets and which are pinched off in an apocrine fashion. The number of lysosomes varies considerably. Type 2b is the most common type, with striking basal membrane foldings, abundant rough endoplasmic reticulum cisterns, large Golgi apparatus, numerous mitochondria, lipid droplets, and protein vesicles with 30- to 90-nm-wide casein micelles. The lipid droplets are pinched off with minimal amounts of cytoplasm. Type 2c is composed of alveoli with a cuboidal epithelium and few signs of secretory activity. Increasing expression of peanut-agglutinin-binding sites parallels the maturation and differentiation of the glandular cells. Type 3 lobules are marked by numerous TUNEL-positive nuclei and large lipid droplets and are apparently degenerating structures. Cytokeratin (CK) 14 is usually present in the myoepithelial cells; CK 19 and CK 7 mark ductal and immature alveolar epithelia. Milk protein content varies between 2.6% and 6.3%, and casein micelles range from 35 to 90 nm in diameter. The diameter of intra-alveolar milk fat globules ranges from 5 to 25 micrometer and the membranes bear a filamentous surface coat composed of membrane-anchored mucins; gel-electrophoretic analysis of these mucins from different individuals demonstrates the presence of mucin MUC 1, which is expressed with considerable genetic heterogeneity.</description><identifier>ISSN: 0302-766X</identifier><identifier>EISSN: 1432-0878</identifier><identifier>DOI: 10.1007/s004410051200</identifier><identifier>PMID: 9799466</identifier><language>eng</language><publisher>Germany</publisher><subject>Animals ; Elephants ; Female ; Freeze Etching ; Freeze Fracturing ; Immunohistochemistry ; Lactation - physiology ; Mammary Glands, Animal - cytology ; Mammary Glands, Animal - physiology ; Mammary Glands, Animal - ultrastructure ; Microscopy, Electron ; Milk - cytology ; Nipples - cytology ; Nipples - physiology ; Nipples - ultrastructure</subject><ispartof>Cell and tissue research, 1998-12, Vol.294 (3), p.485-501</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c288t-87a1951599817d702067657c55915f49a7f4a02251bd2878efce9c82fb2970283</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9799466$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Welsch, U</creatorcontrib><creatorcontrib>Feuerhake, F</creatorcontrib><creatorcontrib>van Aarde, R</creatorcontrib><creatorcontrib>Buchheim, W</creatorcontrib><creatorcontrib>Patton, S</creatorcontrib><title>Histo- and cytophysiology of the lactating mammary gland of the African elephant (Loxodonta africana)</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><description>The lactating mammary gland of the African elephant (Loxodonta africana) has been studied with a panel of morphological techniques focusing on (1) the functional changes during the secretory process, (2) proliferative process [by application of proliferating cell nuclear antigen (PCNA) immunohistochemistry] and apoptotic phenomena [by use of the TUNEL technique] in the individual lobules, and (3) components of milk and milk-fat-globule membrane. In the lactating gland, the lobules are variably differentiated; within a lobule, however, the alveoli are usually similarly differentiated. The morphology of their alveoli suggests a classification of the lobules into types 1-3. Lobules of type 1 are composed of immature tubular alveoli with mitotic figures and numerous PCNA-positive nuclei; advanced type 1 alveoli contain abundant glycogen and specific secretory granules. Lobules of type 2 are further subdivided. In type 2a lobules, the epithelial cells of the alveoli form tall apical protrusions, which in part are occupied by small lipid droplets and which are pinched off in an apocrine fashion. The number of lysosomes varies considerably. Type 2b is the most common type, with striking basal membrane foldings, abundant rough endoplasmic reticulum cisterns, large Golgi apparatus, numerous mitochondria, lipid droplets, and protein vesicles with 30- to 90-nm-wide casein micelles. The lipid droplets are pinched off with minimal amounts of cytoplasm. Type 2c is composed of alveoli with a cuboidal epithelium and few signs of secretory activity. Increasing expression of peanut-agglutinin-binding sites parallels the maturation and differentiation of the glandular cells. Type 3 lobules are marked by numerous TUNEL-positive nuclei and large lipid droplets and are apparently degenerating structures. Cytokeratin (CK) 14 is usually present in the myoepithelial cells; CK 19 and CK 7 mark ductal and immature alveolar epithelia. Milk protein content varies between 2.6% and 6.3%, and casein micelles range from 35 to 90 nm in diameter. The diameter of intra-alveolar milk fat globules ranges from 5 to 25 micrometer and the membranes bear a filamentous surface coat composed of membrane-anchored mucins; gel-electrophoretic analysis of these mucins from different individuals demonstrates the presence of mucin MUC 1, which is expressed with considerable genetic heterogeneity.