TY - JOUR
T1 - Protein composition and movements of membrane swellings associated with primary cilia
AU - Mohieldin, Ashraf M.
AU - Haymour, Hanan S.
AU - Lo, Shao T.
AU - Aboualaiwi, Wissam A.
AU - Atkinson, Kimberly F.
AU - Ward, Christopher J.
AU - Gao, Min
AU - Wessely, Oliver
AU - Nauli, Surya M.
N1 - Funding Information:
This work partially fulfills the requirements of a PhD degree in Medicinal and Biological Chemistry for Ashraf M. Mohieldin. This work was supported by the Department of Defense PR130153 (SMN) and in part by the National Institute of Health R01DK080640 (SMN), R01DK080745 (OW) and F31DK096870 (AMM).
Publisher Copyright:
© 2015 Springer Basel.
PY - 2015/6/26
Y1 - 2015/6/26
N2 - Abstract Dysfunction of many ciliary proteins has been linked to a list of diseases, from cystic kidney to obesity and from hypertension to mental retardation. We previously proposed that primary cilia are unique communication organelles that function as microsensory compartments that house mechanosensory molecules. Here we report that primary cilia exhibit membrane swellings or ciliary bulbs, which based on their unique ultrastructure and motility, could be mechanically regulated by fluid-shear stress. Together with the ultrastructure analysis of the swelling, which contains monosialodihexosylganglioside (GM3), our results show that ciliary bulb has a distinctive set of functional proteins, including GM3 synthase (GM3S), bicaudal-c1 (Bicc1), and polycystin-2 (PC2). In fact, results from our cilia isolation demonstrated for the first time that GM3S and Bicc1 are members of the primary cilia proteins. Although these proteins are not required for ciliary membrane swelling formation under static condition, fluid-shear stress induced swelling formation is partially modulated by GM3S. We therefore propose that the ciliary bulb exhibits a sensory function within the mechano-ciliary structure. Overall, our studies provided an important step towards understanding the ciliary bulb function and structure.
AB - Abstract Dysfunction of many ciliary proteins has been linked to a list of diseases, from cystic kidney to obesity and from hypertension to mental retardation. We previously proposed that primary cilia are unique communication organelles that function as microsensory compartments that house mechanosensory molecules. Here we report that primary cilia exhibit membrane swellings or ciliary bulbs, which based on their unique ultrastructure and motility, could be mechanically regulated by fluid-shear stress. Together with the ultrastructure analysis of the swelling, which contains monosialodihexosylganglioside (GM3), our results show that ciliary bulb has a distinctive set of functional proteins, including GM3 synthase (GM3S), bicaudal-c1 (Bicc1), and polycystin-2 (PC2). In fact, results from our cilia isolation demonstrated for the first time that GM3S and Bicc1 are members of the primary cilia proteins. Although these proteins are not required for ciliary membrane swelling formation under static condition, fluid-shear stress induced swelling formation is partially modulated by GM3S. We therefore propose that the ciliary bulb exhibits a sensory function within the mechano-ciliary structure. Overall, our studies provided an important step towards understanding the ciliary bulb function and structure.
KW - Bicc-1
KW - Ciliary bulb
KW - Ciliary membrane swelling
KW - Fluid-shear stress
KW - GM3S
KW - PC2
KW - Primary cilia
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U2 - 10.1007/s00018-015-1838-x
DO - 10.1007/s00018-015-1838-x
M3 - Article
C2 - 25650235
AN - SCOPUS:84926467684
SN - 1420-682X
VL - 72
SP - 2415
EP - 2429
JO - Cellular and Molecular Life Sciences
JF - Cellular and Molecular Life Sciences
IS - 12
M1 - 1838
ER -