Dermatan sulfotransferase Chst14/D4st1, but not chondroitin sulfotransferase Chst11/C4st1, regulates proliferation and neurogenesis of neural progenitor cells.

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Dermatan sulfotransferase Chst14/D4st1, but not chondroitin sulfotransferase Chst11/C4st1, regulates proliferation and neurogenesis of neural progenitor cells. / Bian, Shan; Akyüz, Nuray; Bernreuther, Christian; Loers, Gabriele; Laczynska, Ewa; Jakovcevski, Igor; Schachner, Melitta.

in: J CELL SCI, Jahrgang 124, Nr. Pt 23, Pt 23, 2011, S. 4051-4063.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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@article{0ca8641b2ad34ae780fe16008ac11a69,
title = "Dermatan sulfotransferase Chst14/D4st1, but not chondroitin sulfotransferase Chst11/C4st1, regulates proliferation and neurogenesis of neural progenitor cells.",
abstract = "Chondroitin sulfates (CSs) and dermatan sulfates (DSs) are enriched in the microenvironment of neural stem cells (NSCs) during development and in the adult neurogenic niche, and have been implicated in mechanisms governing neural precursor migration, proliferation and differentiation. In contrast to previous studies, in which a chondroitinaseABC-dependent unselective deglycosylation of both CSs and DSs was performed, we used chondroitin 4-O-sulfotransferase-1 (Chst11/C4st1)- and dermatan 4-O-sulfotransferase-1 (Chst14/D4st1)-deficient NSCs specific for CSs and DSs, respectively, to investigate the involvement of specific sulfation profiles of CS and DS chains, and thus the potentially distinct roles of CSs and DSs in NSC biology. In comparison to wild-type controls, deficiency for Chst14 resulted in decreased neurogenesis and diminished proliferation of NSCs accompanied by increased expression of GLAST and decreased expression of Mash-1, and an upregulation of the expression of the receptors for fibroblast growth factor-2 (FGF-2) and epidermal growth factor (EGF). By contrast, deficiency in Chst11 did not influence NSC proliferation, migration or differentiation. These observations indicate for the first time that CSs and DSs play distinct roles in the self-renewal and differentiation of NSCs.",
keywords = "Animals, Immunohistochemistry, Mice, Mice, Inbred C57BL, Cell Movement, Apoptosis, Cell Differentiation, *Cell Proliferation, Basic Helix-Loop-Helix Transcription Factors/genetics/metabolism, Bromodeoxyuridine/administration & dosage/pharmacology, Embryo, Mammalian/cytology/drug effects/metabolism, Excitatory Amino Acid Transporter 1/genetics/metabolism, Gene Expression Regulation, Enzymologic, Neural Stem Cells/cytology/drug effects/*enzymology, Neurogenesis, Receptor, Epidermal Growth Factor/genetics/metabolism, Receptor, Fibroblast Growth Factor, Type 2/genetics/metabolism, Stem Cell Niche, Sulfotransferases/genetics/*metabolism, Animals, Immunohistochemistry, Mice, Mice, Inbred C57BL, Cell Movement, Apoptosis, Cell Differentiation, *Cell Proliferation, Basic Helix-Loop-Helix Transcription Factors/genetics/metabolism, Bromodeoxyuridine/administration & dosage/pharmacology, Embryo, Mammalian/cytology/drug effects/metabolism, Excitatory Amino Acid Transporter 1/genetics/metabolism, Gene Expression Regulation, Enzymologic, Neural Stem Cells/cytology/drug effects/*enzymology, Neurogenesis, Receptor, Epidermal Growth Factor/genetics/metabolism, Receptor, Fibroblast Growth Factor, Type 2/genetics/metabolism, Stem Cell Niche, Sulfotransferases/genetics/*metabolism",
author = "Shan Bian and Nuray Aky{\"u}z and Christian Bernreuther and Gabriele Loers and Ewa Laczynska and Igor Jakovcevski and Melitta Schachner",
year = "2011",
language = "English",
volume = "124",
pages = "4051--4063",
journal = "J CELL SCI",
issn = "0021-9533",
publisher = "Company of Biologists Ltd",
number = "Pt 23",

}

RIS

TY - JOUR

T1 - Dermatan sulfotransferase Chst14/D4st1, but not chondroitin sulfotransferase Chst11/C4st1, regulates proliferation and neurogenesis of neural progenitor cells.

