spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

doi: 10.1242/10.1242/jcs.00313


This Article
Right arrow Summary Freely available
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Related articles in JCS
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by McCarthy, R. A.
Right arrow Articles by Argraves, W. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by McCarthy, R. A.
Right arrow Articles by Argraves, W. S.

Megalin and the neurodevelopmental biology of sonic hedgehog and retinol

Robert A. McCarthy and W. Scott Argraves*

Medical University of South Carolina, Department of Cell Biology, 171 Ashley Avenue, Charleston, SC 29425-2204, USA



View larger version (17K):

[in a new window]
 
Fig. 1. Schematic diagram depicting the modular structure of megalin. Megalin (LRP-2) is a large, ~600 kDa integral membrane protein belonging to the LDL receptor gene family [for a review of the LDL receptor gene family see (Nykjaer and Willnow, 2002Go; Strickland et al., 2002Go)]. Its cytoplasmic domain contains PxxP, NPxY, YxxM and LL elements that are thought to be involved in the endocytosis and signaling activities of the receptor. Numerous adaptor molecules have been shown to interact with the megalin cytoplasmic domain including proteins with PTB, PDZ domains as well as ones with ankyrin and tetratrico repeat elements (Gotthardt et al., 2000Go; Petersen et al., 2003Go; Rader et al., 2000Go). The ectodomain of megalin comprises several distinct domains or sequence motifs including ligand-binding-type cysteine-rich repeats (complement-like), epidermal growth factor type cysteine-rich repeats and YWTD domains [each group of six YWTD repeats folds into a beta-propeller structure (Springer, 1998Go)].

 


View larger version (32K):

[in a new window]
 
Fig. 2. Possible ways in which megalin might influence N-Shh trafficking and signaling. The mechanisms include direct signaling via megalin [the asterisk indicates megalin-binding adaptor proteins of the fetal brain (Petersen et al., 2003Go)], megalin-mediated endocytosis and trafficking of N-Shh leading to N-Shh transcytosis and megalin-mediated trafficking of the N-Shh receptors Ptc and Smo. Not depicted in the model are heparan sulfate proteoglycans, which have been shown to cooperate with megalin in N-Shh endocytosis (McCarthy et al., 2002Go).

 





© The Company of Biologists Ltd 2003