The Left-Right Pitx2 Pathway Drives Organ-Specific Arterial and Lymphatic Development in the Intestine

被引:77
|
作者
Mahadevan, Aparna [1 ]
Welsh, Ian C. [1 ]
Sivakumar, Aravind [1 ]
Gludish, David W. [2 ]
Shilvock, Abigail R. [1 ]
Noden, Drew M. [3 ]
Huss, David [4 ,5 ]
Lansford, Rusty [4 ,5 ]
Kurpios, Natasza A. [1 ]
机构
[1] Cornell Univ, Coll Vet Med, Dept Mol Med, Ithaca, NY 14853 USA
[2] Cornell Univ, Dept Microbiol & Immunol, Coll Vet Med, Ithaca, NY 14853 USA
[3] Cornell Univ, Dept Biomed Sci, Coll Vet Med, Ithaca, NY 14853 USA
[4] Univ So Calif, Keck Sch Med, Childrens Hosp Los Angeles, Saban Res Inst,Dev Neurosci Program, Los Angeles, CA 90027 USA
[5] Univ So Calif, Keck Sch Med, Childrens Hosp Los Angeles, Dept Radiol,Saban Res Inst, Los Angeles, CA 90027 USA
关键词
CHEMOKINE RECEPTOR CXCR4; ORIGIN; VASCULATURE; SYSTEM; MOUSE; GUT; MORPHOGENESIS; ANGIOGENESIS; ZEBRAFISH; CXCL12;
D O I
10.1016/j.devcel.2014.11.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The dorsal mesentery (DM) is the major conduit for blood and lymphatic vessels in the gut. The mechanisms underlying their morphogenesis are challenging to study and remain unknown. Here we show that arteriogenesis in the DM begins during gut rotation and proceeds strictly on the left side, dependent on the Pitx2 target gene Cxcl12. Although competent Cxcr4-positive angioblasts are present on the right, they fail to form vessels and progressively emigrate. Surprisingly, gut lymphatics also initiate in the left DM and arise only after-and dependent on-arteriogenesis, implicating arteries as drivers of gut lymphangiogenesis. Our data begin to unravel the origin of two distinct vascular systems and demonstrate how early left-right molecular asymmetries are translated into organ-specific vascular patterns. We propose a dual origin of gut lymphangiogenesis in which prior arterial growth is required to initiate local lymphatics that only subsequently connect to the vascular system.
引用
收藏
页码:690 / 706
页数:17
相关论文
共 23 条
  • [1] Pitx2: a left-right asymmetric signalling molecule
    Liu, JL
    Tan, Y
    PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS, 1999, 26 (01) : 3 - 5
  • [2] Pitx2 participates in the late phase of the pathway controlling left-right asymmetry
    Piedra, ME
    Icardo, JM
    Albajar, M
    Rodriguez-Rey, JC
    Ros, MA
    CELL, 1998, 94 (03) : 319 - 324
  • [4] Pitx2 determines left-right asymmetry of internal organs in vertebrates
    Ryan, AK
    Blumberg, B
    Rodriguez-Esteban, C
    Yonei-Tamura, S
    Tamura, K
    Tsukui, T
    de la Peña, J
    Sabbagh, W
    Greenwald, J
    Choe, S
    Norris, DP
    Robertson, EJ
    Evans, RM
    Rosenfeld, MG
    Belmonte, JCI
    NATURE, 1998, 394 (6693) : 545 - 551
  • [5] Vertebrate left-right asymmetry: The role of the homeobox gene PITX2
    Blum, M
    Schweickert, A
    Campione, M
    Nowotschin, S
    Fischer, A
    Viebahn, C
    van Bebber, F
    Hafter, P
    Steinbeisser, H
    DEVELOPMENTAL BIOLOGY, 1999, 210 (01) : 233 - 233
  • [6] Mesendoderm and left-right brain, heart and gut development are differentially regulated by pitx2 isoforms
    Essner, JJ
    Branford, WW
    Zhang, J
    Yost, HJ
    DEVELOPMENT, 2000, 127 (05): : 1081 - 1093
  • [7] The role of Pitx2 during cardiac development -: Linking left-right signaling and congenital heart diseases
    Franco, D
    Campione, M
    TRENDS IN CARDIOVASCULAR MEDICINE, 2003, 13 (04) : 157 - 163
  • [8] Pitx2 isoforms:: involvement of Pitx2c but not Pitx2a or Pitx2b in vertebrate left-right asymmetry
    Schweickert, A
    Campione, M
    Steinbeisser, H
    Blum, M
    MECHANISMS OF DEVELOPMENT, 2000, 90 (01) : 41 - 51
  • [9] Integration of Left-Right Pitx2 Transcription and Wnt Signaling Drives Asymmetric Gut Morphogenesis via Daam2
    Welsh, Ian C.
    Thomsen, Michael
    Gludish, David W.
    Alfonso-Parra, Catalina
    Bai, Yan
    Martin, James F.
    Kurpios, Natasza A.
    DEVELOPMENTAL CELL, 2013, 26 (06) : 629 - 644
  • [10] The transcription factor Pitx2 mediates situs-specific morphogenesis in response to left-right asymmetric signals
    Logan, M
    Pagán-Westphal, SM
    Smith, DM
    Paganessi, L
    Tabin, CJ
    CELL, 1998, 94 (03) : 307 - 317