Folliculo-stellate cells of the human pituitary: A type of adult stem cell?
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Horvath, E
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Univ Toronto, St Michaels Hosp, Dept Lab Med & Pathobiol, Toronto, ON M5B 1W8, CanadaUniv Toronto, St Michaels Hosp, Dept Lab Med & Pathobiol, Toronto, ON M5B 1W8, Canada
Horvath, E
[1
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Kovacs, K
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Univ Toronto, St Michaels Hosp, Dept Lab Med & Pathobiol, Toronto, ON M5B 1W8, CanadaUniv Toronto, St Michaels Hosp, Dept Lab Med & Pathobiol, Toronto, ON M5B 1W8, Canada
Kovacs, K
[1
]
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[1] Univ Toronto, St Michaels Hosp, Dept Lab Med & Pathobiol, Toronto, ON M5B 1W8, Canada
Ultrastructural and immunocytochemical observations of pituitary folliculo-stellate cells (FSC) in a large series of adenomatous and nontumorous human pituitaries led to the following conclusions: (1) The endocrine cells of both the nontumorous and the adenomatous pituitary are capable of transforming into FSC while changing from endocrine to nonendocrine phenotype. (2) As shown on consecutive sections in prolactin cell adenomas with FSC-rich areas including microcyst formation, S-100 protein and glial fibrillary acidic protein (GFAP) immunoreactivities are strongest in the smallest newly formed follicles. The 2 immunoreactivities do not overlap. The epithelium of older microcysts is immunonegative, implying that expression of the 2 markers is restricted to the early phase of FSC formation. (3) Transformation of endocrine cells into FSC may signify retrodifferentiation into their Rathke's pouch derived precursors as suggested by occasional presence of ciliated and/or mucin producing cells in the lining of microcysts. (4) In lymphocytic hypophysitis a marked activation as well as increase of number and size of FSC are evident in areas of ongoing immune destruction supporting their immune role. (5) Considering the multifaceted nature of FSC, it is suggested that they represent a type of pluripotent adult stem cell.
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Univ Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, GermanyUniv Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, Germany
Botermann, Dominik Simon
Brandes, Nadine
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Univ Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, GermanyUniv Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, Germany
Brandes, Nadine
Frommhold, Anke
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Univ Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, GermanyUniv Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, Germany
Frommhold, Anke
Hess, Ina
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Univ Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, GermanyUniv Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, Germany
Hess, Ina
Wolff, Alexander
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Univ Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, GermanyUniv Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, Germany
Wolff, Alexander
Zibat, Arne
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Univ Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, GermanyUniv Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, Germany
Zibat, Arne
Hahn, Heidi
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Univ Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, GermanyUniv Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, Germany
Hahn, Heidi
Buslei, Rolf
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Klinikum Bruderwald, Inst Pathol, Sozialstiftung Bamberg, Bamberg, GermanyUniv Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, Germany
Buslei, Rolf
Uhmann, Anja
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Univ Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, GermanyUniv Med Ctr, Inst Human Genet, Mol Dev Genet & Tumor Genet Grp, Gottingen, Germany