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Lectin histochemistry of microvascular endothelium in chick and quail musculature.

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Lectin histochemistry of microvascular endothelium in chick and quail musculature. / Nanka, O; Peumans, W J; Van Damme, E J; Pfüller, U; Valásek, P; Halata, Zdenek; Schumacher, U; Grim, M.

In: ANAT EMBRYOL, Vol. 204, No. 5, 5, 2001, p. 407-411.

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Harvard

Nanka, O, Peumans, WJ, Van Damme, EJ, Pfüller, U, Valásek, P, Halata, Z, Schumacher, U & Grim, M 2001, 'Lectin histochemistry of microvascular endothelium in chick and quail musculature.', ANAT EMBRYOL, vol. 204, no. 5, 5, pp. 407-411. <http://www.ncbi.nlm.nih.gov/pubmed/11789988?dopt=Citation>

APA

Nanka, O., Peumans, W. J., Van Damme, E. J., Pfüller, U., Valásek, P., Halata, Z., Schumacher, U., & Grim, M. (2001). Lectin histochemistry of microvascular endothelium in chick and quail musculature. ANAT EMBRYOL, 204(5), 407-411. [5]. http://www.ncbi.nlm.nih.gov/pubmed/11789988?dopt=Citation

Vancouver

Nanka O, Peumans WJ, Van Damme EJ, Pfüller U, Valásek P, Halata Z et al. Lectin histochemistry of microvascular endothelium in chick and quail musculature. ANAT EMBRYOL. 2001;204(5):407-411. 5.

Bibtex

@article{234b1c9439cc401cb6cc1bcea97f75d1,
title = "Lectin histochemistry of microvascular endothelium in chick and quail musculature.",
abstract = "The lectin binding pattern of muscular microvessels in chick, quail and chick/quail chimeras was analysed. Paraffin wax sections of muscles from embryonic and adult animals were used. The biotin-labelled lectins were detected by avidin-alkaline phosphatase complex. The following lectins bound to muscular microvessels including arterioles, capillaries and venules of both species: SNA-I (Sambucus nigra agglutinin), MAA (Maackia amurensis agglutinin), AIA (Artocarpus integrifolia agglutinin), VAA-I, VAA-II and VAA-III (Viscum album agglutinin I-III), WGA (wheat germ agglutinin), LEA (Lycopersicon esculentum agglutinin). Endomysium and basement membranes of muscle fibres were also stained to a variable extent and intensity. Only SNA-I stained almost exclusively the endothelium of blood vessels. WFA (Wisteria floribunda agglutinin) bound to the quail endothelium only. MPA (Maclura pomifera agglutinin) marked vessels in adult muscles of chick and quail, but embryonic vessels were stained in quail only. Our results show that lectin histochemistry is a useful tool for visualisation of microvasculature in avian species. In particular, WFA and MPA can be used to determine the origin of endothelia in chick/quail chimeras.",
author = "O Nanka and Peumans, {W J} and {Van Damme}, {E J} and U Pf{\"u}ller and P Val{\'a}sek and Zdenek Halata and U Schumacher and M Grim",
year = "2001",
language = "Deutsch",
volume = "204",
pages = "407--411",
number = "5",

}

RIS

TY - JOUR

T1 - Lectin histochemistry of microvascular endothelium in chick and quail musculature.

AU - Nanka, O

AU - Peumans, W J

AU - Van Damme, E J

AU - Pfüller, U

AU - Valásek, P

AU - Halata, Zdenek

AU - Schumacher, U

AU - Grim, M

PY - 2001

Y1 - 2001

N2 - The lectin binding pattern of muscular microvessels in chick, quail and chick/quail chimeras was analysed. Paraffin wax sections of muscles from embryonic and adult animals were used. The biotin-labelled lectins were detected by avidin-alkaline phosphatase complex. The following lectins bound to muscular microvessels including arterioles, capillaries and venules of both species: SNA-I (Sambucus nigra agglutinin), MAA (Maackia amurensis agglutinin), AIA (Artocarpus integrifolia agglutinin), VAA-I, VAA-II and VAA-III (Viscum album agglutinin I-III), WGA (wheat germ agglutinin), LEA (Lycopersicon esculentum agglutinin). Endomysium and basement membranes of muscle fibres were also stained to a variable extent and intensity. Only SNA-I stained almost exclusively the endothelium of blood vessels. WFA (Wisteria floribunda agglutinin) bound to the quail endothelium only. MPA (Maclura pomifera agglutinin) marked vessels in adult muscles of chick and quail, but embryonic vessels were stained in quail only. Our results show that lectin histochemistry is a useful tool for visualisation of microvasculature in avian species. In particular, WFA and MPA can be used to determine the origin of endothelia in chick/quail chimeras.

AB - The lectin binding pattern of muscular microvessels in chick, quail and chick/quail chimeras was analysed. Paraffin wax sections of muscles from embryonic and adult animals were used. The biotin-labelled lectins were detected by avidin-alkaline phosphatase complex. The following lectins bound to muscular microvessels including arterioles, capillaries and venules of both species: SNA-I (Sambucus nigra agglutinin), MAA (Maackia amurensis agglutinin), AIA (Artocarpus integrifolia agglutinin), VAA-I, VAA-II and VAA-III (Viscum album agglutinin I-III), WGA (wheat germ agglutinin), LEA (Lycopersicon esculentum agglutinin). Endomysium and basement membranes of muscle fibres were also stained to a variable extent and intensity. Only SNA-I stained almost exclusively the endothelium of blood vessels. WFA (Wisteria floribunda agglutinin) bound to the quail endothelium only. MPA (Maclura pomifera agglutinin) marked vessels in adult muscles of chick and quail, but embryonic vessels were stained in quail only. Our results show that lectin histochemistry is a useful tool for visualisation of microvasculature in avian species. In particular, WFA and MPA can be used to determine the origin of endothelia in chick/quail chimeras.

M3 - SCORING: Zeitschriftenaufsatz

VL - 204

SP - 407

EP - 411

IS - 5

M1 - 5

ER -