</description><subject>Animals</subject><subject>Elephants</subject><subject>Female</subject><subject>Freeze Etching</subject><subject>Freeze Fracturing</subject><subject>Immunohistochemistry</subject><subject>Lactation - physiology</subject><subject>Mammary Glands, Animal - cytology</subject><subject>Mammary Glands, Animal - physiology</subject><subject>Mammary Glands, Animal - ultrastructure</subject><subject>Microscopy, Electron</subject><subject>Milk - cytology</subject><subject>Nipples - cytology</subject><subject>Nipples - physiology</subject><subject>Nipples - ultrastructure</subject><issn>0302-766X</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkMFLwzAUxoMoc06PHoWcRA_Vl7RpkuMY6oSBFwVvJUuTrdI2tUnB_vdmrAie3gfv9z7e9yF0TeCBAPBHD5BlUTFCAU7QnGQpTUBwcYrmkAJNeJ5_nqML778ASJbncoZmkksZ5RyZdeWDS7BqS6zH4Lr96CtXu92IncVhb3CtdFChane4UU2j-hHv6gM9rZe2r7RqsalNt1dtwHcb9-NK1waF1XGn7i_RmVW1N1fTXKCP56f31TrZvL28rpabRFMhQiK4IpIRJqUgvORAIec545oxSZjNpOI2U0ApI9uSxoTGaiO1oHZLZaRFukC3R9-ud9-D8aFoKq9NHR82bvAFh3idMRLB5Ajq3nnfG1t0fXUIVxAoDrUW_2qN_M1kPGwbU_7RU4_pL1yDcWQ</recordid><startdate>19981201</startdate><enddate>19981201</enddate><creator>Welsch, U</creator><creator>Feuerhake, F</creator><creator>van Aarde, R</creator><creator>Buchheim, W</creator><creator>Patton, S</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>19981201</creationdate><title>Histo- and cytophysiology of the lactating mammary gland of the African elephant (Loxodonta africana)</title><author>Welsch, U ; Feuerhake, F ; van Aarde, R ; Buchheim, W ; Patton, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c288t-87a1951599817d702067657c55915f49a7f4a02251bd2878efce9c82fb2970283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Elephants</topic><topic>Female</topic><topic>Freeze Etching</topic><topic>Freeze Fracturing</topic><topic>Immunohistochemistry</topic><topic>Lactation - physiology</topic><topic>Mammary Glands, Animal - cytology</topic><topic>Mammary Glands, Animal - physiology</topic><topic>Mammary Glands, Animal - ultrastructure</topic><topic>Microscopy, Electron</topic><topic>Milk - cytology</topic><topic>Nipples - cytology</topic><topic>Nipples - physiology</topic><topic>Nipples - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Welsch, U</creatorcontrib><creatorcontrib>Feuerhake, F</creatorcontrib><creatorcontrib>van Aarde, R</creatorcontrib><creatorcontrib>Buchheim, W</creatorcontrib><creatorcontrib>Patton, S</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>Cell and tissue research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Welsch, U</au><au>Feuerhake, F</au><au>van Aarde, R</au><au>Buchheim, W</au><au>Patton, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Histo- and cytophysiology of the lactating mammary gland of the African elephant (Loxodonta africana)</atitle><jtitle>Cell and tissue research</jtitle><addtitle>Cell Tissue Res</addtitle><date>1998-12-01</date><risdate>1998</risdate><volume>294</volume><issue>3</issue><spage>485</spage><epage>501</epage><pages>485-501</pages><issn>0302-766X</issn><eissn>1432-0878</eissn><abstract>The lactating mammary gland of the African elephant (Loxodonta africana) has been studied with a panel of morphological techniques focusing on (1) the functional changes during the secretory process, (2) proliferative process [by application of proliferating cell nuclear antigen (PCNA) immunohistochemistry] and apoptotic phenomena [by use of the TUNEL technique] in the individual lobules, and (3) components of milk and milk-fat-globule membrane. In the lactating gland, the lobules are variably differentiated; within a lobule, however, the alveoli are usually similarly differentiated. The morphology of their alveoli suggests a classification of the lobules into types 1-3. Lobules of type 1 are composed of immature tubular alveoli with mitotic figures and numerous PCNA-positive nuclei; advanced type 1 alveoli contain abundant glycogen and specific secretory granules. Lobules of type 2 are further subdivided. In type 2a lobules, the epithelial cells of the alveoli form tall apical protrusions, which in part are occupied by small lipid droplets and which are pinched off in an apocrine fashion. The number of lysosomes varies considerably. Type 2b is the most common type, with striking basal membrane foldings, abundant rough endoplasmic reticulum cisterns, large Golgi apparatus, numerous mitochondria, lipid droplets, and protein vesicles with 30- to 90-nm-wide casein micelles. The lipid droplets are pinched off with minimal amounts of cytoplasm. Type 2c is composed of alveoli with a cuboidal epithelium and few signs of secretory activity. Increasing expression of peanut-agglutinin-binding sites parallels the maturation and differentiation of the glandular cells. Type 3 lobules are marked by numerous TUNEL-positive nuclei and large lipid droplets and are apparently degenerating structures. Cytokeratin (CK) 14 is usually present in the myoepithelial cells; CK 19 and CK 7 mark ductal and immature alveolar epithelia. Milk protein content varies between 2.6% and 6.3%, and casein micelles range from 35 to 90 nm in diameter. The diameter of intra-alveolar milk fat globules ranges from 5 to 25 micrometer and the membranes bear a filamentous surface coat composed of membrane-anchored mucins; gel-electrophoretic analysis of these mucins from different individuals demonstrates the presence of mucin MUC 1, which is expressed with considerable genetic heterogeneity.</abstract><cop>Germany</cop><pmid>9799466</pmid><doi>10.1007/s004410051200</doi><tpages>17</tpages></addata></record> |
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subjects | Animals Elephants Female Freeze Etching Freeze Fracturing Immunohistochemistry Lactation - physiology Mammary Glands, Animal - cytology Mammary Glands, Animal - physiology Mammary Glands, Animal - ultrastructure Microscopy, Electron Milk - cytology Nipples - cytology Nipples - physiology Nipples - ultrastructure |
title | Histo- and cytophysiology of the lactating mammary gland of the African elephant (Loxodonta africana) |
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