Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Renewal of Intestinal Stem Cells01:23

Renewal of Intestinal Stem Cells

The intestinal epithelial lining rapidly renews every 4 to 5 days. The renewal is facilitated by intestinal stem cells (ISCs) located at the base of the crypt– a gland located at the bottom of each villus. ISCs divide asymmetrically to form new stem cells and progenitor daughter cells. The daughter cells are called transit-amplifying (TA) cells which move upwards along the crypt and either differentiate into absorptive cells– the enterocytes or secretory cells– including the goblet,...
iPS Cell Differentiation01:22

iPS Cell Differentiation

The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

CNOT3 supports ILC2 differentiation and function by destabilizing Tbx21 and Rorc transcripts.

The Journal of experimental medicine·2026
Same author

IL-22 from enteroendocrine cells promotes early-life gut motility in zebrafish through the microbiota.

Science (New York, N.Y.)·2026
Same author

Long-term inhibition of protease hypersensitivity by initial immunological cross-regulation and epigenetic memory in lung stromal cells.

Nature immunology·2026
Same author

Selection for Function in Complex Distributed Pathological Systems.

Evolutionary applications·2026
Same author

Hematopoietic MyD88 orchestrates the control of gut colonization by segmented filamentous bacteria.

Mucosal immunology·2025
Same author

Correction: Perinatal foodborne titanium dioxide exposure-mediated dysbiosis predisposes mice to develop colitis through life.

Particle and fibre toxicology·2024

Related Experiment Video

Updated: May 24, 2026

Directed Differentiation of Induced Pluripotent Stem Cells towards T Lymphocytes
12:47

Directed Differentiation of Induced Pluripotent Stem Cells towards T Lymphocytes

Published on: May 14, 2012

The development of LTi cells.

Marie Cherrier1, Gérard Eberl

  • 1Institut Pasteur, Lymphoid Tissue Development Unit, Paris 75724, France.

Current Opinion in Immunology
|March 6, 2012
PubMed
Summary

Lymphoid tissue inducer (LTi) cells develop fetal lymphoid organs in mammals. Their programming via RORγt enabled pre-birth organogenesis, unlike in other vertebrates.

Area of Science:

  • Immunology
  • Developmental Biology
  • Cell Biology

Background:

  • Lymphoid tissue inducer (LTi) cells are crucial for fetal development of lymph nodes and Peyer's patches.
  • LTi cells share characteristics with Th17 cells, including a pro-inflammatory profile and dependence on the transcription factor RORγt.

Purpose of the Study:

  • To review recent findings on LTi cell development, both in fetal and postnatal stages.
  • To explore the connection between LTi cells and the broader group of innate lymphoid cells (ILCs).
  • To propose a mechanism for the evolution of pre-natal lymphoid organogenesis in mammals.

Main Methods:

  • Review of current scientific literature on LTi cell biology.
  • Comparative analysis of lymphoid organ development across different vertebrate species.

More Related Videos

A Three-dimensional Thymic Culture System to Generate Murine Induced Pluripotent Stem Cell-derived Tumor Antigen-specific Thymic Emigrants
10:44

A Three-dimensional Thymic Culture System to Generate Murine Induced Pluripotent Stem Cell-derived Tumor Antigen-specific Thymic Emigrants

Published on: August 9, 2019

Related Experiment Videos

Last Updated: May 24, 2026

Directed Differentiation of Induced Pluripotent Stem Cells towards T Lymphocytes
12:47

Directed Differentiation of Induced Pluripotent Stem Cells towards T Lymphocytes

Published on: May 14, 2012

A Three-dimensional Thymic Culture System to Generate Murine Induced Pluripotent Stem Cell-derived Tumor Antigen-specific Thymic Emigrants
10:44

A Three-dimensional Thymic Culture System to Generate Murine Induced Pluripotent Stem Cell-derived Tumor Antigen-specific Thymic Emigrants

Published on: August 9, 2019

  • Discussion of the role of transcription factor RORγt in immune cell differentiation.
  • Main Results:

    • LTi cells are essential for initiating the formation of secondary lymphoid organs during mammalian fetal development.
    • The expression of RORγt in specific common lymphoid progenitors is implicated in enabling early lymphoid organ development in mammals.
    • Mammalian pre-natal lymphoid organogenesis contrasts with the infection/injury-induced development in other vertebrates.

    Conclusions:

    • The reprogramming of RORγt in early lymphoid progenitors was a key evolutionary step for mammals, allowing for the development of intrinsic lymphoid structures before birth.
    • Understanding LTi cell development and their relationship with ILCs provides insights into immune system evolution and function.
    • This developmental pathway highlights a significant divergence in immune system organization between mammals and other vertebrates.