AU - Bian, Shan

AU - Akyüz, Nuray

AU - Bernreuther, Christian

AU - Loers, Gabriele

AU - Laczynska, Ewa

AU - Jakovcevski, Igor

AU - Schachner, Melitta

PY - 2011

Y1 - 2011

N2 - Chondroitin sulfates (CSs) and dermatan sulfates (DSs) are enriched in the microenvironment of neural stem cells (NSCs) during development and in the adult neurogenic niche, and have been implicated in mechanisms governing neural precursor migration, proliferation and differentiation. In contrast to previous studies, in which a chondroitinaseABC-dependent unselective deglycosylation of both CSs and DSs was performed, we used chondroitin 4-O-sulfotransferase-1 (Chst11/C4st1)- and dermatan 4-O-sulfotransferase-1 (Chst14/D4st1)-deficient NSCs specific for CSs and DSs, respectively, to investigate the involvement of specific sulfation profiles of CS and DS chains, and thus the potentially distinct roles of CSs and DSs in NSC biology. In comparison to wild-type controls, deficiency for Chst14 resulted in decreased neurogenesis and diminished proliferation of NSCs accompanied by increased expression of GLAST and decreased expression of Mash-1, and an upregulation of the expression of the receptors for fibroblast growth factor-2 (FGF-2) and epidermal growth factor (EGF). By contrast, deficiency in Chst11 did not influence NSC proliferation, migration or differentiation. These observations indicate for the first time that CSs and DSs play distinct roles in the self-renewal and differentiation of NSCs.

AB - Chondroitin sulfates (CSs) and dermatan sulfates (DSs) are enriched in the microenvironment of neural stem cells (NSCs) during development and in the adult neurogenic niche, and have been implicated in mechanisms governing neural precursor migration, proliferation and differentiation. In contrast to previous studies, in which a chondroitinaseABC-dependent unselective deglycosylation of both CSs and DSs was performed, we used chondroitin 4-O-sulfotransferase-1 (Chst11/C4st1)- and dermatan 4-O-sulfotransferase-1 (Chst14/D4st1)-deficient NSCs specific for CSs and DSs, respectively, to investigate the involvement of specific sulfation profiles of CS and DS chains, and thus the potentially distinct roles of CSs and DSs in NSC biology. In comparison to wild-type controls, deficiency for Chst14 resulted in decreased neurogenesis and diminished proliferation of NSCs accompanied by increased expression of GLAST and decreased expression of Mash-1, and an upregulation of the expression of the receptors for fibroblast growth factor-2 (FGF-2) and epidermal growth factor (EGF). By contrast, deficiency in Chst11 did not influence NSC proliferation, migration or differentiation. These observations indicate for the first time that CSs and DSs play distinct roles in the self-renewal and differentiation of NSCs.

KW - Animals

KW - Immunohistochemistry

KW - Mice

KW - Mice, Inbred C57BL

KW - Cell Movement

KW - Apoptosis

KW - Cell Differentiation

KW - Cell Proliferation

KW - Basic Helix-Loop-Helix Transcription Factors/genetics/metabolism

KW - Bromodeoxyuridine/administration & dosage/pharmacology

KW - Embryo, Mammalian/cytology/drug effects/metabolism

KW - Excitatory Amino Acid Transporter 1/genetics/metabolism

KW - Gene Expression Regulation, Enzymologic

KW - Neural Stem Cells/cytology/drug effects/enzymology

KW - Neurogenesis

KW - Receptor, Epidermal Growth Factor/genetics/metabolism

KW - Receptor, Fibroblast Growth Factor, Type 2/genetics/metabolism

KW - Stem Cell Niche

KW - Sulfotransferases/genetics/metabolism

KW - Animals

KW - Immunohistochemistry

KW - Mice

KW - Mice, Inbred C57BL

KW - Cell Movement

KW - Apoptosis

KW - Cell Differentiation

KW - Cell Proliferation

KW - Basic Helix-Loop-Helix Transcription Factors/genetics/metabolism

KW - Bromodeoxyuridine/administration & dosage/pharmacology

KW - Embryo, Mammalian/cytology/drug effects/metabolism

KW - Excitatory Amino Acid Transporter 1/genetics/metabolism

KW - Gene Expression Regulation, Enzymologic

KW - Neural Stem Cells/cytology/drug effects/enzymology

KW - Neurogenesis

KW - Receptor, Epidermal Growth Factor/genetics/metabolism

KW - Receptor, Fibroblast Growth Factor, Type 2/genetics/metabolism

KW - Stem Cell Niche

KW - Sulfotransferases/genetics/metabolism

M3 - SCORING: Journal article

VL - 124

SP - 4051

EP - 4063

JO - J CELL SCI

JF - J CELL SCI

SN - 0021-9533

IS - Pt 23

M1 - Pt 23

ER -