Subepithelial telocytes are an important source of Wnts that supports intestinal crypts

被引:405
作者
Shoshkes-Carmel, Michal [1 ,2 ]
Wang, Yue J. [1 ,2 ]
Wangensteen, Kirk J. [1 ,2 ]
Toth, Beata [3 ]
Kondo, Ayano [1 ,2 ]
Massassa, Efi E. [3 ]
Itzkovitz, Shalev [3 ]
Kaestner, Klaus H. [1 ,2 ]
机构
[1] Univ Penn, Perelman Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Ctr Mol Studies Digest & Liver Dis, Philadelphia, PA 19104 USA
[3] Weizmann Inst Sci, Dept Mol Cell Biol, Rehovot, Israel
关键词
STEM-CELLS; TRANSGENIC MICE; EXPRESSION; MOUSE; TRANSCRIPTION; ABLATION; TISSUES; ABSENCE;
D O I
10.1038/s41586-018-0084-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Tissues that undergo rapid cellular turnover, such as the mammalian haematopoietic system or the intestinal epithelium, are dependent on stem and progenitor cells that proliferate to provide differentiated cells to maintain organismal health. Stem and progenitor cells, in turn, are thought to rely on signals and growth factors provided by local niche cells to support their function and self-renewal. Several cell types have been hypothesized to provide the signals required for the proliferation and differentiation of the intestinal stem cells in intestinal crypts(1-6). Here we identify subepithelial telocytes as an important source of Wnt proteins, without which intestinal stem cells cannot proliferate and support epithelial renewal. Telocytes are large but rare mesenchymal cells that are marked by expression of FOXL1 and form a subepithelial plexus that extends from the stomach to the colon. While supporting the entire epithelium, FOXL1(+) telocytes compartmentalize the production of Wnt ligands and inhibitors to enable localized pathway activation. Conditional genetic ablation of porcupine (Porcn), which is required for functional maturation of all Wnt proteins, in mouse FOXL1(+) telocytes causes rapid cessation of Wnt signalling to intestinal crypts, followed by loss of proliferation of stem and transit amplifying cells and impaired epithelial renewal. Thus, FOXL1(+) telocytes are an important source of niche signals to intestinal stem cells.
引用
收藏
页码:242 / +
页数:11
相关论文
共 32 条
[1]
Foxl1-Expressing Mesenchymal Cells Constitute the Intestinal Stem Cell Niche [J].
Aoki, Reina ;
Shoshkes-Carmel, Michal ;
Gao, Nan ;
Shin, Soona ;
May, Catherine L. ;
Goson, Maria L. ;
Zahm, Adam M. ;
Ray, Michael ;
Wiser, Caroline L. ;
Wright, Christopher V. E. ;
Kaestner, Klaus H. .
CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY, 2016, 2 (02) :175-188
[2]
Identification of telocytes in the lamina propria of rat duodenum: transmission electron microscopy [J].
Cantarero Carmona, I. ;
Luesma Bartolome, M. J. ;
Junquera Escribano, C. .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2011, 15 (01) :26-30
[3]
Structural and molecular interrogation of intact biological systems [J].
Chung, Kwanghun ;
Wallace, Jenelle ;
Kim, Sung-Yon ;
Kalyanasundaram, Sandhiya ;
Andalman, Aaron S. ;
Davidson, Thomas J. ;
Mirzabekov, Julie J. ;
Zalocusky, Kelly A. ;
Mattis, Joanna ;
Denisin, Aleksandra K. ;
Pak, Sally ;
Bernstein, Hannah ;
Ramakrishnan, Charu ;
Grosenick, Logan ;
Gradinaru, Viviana ;
Deisseroth, Karl .
NATURE, 2013, 497 (7449) :332-+
[4]
Cretoiu D, 2012, HISTOL HISTOPATHOL, V27, P1067, DOI 10.14670/HH-27.1067
[5]
Functional intestinal stem cells after Paneth cell ablation induced by the loss of transcription factor Math1 (Atoh1) [J].
Durand, Aurelie ;
Donahue, Bridgitte ;
Peignon, Gregory ;
Letourneur, Franck ;
Cagnard, Nicolas ;
Slomianny, Christian ;
Perret, Christine ;
Shroyer, Noah F. ;
Romagnolo, Beatrice .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (23) :8965-8970
[6]
Mesenchymal expression of Fox11, a winged helix transcriptional factor, regulates generation and maintenance of gut-associated lymphoid organs [J].
Fukuda, K ;
Yoshida, H ;
Sato, T ;
Furumoto, T ;
Mizutani-Koseki, Y ;
Suzuki, Y ;
Saito, Y ;
Takemori, T ;
Kimura, M ;
Sato, H ;
Taniguchi, M ;
Nishikawa, S ;
Nakayama, T ;
Koseki, H .
DEVELOPMENTAL BIOLOGY, 2003, 255 (02) :278-289
[7]
Brief Report: CD24 and CD44 Mark Human Intestinal Epithelial Cell Populations with Characteristics of Active and Facultative Stem Cells [J].
Gracz, Adam D. ;
Fuller, Megan K. ;
Wang, Fengchao ;
Li, Linheng ;
Stelzner, Matthias ;
Dunn, James C. Y. ;
Martin, Martin G. ;
Magness, Scott T. .
STEM CELLS, 2013, 31 (09) :2024-2030
[8]
Comparative analysis of RNA-Seq alignment algorithms and the RNA-Seq unified mapper (RUM) [J].
Grant, Gregory R. ;
Farkas, Michael H. ;
Pizarro, Angel D. ;
Lahens, Nicholas F. ;
Schug, Jonathan ;
Brunk, Brian P. ;
Stoeckert, Christian J. ;
Hogenesch, John B. ;
Pierce, Eric A. .
BIOINFORMATICS, 2011, 27 (18) :2518-2528
[9]
Single molecule approaches for quantifying transcription and degradation rates in intact mammalian tissues [J].
Halpern, Keren Bahar ;
Itzkovitz, Shalev .
METHODS, 2016, 98 :134-142
[10]
Bursty Gene Expression in the Intact Mammalian Liver [J].
Halpern, Keren Bahar ;
Tanami, Sivan ;
Landen, Shanie ;
Chapal, Michal ;
Szlak, Liran ;
Hutzler, Anat ;
Nizhberg, Anna ;
Itzkovitz, Shalev .
MOLECULAR CELL, 2015, 58 (01) :147-156