Thyroid hormone-dependent adult pigment cell lineage and pattern in zebrafish
Open accessAbstract
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 measuredMelanophores 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 measuredFish 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 measuredMelanoblasts 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 measuredAddition 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
Most adult xanthophores develop directly from embryonic-early larval xanthophores that lose their pigment and then reacquire it late in adult pattern formation.
“Most adult xanthophores develop directly from EL xanthophores that lose their pigment and then reacquire it late in adult pattern formation (Figure 3A) (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 fate-mapping passage (section labeled Abstract; page unavailable) says that some adult xanthophores arise directly from embryonic/early larval xanthophores that lose pigment and later reacquire it. It also identifies an independent source of adult xanthophores and does not establish that the embryonic/early larval lineage accounts for most of them. (LLM, conf=0.88)
Experimental — accuracy not yet measuredThyroid hormone promotes the melanization of melanoblasts ex vivo.
“TH similarly promotes the melanization of melanoblasts ex vivo and a cessation of proliferative activity in vivo (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 on melanophore lineage development (section labeled Abstract; page unavailable) says thyroid hormone promotes melanophore precursor differentiation and represses melanophore proliferation in larvae. It does not report that thyroid hormone promotes melanoblast melanization ex vivo; the experiments described were in fish. (LLM, conf=0.85)
Experimental — accuracy not yet measuredMost adult xanthophores develop directly from embryonic/early larval xanthophores that lose their pigment and then regain color late in adult pattern formation.
“most adult xanthophores develop directly from EL xanthophores that lose their pigment and then regain color late in adult pattern formation”
From Thyroid hormone regulates distinct paths to maturation in pigment cell lineages (2019) · cites this paper as McMenamin et al., 2014
The fate-mapping passage (section labeled Abstract; page unavailable) reports that some adult xanthophores arise directly from embryonic/early larval xanthophores that lose pigment and later redifferentiate. It also identifies an independent source of adult xanthophores, so it does not establish the claim that most arise from the early larval cells. (LLM, conf=0.89)
Experimental — accuracy not yet measuredFish lacking thyroid hormone have gross defects in pigment cell numbers and pattern, with approximately twice the normal complement of melanophores and a simultaneous absence of visible xanthophores.
“Fish lacking TH have gross defects in pigment cell numbers and pattern with ~two fold the normal complement of melanophores and the simultaneous absence of visible xanthophores (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 paper’s thyroid-ablation passage (section labeled Abstract; page unavailable) reports excess melanophores and a lack of adult body xanthophores in juvenile fish. It also says some xanthophores developed later, and the passages do not establish the claimed approximately twofold melanophore count. (LLM, conf=0.86)
Experimental — accuracy not yet measuredThyroid hormone promotes a cessation of proliferative activity in vivo.
“TH similarly promotes the melanization of melanoblasts ex vivo and a cessation of proliferative activity in vivo (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 discussing Fig. 4A reports that melanophores rarely divided in euthyroid larvae but divided frequently in hypothyroid larvae. It concludes that TH represses melanophore proliferation in vivo; it does not show a complete cessation of proliferation. (LLM, conf=0.84)
Experimental — accuracy not yet measuredAblated thyroid glands fail to regenerate, and absence of regeneration in this study was confirmed by continued absence of nVenus expression.
“Ablated thyroid glands fail to regenerate (McMenamin et al., 2014) and absence of regeneration in this study was confirmed by continued absence of nVenus expression.”
From Thyroid hormone regulates distinct paths to maturation in pigment cell lineages (2019) · cites this paper as McMenamin et al., 2014
The paper’s section labeled Abstract (page unavailable) reports that fish thyroid-ablated at 4 days post-fertilization still lacked tg mRNA and T4 as juveniles, supporting persistent loss of thyroid function. It does not establish that the glands themselves cannot regenerate. The nVenus observation is described as a finding of the citing study, not attributed to McMenamin et al. (LLM, conf=0.78)
Experimental — accuracy not yet measuredThe authors' data, together with those of others, suggest that some of these signals depend on melanophores, promoting differentiation of iridoblasts toward a state having ordered reflecting crystal platelets that are physiologically responsive (blue ⟷ yellow) in stripes, and away from an alternative state of disordered-crystal platelets lacking physiological responsiveness (silvery-yellow) in the
“Our data, together with those of others, suggest that some of these signals depend on melanophores14,15,25,47, promoting differentiation of iridoblasts toward a state having ordered reflecting crystal platelets that are physiologically responsive (blue ⟷ yellow) in stripes, and away from an alternative state of disordered-crystal platelets lacking physiological responsiveness (silvery-yellow) in”
From In situ differentiation of iridophore crystallotypes underlies zebrafish stripe patterning (2020) · cites this paper as [25]
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measuredIn zebrafish, thyroid hormone has opposite effects on neural crest-derived pigment cells of the adult stripe pattern: it limits melanophore population expansion yet increases yellow/orange xanthophore numbers.
“In zebrafish, TH has opposite effects on neural crest derived pigment cells of the adult stripe pattern, limiting melanophore population expansion, yet increasing yellow/orange xanthophore numbers.”
From Thyroid hormone regulates distinct paths to maturation in pigment cell lineages (2019) · cites this paper as McMenamin et al., 2014
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Research works printed but not linked: 31
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Self-citationThyroid hormone regulates distinct paths to maturation in pigment cell lineages
Saunders, L. M., Mishra, A. K., Aman, A. J., Lewis, V. M., Toomey, M. B., Packer, J. S., Qiu, X., McFaline-Figueroa, J. L., Corbo, J. C., Trapnell, C., et al. (2019) · eLife · doi:10.7554/elife.45181 · Cited by 170 · see citing works
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Self-citation
- 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.
- ORCID
- Venue
- Science
- Published
- 2014-09-12
- Volume
- 345
- Issue
- 6202
- Pages
- 1358-1361
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC4211621
- 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
- green
- www.ncbi.nlm.nih.gov
- 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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