TULP3 Regulates Proliferation and Differentiation of 3T3-L1 Preadipocytes Through the Hedgehog Signaling Pathway

Xinlin Jin1, Yu Zhang1, Yunzhou Wang2

  • 1Shandong Provincial Key Laboratory for Livestock Germplasm Innovation & Utilization, College of Animal Science and Technology, Shandong Agricultural University, Tai'an 271018, China.

Biology
|April 26, 2025
PubMed

Insights

Tubulin polymerization-depolymerizing protein 3 (TULP3) promotes adipocyte differentiation by inhibiting the Hedgehog signaling pathway. This finding offers insights into treating adipose tissue dysfunction and related diseases.

Area of Science:

  • Cell Biology
  • Molecular Biology
  • Biochemistry

Background:

  • The TULP family, including TULP3, is known from obese mice studies and tumor cell research.
  • The specific role of TULP3 in adipocytes and its mechanism of action in adipose tissue remain largely unexplored.

Purpose of the Study:

  • To investigate the role and mechanism of TULP3 in the differentiation of adipocytes.
  • To determine if TULP3 influences adipogenesis via the Hedgehog signaling pathway.

Main Methods:

  • Utilized 3T3-L1 cells to study TULP3 expression during adipocyte differentiation.
  • Manipulated TULP3 expression (overexpression and inhibition) to assess its impact on cell proliferation and differentiation.
  • Investigated the interaction between TULP3 and the Hedgehog signaling pathway in adipogenesis.

Main Results:

  • TULP3 expression increased during 3T3-L1 cell differentiation.
  • Overexpression of TULP3 enhanced adipocyte proliferation and differentiation, while inhibition had the opposite effect.
  • TULP3 was identified as a negative regulator of the Hedgehog signaling pathway, promoting adipogenic differentiation by inhibiting pathway activity.

Conclusions:

  • TULP3 plays a crucial role in promoting adipogenic differentiation of precursor adipocytes.
  • Inhibition of the Hedgehog signaling pathway by TULP3 is a key mechanism in adipogenesis.
  • These findings provide valuable information for understanding adipocytogenesis and developing treatments for adipose tissue dysfunction and related diseases.

Related Concept Videos

Hedgehog Signaling Pathway02:33

Hedgehog Signaling Pathway

The Hedgehog gene (Hh) was first discovered due to its control of the growth of disorganized, hair-like bristles phenotype in Drosophila, much like hedgehog spines. Hh plays a crucial role in the development of organs and the maintenance of homeostasis in both invertebrates and vertebrates. However, while Drosophila has only one Hh protein, mammals have multiple functional Hedgehog proteins - Sonic (Shh), Desert (Dhh), and Indian Hedgehog (Ihh). All of these homologous proteins have adapted to...
Regulation of Angiogenesis and Blood Supply01:24

Regulation of Angiogenesis and Blood Supply

Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl hydroxylase and factor...
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a rapamycin-insensitive companion...
TGF - β Signaling Pathway01:16

TGF - β Signaling Pathway

The TGF-β signaling pathway regulates cell growth, differentiation, adhesion, motility, and development. TGF-β ligands that induce TGF-β signaling are synthesized in their latent form. Several proteases or cell surface receptors such as integrins act upon the latent form, releasing the active ligand. There are three types of mammalian TGF-βs: (TGF-β1, TGF-β2, and TGF-β3) that bind as homodimers or heterodimers to TGF-β receptors. The TGF-β receptors are of three kinds RI, RII, and RIII. The RI...
Hedgehog Signaling Pathway02:33

Hedgehog Signaling Pathway

The Hedgehog gene (Hh) was first discovered due to its control of the growth of disorganized, hair-like bristles phenotype in Drosophila, much like hedgehog spines. Hh plays a crucial role in the development of organs and the maintenance of homeostasis in both invertebrates and vertebrates. However, while Drosophila has only one Hh protein, mammals have multiple functional Hedgehog proteins - Sonic (Shh), Desert (Dhh), and Indian Hedgehog (Ihh). All of these homologous proteins have adapted to...
Role Of Notch Signalling In Intestinal Stem Cell Renewal01:12

Role Of Notch Signalling In Intestinal Stem Cell Renewal

Notch signaling was first discovered in Drosophila melanogaster, where it is involved in cell lineage differentiation. Notch signaling regulates the maintenance and differentiation of intestinal stem cells or ISCs by controlling the expression of atonal homolog 1 or Atoh1. Atoh1 directs cells to differentiate into secretory cells.
Direct cell-to-cell contact is needed for the activation of Notch signaling. The signal is initiated when a notch ligand binds to a receptor on an adjacent cell, also...