Hyaluronate and its receptors in bone marrow.

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Hyaluronate and its receptors in bone marrow. / Schade, Ulrika M; Nehmann, Nina; Horny, Hans-P; Prehm, Peter; Delpech, Bertrand; Krüger, William H; Zander, Axel R.; Schumacher, Udo.

In: ACTA HISTOCHEM, Vol. 108, No. 2, 2, 2006, p. 141-147.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Schade, UM, Nehmann, N, Horny, H-P, Prehm, P, Delpech, B, Krüger, WH, Zander, AR & Schumacher, U 2006, 'Hyaluronate and its receptors in bone marrow.', ACTA HISTOCHEM, vol. 108, no. 2, 2, pp. 141-147. <http://www.ncbi.nlm.nih.gov/pubmed/16713618?dopt=Citation>

APA

Schade, U. M., Nehmann, N., Horny, H-P., Prehm, P., Delpech, B., Krüger, W. H., Zander, A. R., & Schumacher, U. (2006). Hyaluronate and its receptors in bone marrow. ACTA HISTOCHEM, 108(2), 141-147. [2]. http://www.ncbi.nlm.nih.gov/pubmed/16713618?dopt=Citation

Vancouver

Schade UM, Nehmann N, Horny H-P, Prehm P, Delpech B, Krüger WH et al. Hyaluronate and its receptors in bone marrow. ACTA HISTOCHEM. 2006;108(2):141-147. 2.

Bibtex

@article{50c029620bd74c5e8929785fc79817f4,
title = "Hyaluronate and its receptors in bone marrow.",
abstract = "Cell-cell and cell-matrix interactions, which are mediated by cell adhesion molecules, play a fundamental role during many cellular processes including growth, differentiation, cell migration and cancer metastasis. One molecule playing a major role in these processes is the CD44 surface receptor, which is expressed in a wide range of cells including many cells of the hemopoietic system, where it mediates the interaction with its major ligand, hyaluronate. However, little is known about CD44 and hyaluronate in bone marrow and this was investigated immunohistochemically in trephine biopsies and in cultivated human bone marrow stromal cells. In biopsy specimens, patches of hyaluronate deposition were detected in the extracellular matrix (ECM). However, most of the areas of the ECM were devoid of hyaluronate. Single mast cells and lymphocytes scattered throughout the marrow were CD44 immunopositive. Marrow-derived stromal cells (MDSC) expanded in cell culture were immunopositive for CD44, hyaluronate synthase, and hyaluronate. Hence, a marked difference between CD44 immunolocalisation and hyaluronate deposition can be observed between in situ and under cell culture conditions. Since in normal marrow in situ the number of CD44 immunopositive cells was low, interactions of CD44 and hyaluronate would appear to not to play a major role in cell adhesion in the normal bone marrow.",
author = "Schade, {Ulrika M} and Nina Nehmann and Hans-P Horny and Peter Prehm and Bertrand Delpech and Kr{\"u}ger, {William H} and Zander, {Axel R.} and Udo Schumacher",
year = "2006",
language = "Deutsch",
volume = "108",
pages = "141--147",
journal = "ACTA HISTOCHEM",
issn = "0065-1281",
publisher = "Urban und Fischer Verlag Jena",
number = "2",

}

RIS

TY - JOUR

T1 - Hyaluronate and its receptors in bone marrow.

AU - Schade, Ulrika M

AU - Nehmann, Nina

AU - Horny, Hans-P

AU - Prehm, Peter

AU - Delpech, Bertrand

AU - Krüger, William H

AU - Zander, Axel R.

AU - Schumacher, Udo

PY - 2006

Y1 - 2006

N2 - Cell-cell and cell-matrix interactions, which are mediated by cell adhesion molecules, play a fundamental role during many cellular processes including growth, differentiation, cell migration and cancer metastasis. One molecule playing a major role in these processes is the CD44 surface receptor, which is expressed in a wide range of cells including many cells of the hemopoietic system, where it mediates the interaction with its major ligand, hyaluronate. However, little is known about CD44 and hyaluronate in bone marrow and this was investigated immunohistochemically in trephine biopsies and in cultivated human bone marrow stromal cells. In biopsy specimens, patches of hyaluronate deposition were detected in the extracellular matrix (ECM). However, most of the areas of the ECM were devoid of hyaluronate. Single mast cells and lymphocytes scattered throughout the marrow were CD44 immunopositive. Marrow-derived stromal cells (MDSC) expanded in cell culture were immunopositive for CD44, hyaluronate synthase, and hyaluronate. Hence, a marked difference between CD44 immunolocalisation and hyaluronate deposition can be observed between in situ and under cell culture conditions. Since in normal marrow in situ the number of CD44 immunopositive cells was low, interactions of CD44 and hyaluronate would appear to not to play a major role in cell adhesion in the normal bone marrow.

AB - Cell-cell and cell-matrix interactions, which are mediated by cell adhesion molecules, play a fundamental role during many cellular processes including growth, differentiation, cell migration and cancer metastasis. One molecule playing a major role in these processes is the CD44 surface receptor, which is expressed in a wide range of cells including many cells of the hemopoietic system, where it mediates the interaction with its major ligand, hyaluronate. However, little is known about CD44 and hyaluronate in bone marrow and this was investigated immunohistochemically in trephine biopsies and in cultivated human bone marrow stromal cells. In biopsy specimens, patches of hyaluronate deposition were detected in the extracellular matrix (ECM). However, most of the areas of the ECM were devoid of hyaluronate. Single mast cells and lymphocytes scattered throughout the marrow were CD44 immunopositive. Marrow-derived stromal cells (MDSC) expanded in cell culture were immunopositive for CD44, hyaluronate synthase, and hyaluronate. Hence, a marked difference between CD44 immunolocalisation and hyaluronate deposition can be observed between in situ and under cell culture conditions. Since in normal marrow in situ the number of CD44 immunopositive cells was low, interactions of CD44 and hyaluronate would appear to not to play a major role in cell adhesion in the normal bone marrow.

M3 - SCORING: Zeitschriftenaufsatz

VL - 108

SP - 141

EP - 147

JO - ACTA HISTOCHEM

JF - ACTA HISTOCHEM

SN - 0065-1281

IS - 2

M1 - 2

ER -