Basement membrane proteoglycans and development.

Research output: Contribution to journalJournal articleResearchpeer-review

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Basement membrane proteoglycans and development. / Couchman, J R; Abrahamson, D R; McCarthy, K J.

In: Kidney International, Vol. 43, No. 1, 1993, p. 79-84.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Couchman, JR, Abrahamson, DR & McCarthy, KJ 1993, 'Basement membrane proteoglycans and development.', Kidney International, vol. 43, no. 1, pp. 79-84.

APA

Couchman, J. R., Abrahamson, D. R., & McCarthy, K. J. (1993). Basement membrane proteoglycans and development. Kidney International, 43(1), 79-84.

Vancouver

Couchman JR, Abrahamson DR, McCarthy KJ. Basement membrane proteoglycans and development. Kidney International. 1993;43(1):79-84.

Author

Couchman, J R ; Abrahamson, D R ; McCarthy, K J. / Basement membrane proteoglycans and development. In: Kidney International. 1993 ; Vol. 43, No. 1. pp. 79-84.

Bibtex

@article{37ca7ed0597b11dd8d9f000ea68e967b,
title = "Basement membrane proteoglycans and development.",
abstract = "Basement membranes contain distinct collagen, glycoprotein and proteoglycan species, and these exhibit considerable heterogeneity in isoform or type when different tissue types are compared. Additionally, many components are differentially expressed in organogenesis. We have considered the distributions in glomerulogenesis of two distinct basement membrane proteoglycans, a small heparan sulfate proteoglycan and a chondroitin sulfate proteoglycan (BM-CSPG). While the former was present in all kidney basement membranes through development, the latter was apparently regulated in distribution. BM-CSPG was only strongly expressed in the vasculature invading late comma stage glomeruli, and later in presumptive and mature Bowman's capsule. Over the first six to eight weeks, the capillary basement membranes contained BM-CSPG, but in gradually decreasing amounts until it became completely undetectable. The basement membrane of the adult rat glomerulus is unique in its lack of BM-CSPG. However, in diabetic rats, BM-CSPG is apparently re-expressed in the glomerular basement membrane, a potential marker for pathological changes in glomerular structure. While its function awaits elucidation, BM-CSPG may be essential for basement membrane integrity or stability and have important roles in kidney development.",
author = "Couchman, {J R} and Abrahamson, {D R} and McCarthy, {K J}",
note = "Keywords: Animals; Basement Membrane; Diabetes Mellitus, Experimental; Heparan Sulfate Proteoglycans; Heparitin Sulfate; Kidney; Microscopy, Immunoelectron; Proteochondroitin Sulfates; Proteoglycans; Rats; Tissue Distribution",
year = "1993",
language = "English",
volume = "43",
pages = "79--84",
journal = "Kidney International",
issn = "0085-2538",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - Basement membrane proteoglycans and development.

AU - Couchman, J R

AU - Abrahamson, D R

AU - McCarthy, K J

N1 - Keywords: Animals; Basement Membrane; Diabetes Mellitus, Experimental; Heparan Sulfate Proteoglycans; Heparitin Sulfate; Kidney; Microscopy, Immunoelectron; Proteochondroitin Sulfates; Proteoglycans; Rats; Tissue Distribution

PY - 1993

Y1 - 1993

N2 - Basement membranes contain distinct collagen, glycoprotein and proteoglycan species, and these exhibit considerable heterogeneity in isoform or type when different tissue types are compared. Additionally, many components are differentially expressed in organogenesis. We have considered the distributions in glomerulogenesis of two distinct basement membrane proteoglycans, a small heparan sulfate proteoglycan and a chondroitin sulfate proteoglycan (BM-CSPG). While the former was present in all kidney basement membranes through development, the latter was apparently regulated in distribution. BM-CSPG was only strongly expressed in the vasculature invading late comma stage glomeruli, and later in presumptive and mature Bowman's capsule. Over the first six to eight weeks, the capillary basement membranes contained BM-CSPG, but in gradually decreasing amounts until it became completely undetectable. The basement membrane of the adult rat glomerulus is unique in its lack of BM-CSPG. However, in diabetic rats, BM-CSPG is apparently re-expressed in the glomerular basement membrane, a potential marker for pathological changes in glomerular structure. While its function awaits elucidation, BM-CSPG may be essential for basement membrane integrity or stability and have important roles in kidney development.

AB - Basement membranes contain distinct collagen, glycoprotein and proteoglycan species, and these exhibit considerable heterogeneity in isoform or type when different tissue types are compared. Additionally, many components are differentially expressed in organogenesis. We have considered the distributions in glomerulogenesis of two distinct basement membrane proteoglycans, a small heparan sulfate proteoglycan and a chondroitin sulfate proteoglycan (BM-CSPG). While the former was present in all kidney basement membranes through development, the latter was apparently regulated in distribution. BM-CSPG was only strongly expressed in the vasculature invading late comma stage glomeruli, and later in presumptive and mature Bowman's capsule. Over the first six to eight weeks, the capillary basement membranes contained BM-CSPG, but in gradually decreasing amounts until it became completely undetectable. The basement membrane of the adult rat glomerulus is unique in its lack of BM-CSPG. However, in diabetic rats, BM-CSPG is apparently re-expressed in the glomerular basement membrane, a potential marker for pathological changes in glomerular structure. While its function awaits elucidation, BM-CSPG may be essential for basement membrane integrity or stability and have important roles in kidney development.

M3 - Journal article

C2 - 8433574

VL - 43

SP - 79

EP - 84

JO - Kidney International

JF - Kidney International

SN - 0085-2538

IS - 1

ER -

ID: 5165914