Chondroitin-6-sulfate-containing proteoglycan: a new component of human skin dermoepidermal junction.

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Chondroitin-6-sulfate-containing proteoglycan: a new component of human skin dermoepidermal junction. / Fine, J D; Couchman, J R.

In: Journal of Investigative Dermatology, Vol. 90, No. 3, 1988, p. 283-8.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Fine, JD & Couchman, JR 1988, 'Chondroitin-6-sulfate-containing proteoglycan: a new component of human skin dermoepidermal junction.', Journal of Investigative Dermatology, vol. 90, no. 3, pp. 283-8.

APA

Fine, J. D., & Couchman, J. R. (1988). Chondroitin-6-sulfate-containing proteoglycan: a new component of human skin dermoepidermal junction. Journal of Investigative Dermatology, 90(3), 283-8.

Vancouver

Fine JD, Couchman JR. Chondroitin-6-sulfate-containing proteoglycan: a new component of human skin dermoepidermal junction. Journal of Investigative Dermatology. 1988;90(3):283-8.

Author

Fine, J D ; Couchman, J R. / Chondroitin-6-sulfate-containing proteoglycan: a new component of human skin dermoepidermal junction. In: Journal of Investigative Dermatology. 1988 ; Vol. 90, No. 3. pp. 283-8.

Bibtex

@article{73aa4770598311dd8d9f000ea68e967b,
title = "Chondroitin-6-sulfate-containing proteoglycan: a new component of human skin dermoepidermal junction.",
abstract = "A murine monoclonal antibody (3B3) has been produced with specificity for chondroitin-6-sulfate (C-6-S) and proven binding to rodent basement membranes, presumably detecting a population of C-6-S-containing proteoglycans. Utilizing this antibody, we sought to determine whether a basement membrane chondroitin sulfate proteoglycan is present in adult, neonatal, and/or fetal skin, and if present, its ultrastructural localization. Indirect immunofluorescence was performed on human adult, neonatal, and fetal skin. To detect the antigen, specimens were pretreated with chondroitinase ABC; absence of enzyme treatment served as negative control. Chondroitin sulfate proteoglycan was detectable in linear homogeneous array along the dermoepidermal junction and within vascular (and when present, adnexal) basement membranes in both adult and neonatal skin. In fetal skin, basement membrane staining was noted as early as 54 gestational days. Indirect immunoelectron microscopy and NaCl-split skin studies were performed to ultrastructurally localize the antigen; immune deposits were detectable within the lamina densa in chondroitinase-treated skin. These findings demonstrate that chondroitin sulfate proteoglycan is present within all skin basement membranes; that it is present in the region of the lamina densa; and that similar to some other ubiquitous basement membrane antigens, it is present early in the developing fetus.",
author = "Fine, {J D} and Couchman, {J R}",
note = "Keywords: Adult; Antibodies, Monoclonal; Epidermis; Fetus; Fluorescent Antibody Technique; Humans; Proteochondroitin Sulfates; Proteoglycans; Skin",
year = "1988",
language = "English",
volume = "90",
pages = "283--8",
journal = "Journal of Investigative Dermatology",
issn = "0022-202X",
publisher = "nature publishing group",
number = "3",

}

RIS

TY - JOUR

T1 - Chondroitin-6-sulfate-containing proteoglycan: a new component of human skin dermoepidermal junction.

AU - Fine, J D

AU - Couchman, J R

N1 - Keywords: Adult; Antibodies, Monoclonal; Epidermis; Fetus; Fluorescent Antibody Technique; Humans; Proteochondroitin Sulfates; Proteoglycans; Skin

PY - 1988

Y1 - 1988

N2 - A murine monoclonal antibody (3B3) has been produced with specificity for chondroitin-6-sulfate (C-6-S) and proven binding to rodent basement membranes, presumably detecting a population of C-6-S-containing proteoglycans. Utilizing this antibody, we sought to determine whether a basement membrane chondroitin sulfate proteoglycan is present in adult, neonatal, and/or fetal skin, and if present, its ultrastructural localization. Indirect immunofluorescence was performed on human adult, neonatal, and fetal skin. To detect the antigen, specimens were pretreated with chondroitinase ABC; absence of enzyme treatment served as negative control. Chondroitin sulfate proteoglycan was detectable in linear homogeneous array along the dermoepidermal junction and within vascular (and when present, adnexal) basement membranes in both adult and neonatal skin. In fetal skin, basement membrane staining was noted as early as 54 gestational days. Indirect immunoelectron microscopy and NaCl-split skin studies were performed to ultrastructurally localize the antigen; immune deposits were detectable within the lamina densa in chondroitinase-treated skin. These findings demonstrate that chondroitin sulfate proteoglycan is present within all skin basement membranes; that it is present in the region of the lamina densa; and that similar to some other ubiquitous basement membrane antigens, it is present early in the developing fetus.

AB - A murine monoclonal antibody (3B3) has been produced with specificity for chondroitin-6-sulfate (C-6-S) and proven binding to rodent basement membranes, presumably detecting a population of C-6-S-containing proteoglycans. Utilizing this antibody, we sought to determine whether a basement membrane chondroitin sulfate proteoglycan is present in adult, neonatal, and/or fetal skin, and if present, its ultrastructural localization. Indirect immunofluorescence was performed on human adult, neonatal, and fetal skin. To detect the antigen, specimens were pretreated with chondroitinase ABC; absence of enzyme treatment served as negative control. Chondroitin sulfate proteoglycan was detectable in linear homogeneous array along the dermoepidermal junction and within vascular (and when present, adnexal) basement membranes in both adult and neonatal skin. In fetal skin, basement membrane staining was noted as early as 54 gestational days. Indirect immunoelectron microscopy and NaCl-split skin studies were performed to ultrastructurally localize the antigen; immune deposits were detectable within the lamina densa in chondroitinase-treated skin. These findings demonstrate that chondroitin sulfate proteoglycan is present within all skin basement membranes; that it is present in the region of the lamina densa; and that similar to some other ubiquitous basement membrane antigens, it is present early in the developing fetus.

M3 - Journal article

C2 - 3279132

VL - 90

SP - 283

EP - 288

JO - Journal of Investigative Dermatology

JF - Journal of Investigative Dermatology

SN - 0022-202X

IS - 3

ER -

ID: 5167398