Cited by 235melanin and skin pigmentationZebrafish Biomedical Research ApplicationsDevelopmental Biology and Gene Regulation

Thyroid hormone-dependent adult pigment cell lineage and pattern in zebrafish

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McMenamin, Sarah K., Bain, Emily J., McCann, Anna E., Patterson, Larissa B., Eom, Dae Seok, Waller, Zachary P., Hamill, James C., Kuhlman, Julie A. +2 more·2014·Science

Abstract

Origin of fish pigment cell for pattern: Zebrafish stripes arise from the interactions of pigment cells: black melanophores, iridescent iridophores, and yellow-orange xanthophores. Melanophores and iridophores develop from nerve-associated stem cells, but the origin of xanthophores is unclear. Two studies now reveal that adult xanthophores originate from xanthophores in embryonic and larval fish, when they proliferate to cover the skin before the arrival of black and silver cells in a striped arrangement. Mahalwar et al. show that xanthophores change their final shape and color depending on their location. In black cells, xanthophores appear faint and stellate, but in silver cells, they are bright and compact. Precise superposition creates the blue and golden colors. McMenamin et al. observe the loss of pigment in embryonic xanthophores and the later reappearance in the adult. They show that redifferentiation depends on the thyroid hormone that also limits melanophore population expansion. Science , this issue p. 1362 and p. 1358

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  • Adult melanophores arise from a transit-amplifying progenitor.

    “In contrast to adult melanophores that arise from a transit-amplifying progenitor”

    From Thyroid hormone regulates distinct paths to maturation in pigment cell lineages (2019) · cites this paper as McMenamin et al., 2014

    The passage labeled Abstract (page unavailable) says adult body melanophores arise from extra-hypodermal, peripheral nerve-associated precursors and describes presumptive melanophore precursors differentiating. It does not identify those precursors as transit-amplifying, so the specific progenitor type is unsupported. (LLM, conf=0.83)

    Experimental — accuracy not yet measured
  • Melanophores of euthyroid fish fail to divide whereas those of hypothyroid fish continue to divide.

    “Prior analyses indicated that melanophores of euthyroid fish fail to divide whereas those of hypothyroid fish continue to do so (McMenamin et al., 2014).”

    From Thyroid hormone regulates distinct paths to maturation in pigment cell lineages (2019) · cites this paper as McMenamin et al., 2014

    The indexed passage labeled Abstract reports that melanophores in euthyroid larvae rarely divided, while those in hypothyroid larvae divided frequently. It supports the comparison, but “fail to divide” overstates the finding that division was rare, not absent. (LLM, conf=0.88)

    Experimental — accuracy not yet measured
  • Fish lacking thyroid hormone have about twice the normal number of melanophores and lack visible xanthophores.

    “fish lacking TH have about twice the normal number of melanophores and lack visible xanthophores (Figure 1A) (McMenamin et al., 2014).”

    From Thyroid hormone regulates distinct paths to maturation in pigment cell lineages (2019) · cites this paper as McMenamin et al., 2014

    The passage labeled Abstract (no page supplied), describing Fig. 1, reports that fish thyroid-ablated early in development lacked adult body xanthophores and had excess melanophores. It does not quantify the excess as about twice the normal number. It also notes that some xanthophores developed later, so their absence is not permanent. (LLM, conf=0.86)

    Experimental — accuracy not yet measured
  • Melanoblasts derived from peripheral-nerve associated progenitors are proliferative during adult pigment pattern formation, but this activity largely ceases as the cells differentiate.

    “Melanoblasts derived from peripheral-nerve associated progenitors are proliferative during adult pigment pattern formation yet this activity largely ceases as the cells differentiate (Budi et al., 2011; McMenamin et al., 2014).”

    From Thyroid hormone regulates distinct paths to maturation in pigment cell lineages (2019) · cites this paper as McMenamin et al., 2014

    The passage labeled Abstract says adult melanophores arise from peripheral nerve-associated precursors. It also reports that melanophores rarely divided in euthyroid larvae, but it does not establish that their precursors proliferate or that proliferation ceases as they differentiate; melanophores divided frequently in hypothyroid larvae. (LLM, conf=0.85)

    Experimental — accuracy not yet measured
  • Addition of exogenous thyroid hormone to hypothyroid cells ex vivo can promote differentiation of unpigmented melanoblasts to melanophores.

    “Indeed, prior analyses showed that addition of exogenous TH to hypothyroid cells ex vivo can promote differentiation of unpigmented melanoblasts to melanophores (McMenamin et al., 2014), contrary to the idea that TH specifically blocks melanophore development.”

    From Thyroid hormone regulates distinct paths to maturation in pigment cell lineages (2019) · cites this paper as McMenamin et al., 2014

    In the passage labeled Abstract (page unavailable), the paper reports that melanophore precursors in hypothyroid larvae were less likely to differentiate and concludes that TH promotes their differentiation. It does not report adding TH to hypothyroid cells ex vivo or observing unpigmented melanoblasts become melanophores in that setting. (LLM, conf=0.86)

    Experimental — accuracy not yet measured

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Cites

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Authors
McMenamin, S. K., Bain, E. J., McCann, A. E., Patterson, L. B., Eom, D. S., Waller, Z. P., Hamill, J. C., Kuhlman, J. A., Eisen, J. S., & Parichy, D. M.
Affiliations
  • University of Washington (US)
  • Iowa State University (US)
  • University of Oregon (US)
Corresponding author
Parichy, David M.
Venue
Science
Published
2014-09-12
Volume
345
Issue
6202
Pages
1358-1361
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W1999753634
Cited by
235
References
0
Citations by year
2026: 14 · 2025: 15 · 2024: 27 · 2023: 25 · 2022: 21 · 2021: 30 · 2020: 16 · 2019: 24 · 2018: 16 · 2017: 15 · 2016: 12 · 2015: 15 · 2014: 5
FWCI
7.23
Type
journal article
Language
en
Open access
Locations
  • Science (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
  • eScholarship (California Digital Library) (submittedVersion)
Funders
  • National Institute of General Medical Sciences (R01GM096906, K99GM105874, R01GM062182, F32GM090362, R01GM111233)
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (T32HD007183, P01HD022486, R03HD074787)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › melanin and skin pigmentation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Zebrafish Biomedical Research Applications
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
Keywords
zebrafish, xanthophores, melanophores, iridophores, stripe pattern formation, thyroid hormones, redifferentiation
MeSH terms
Animals, Cell Differentiation, Embryo, Nonmammalian, Melanophores, Skin Pigmentation, Thyroid Hormones, Zebrafish, Cell Lineage, Body Patterning

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