THE ROLE OF DETERMINING THE LEVELS OF SERUM COLLAGEN TYPE IV IN DIAGNOSING EARLY DIABETIC NEPHROPATHY

Renal Failure ◽  
2002 ◽  
Vol 24 (6) ◽  
pp. 747-753 ◽  
Author(s):  
Xunhui Xu ◽  
Zhaolong Wu ◽  
Qin Zhou ◽  
Yiwen Zhang ◽  
Dan Wu
Endocrine ◽  
2010 ◽  
Vol 39 (3) ◽  
pp. 251-258 ◽  
Author(s):  
Qiangxiang Li ◽  
Xiang Ao ◽  
Youhong Du ◽  
Yang Li ◽  
Yangshi Ou ◽  
...  

2019 ◽  
Vol 317 (6) ◽  
pp. F1680-F1694 ◽  
Author(s):  
Gek Cher Chan ◽  
Diana G. Eng ◽  
Jeffrey H. Miner ◽  
Charles E. Alpers ◽  
Kelly Hudkins ◽  
...  

In healthy glomeruli, parietal epithelial cell (PEC)-derived extracellular matrix (ECM) proteins include laminin-β1, perlecan, and collagen type IV-α2 and podocyte-specific ECM proteins include laminin-β2, agrin, and collagen type IV-α4. This study aimed to define individual ECM protein isoform expression by PECs in both experimental and human focal segmental glomerulosclerosis (FSGS) and diabetic nephropathy (DN) and to determine if changes were CD44 dependent. In experimental FSGS induced with a cytotoxic podocyte antibody and in the BTBR ob/ob mouse model of DN, PEC-derived protein staining was significantly increased in PECs. Dual staining also showed de novo expression of the podocyte-specific ECM proteins laminin-β2 and agrin in PECs. Similar findings were observed in biopsies from patients with FSGS and DN. Increases in individual ECM proteins colocalized with CD44 in PECs in disease. To determine the role of CD44, FSGS was induced in CD44−/− and CD44+/+ mice. PEC staining for perlecan, collagen type IV-α2, laminin-β2, and agrin were significantly lower in diseased CD44−/− mice compared with diseased CD44+/+ mice. These results show that in experimental and human FSGS and DN, PECs typically in an activated state, produce both PEC-derived and podocyte-specific ECM protein isoforms, and that the majority of these changes were dependent on CD44.


2016 ◽  
Vol 1 ◽  
pp. 86-92 ◽  
Author(s):  
Asparuh Nikolov ◽  
Ivan Tsinlikov ◽  
Ivanka Tsinlikova ◽  
George Nicoloff ◽  
Alexander Blazhev ◽  
...  

2010 ◽  
Vol 20 (1) ◽  
pp. 34 ◽  
Author(s):  
RW Minz ◽  
A Bakshi ◽  
S Chhabra ◽  
K Joshi ◽  
V Sakhuja

1995 ◽  
Vol 128 (1) ◽  
pp. 127-137 ◽  
Author(s):  
E Tanaka ◽  
M W Kirschner

To understand the role of microtubules in growth cone turning, we observed fluorescently labeled microtubules in neurons as they encountered a substrate boundary. Neurons growing on a laminin-rich substrate avoided growing onto collagen type IV. Turning growth cones assumed heterogeneous morphologies and behaviors that depended primarily in their extent of adhesion to the substrate. We grouped these behaviors into three categories-sidestepping, motility, and growth-mediated reorientation. In sidestepping and motility-mediated reorientation, the growth cone and parts of the axon were not well attached to the substrate so the acquisition of an adherent lamella caused the entire growth cone to move away from the border and consequently reoriented the axon. In these cases, since the motility of the growth cone dominates its reorientation, the microtubules were passive, and reorientation occurred without significant axon growth. In growth-mediated reorientation, the growth cone and axon were attached to the substrate. In this case, microtubules reoriented within the growth cone to stabilize a lamella. Bundling of the reoriented microtubules was followed by growth cone collapse to form new axon, and further, polarized lamellipodial extension. These observations indicate that when the growth cone remains adherent to the substrate during turning, the reorientation and bundling of microtubules is an important, early step in growth cone turning.


2015 ◽  
Vol 229 ◽  
pp. 100-108 ◽  
Author(s):  
Aida A. Korish ◽  
Abdel Galil Abdel Gader ◽  
Hesham M. Korashy ◽  
Abdul Majeed Al-Drees ◽  
Abdulqader A. Alhaider ◽  
...  

2017 ◽  
Vol 45 (2) ◽  
Author(s):  
Ron Maymon ◽  
Sonia Mendlovic ◽  
Yaakov Melcer ◽  
Tal Sarig-Meth ◽  
Lilian Habler ◽  
...  

AbstractObjective:The present study aims to compare the presence and localization of collagen type IV in the prenasal tissue of fetuses with and without Down syndrome (DS).Methods:Products of conception were obtained from mid-gestation uterine evacuations of 14 DS fetuses and 15 unaffected controls. Microdissection of the prenasal area and an analysis of the prenasal tissue specimens were performed by a single pathologist, blinded to the karyotype results. Immunohistological presence and localization of type IV collagen were analyzed in the basement membrane (BM), blood vessels, and stroma of the tissues.Results:There were no statistically significant differences in the presence and localization of antibodies for collagen IV in the blood vessels and stroma between the two groups. However, the presence and localization of type IV collagen in the BM of the prenasal skin were significantly higher in DS specimens compared to the control group (P=0.023). When combining both groups altogether, a significant correlation was found between the increased prenasal thickness (PT) and the high presence and location of collagen type IV, irrespective of the karyotype results (Spearman’s correlation; R=0.459; P=0.012).Conclusion:Using the immunohistochemistry technique, we were able to confirm the overexpression of collagen type IV in the BM of the prenasal area. This may explain the sonographic finding of increased PT seen mainly in DS fetuses.


2016 ◽  
Vol 44 (2) ◽  
pp. 167-172 ◽  
Author(s):  
Sei-ichiro Motegi ◽  
Akiko Sekiguchi ◽  
Chisako Fujiwara ◽  
Sayaka Toki ◽  
Osamu Ishikawa

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