Membrane Lipids in Epithelial Polarity: Sorting out the PIPs

被引:4
作者
Gwilt, Katlynn Bugda [1 ]
Thiagarajah, Jay R. [1 ]
机构
[1] Boston Childrens Hosp, Harvard Med Sch, Div Gastroenterol Hepatol & Nutr, Boston, MA 02115 USA
关键词
polarity; phosphoinositide; epithelial; apical; PI-kinase; phosphatase; TTC7; glycosphingolipid; LUMEN FORMATION; PLASMA-MEMBRANE; CELL POLARITY; PHOSPHATIDYLINOSITOL; 4-KINASE; STRUCTURAL BASIS; MULTIPLE ROLES; APICAL SURFACE; PROTEINS; PHOSPHOINOSITIDES; PHOSPHATIDYLSERINE;
D O I
10.3389/fcell.2022.893960
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The development of cell polarity in epithelia, is critical for tissue morphogenesis and vectorial transport between the environment and the underlying tissue. Epithelial polarity is defined by the development of distinct plasma membrane domains: the apical membrane interfacing with the exterior lumen compartment, and the basolateral membrane directly contacting the underlying tissue. The de novo generation of polarity is a tightly regulated process, both spatially and temporally, involving changes in the distribution of plasma membrane lipids, localization of apical and basolateral membrane proteins, and vesicular trafficking. Historically, the process of epithelial polarity has been primarily described in relation to the localization and function of protein 'polarity complexes.' However, a critical and foundational role is emerging for plasma membrane lipids, and in particular phosphoinositide species. Here, we broadly review the evidence for a primary role for membrane lipids in the generation of epithelial polarity and highlight key areas requiring further research. We discuss the complex interchange that exists between lipid species and briefly examine how major membrane lipid constituents are generated and intersect with vesicular trafficking to be preferentially localized to different membrane domains with a focus on some of the key protein-enzyme complexes involved in these processes.
引用
收藏
页数:12
相关论文
共 106 条
[81]   Phosphoinositides in Cell Architecture [J].
Shewan, Annette ;
Eastburn, Dennis J. ;
Mostov, Keith .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2011, 3 (08) :1-17
[82]   Apical phosphatidylserine externalization in auditory hair cells [J].
Shi, Xiaorui ;
Gillespie, Peter G. ;
Nuttall, Alfred L. .
MOLECULAR MEMBRANE BIOLOGY, 2007, 24 (01) :16-27
[83]   Flipping the dogma - phosphatidylserine in non-apoptotic cell death [J].
Shlomovitz, Inbar ;
Speir, Mary ;
Gerlic, Motti .
CELL COMMUNICATION AND SIGNALING, 2019, 17 (01)
[84]   Molecular mechanisms of de novo lumen formation [J].
Sigurbjoernsdottir, Sara ;
Mathew, Renjith ;
Leptin, Maria .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2014, 15 (10) :665-676
[85]   Great Expectations for PIP: Phosphoinositides as Regulators of Signaling During Development and Disease [J].
Skwarek, Lara C. ;
Boulianne, Gabrielle L. .
DEVELOPMENTAL CELL, 2009, 16 (01) :12-20
[86]  
Sohn Mira, 2016, J Rare Dis Res Treat, V2, P47, DOI 10.29245/2572-9411/2017/1.1080
[87]   aPKC restricts the basolateral determinant PtdIns(3,4,5)P3 to the basal region [J].
Takahama, Shoukichi ;
Hirose, Tomonori ;
Ohno, Shigeo .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 368 (02) :249-255
[88]   PI4KIIIα is required for cortical integrity and cell polarity during Drosophila oogenesis [J].
Tan, Julie ;
Oh, Karen ;
Burgess, Jason ;
Hipfner, David R. ;
Brill, Julie A. .
JOURNAL OF CELL SCIENCE, 2014, 127 (05) :954-966
[89]   Structural basis for NHERF recognition by ERM proteins [J].
Terawaki, S ;
Maesaki, R ;
Hakoshima, T .
STRUCTURE, 2006, 14 (04) :777-789
[90]   A genetic screen for aminophospholipid transport mutants identifies the phosphatidylinositol 4-kinase, Stt4p, as an essential component in phosphatidylserine metabolism [J].
Trotter, PJ ;
Wu, WI ;
Pedretti, J ;
Yates, R ;
Voelker, DR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (21) :13189-13196