New concepts in basement membrane biology

被引:123
作者
Halfter, Willi [1 ]
Oertle, Philipp [2 ,3 ]
Monnier, Christophe A. [2 ,3 ]
Camenzind, Leon [2 ,3 ]
Reyes-Lua, Magaly [1 ]
Hu, Huaiyu [4 ]
Candiello, Joseph [5 ]
Labilloy, Anatalia [6 ]
Balasubramani, Manimalha [7 ]
Henrich, Paul Bernhard [1 ]
Plodinec, Marija [2 ,3 ,8 ]
机构
[1] Univ Basel Hosp, Dept Ophthalmol, CH-4031 Basel, Switzerland
[2] Univ Basel, Biozentrum, CH-4003 Basel, Switzerland
[3] Univ Basel, Swiss Nanosci Inst, CH-4003 Basel, Switzerland
[4] SUNY Syracuse, Dept Neurobiol & Physiol, Upstate Univ Hosp, Syracuse, NY USA
[5] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA 15260 USA
[6] Univ Pittsburgh, Dept Renal Physiol, Pittsburgh, PA 15260 USA
[7] Univ Pittsburgh, Proteom Core Facil, Pittsburgh, PA 15260 USA
[8] Univ Basel Hosp, Dept Pathol, Basel, Switzerland
关键词
basal lamina; basement membrane; biomechanical properties; collagen IV; laminin; membrane asymmetry; nidogen; perlecan; HEPARAN-SULFATE PROTEOGLYCAN; ANTERIOR LENS CAPSULE; IV COLLAGEN; BIOMECHANICAL PROPERTIES; MICE LACKING; MOUSE MODEL; LAMININ; PROTEIN; BRAIN; EXPRESSION;
D O I
10.1111/febs.13495
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Basement membranes (BMs) are thin sheets of extracellular matrix that outline epithelia, muscle fibers, blood vessels and peripheral nerves. The current view of BM structure and functions is based mainly on transmission electron microscopy imaging, in vitro protein binding assays, and phenotype analysis of human patients, mutant mice and invertebrata. Recently, MS-based protein analysis, biomechanical testing and cell adhesion assays with in vivo derived BMs have led to new and unexpected insights. Proteomic analysis combined with ultrastructural studies showed that many BMs undergo compositional and structural changes with advancing age. Atomic force microscopy measurements in combination with phenotype analysis have revealed an altered mechanical stiffness that correlates with specific BM pathologies in mutant mice and human patients. Atomic force microscopy-based height measurements strongly suggest that BMs are more than two-fold thicker than previously estimated, providing greater freedom for modelling the large protein polymers within BMs. In addition, data gathered using BMs extracted from mutant mice showed that laminin has a crucial role in BM stability. Finally, recent evidence demonstrate that BMs are bi-functionally organized, leading to the proposition that BM-sidedness contributes to the alternating epithelial and stromal tissue arrangements that are found in all metazoan species. We propose that BMs are ancient structures with tissue-organizing functions and were essential in the evolution of metazoan species.
引用
收藏
页码:4466 / 4479
页数:14
相关论文
共 105 条
  • [21] Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly
    Gould, DB
    Phalan, FC
    Breedveld, GJ
    van Mil, SE
    Smith, RS
    Schimenti, JC
    Aguglia, U
    van der Knaap, MS
    Heutink, P
    John, SWM
    [J]. SCIENCE, 2005, 308 (5725) : 1167 - 1171
  • [22] Col4a1 mutation causes endoplasmic reticulum stress and genetically modifiable ocular dysgenesis
    Gould, Douglas B.
    Marchant, Jeffrey K.
    Savinova, Olga V.
    Smith, Richard S.
    John, Simon W. M.
    [J]. HUMAN MOLECULAR GENETICS, 2007, 16 (07) : 798 - 807
  • [23] β1-class integrins regulate the development of laminae and folia in the cerebral and cerebellar cortex
    Graus-Porta, D
    Blaess, S
    Senften, M
    Littlewood-Evans, A
    Damsky, C
    Huang, Z
    Orban, P
    Klein, R
    Schittny, JC
    Müller, U
    [J]. NEURON, 2001, 31 (03) : 367 - 379
  • [24] Cell invasion through basement membrane: the anchor cell breaches the barrier
    Hagedorn, Elliott J.
    Sherwood, David R.
    [J]. CURRENT OPINION IN CELL BIOLOGY, 2011, 23 (05) : 589 - 596
  • [25] Basement membrane-dependent survival of retinal ganglion cells
    Halfter, W
    Willem, M
    Mayer, U
    [J]. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2005, 46 (03) : 1000 - 1009
  • [26] Collagen XVIII is a basement membrane heparan sulfate proteoglycan
    Halfter, W
    Dong, SC
    Schurer, B
    Cole, GJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (39) : 25404 - 25412
  • [27] Halfter W, 2002, J NEUROSCI, V22, P6029
  • [28] Halfter W, 1987, J NEUROSCI, V37, P12
  • [29] An organizing function of basement membranes in the developing nervous system
    Halfter, Willi
    Yip, Joseph
    [J]. MECHANISMS OF DEVELOPMENT, 2014, 133 : 1 - 10
  • [30] The Bi-Functional Organization of Human Basement Membranes
    Halfter, Willi
    Monnier, Christophe
    Mueller, David
    Oertle, Philipp
    Uechi, Guy
    Balasubramani, Manimalha
    Safi, Farhad
    Lim, Roderick
    Loparic, Marko
    Henrich, Paul Bernhard
    [J]. PLOS ONE, 2013, 8 (07):