Evidence map›Paper›PMID 34970648›Full record

ArticleF&S science2021

Blastocyst development after fertilization with in vitro spermatids derived from nonhuman primate embryonic stem cells.

Sujittra Khampang, In Ki Cho, Kanchana Punyawai, Brittany Gill, Jacqueline N Langmo, Shivangi Nath, Katherine W Greeson, Krista M Symosko, Kristen L Fowler, Siran Tian and 9 more

Open access · goldAbstract read
In one paragraph

Article in F&S science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 18 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 6 institutions in 2 countries.

Sujittra KhampangDivision of Neuropharmacology and Neurologic Diseases; Yerkes National Primate Research Center; Atlanta, Georgia.
In Ki ChoDivision of Neuropharmacology and Neurologic Diseases; Yerkes National Primate Research Center; Atlanta, Georgia.
Kanchana PunyawaiDivision of Neuropharmacology and Neurologic Diseases; Yerkes National Primate Research Center; Atlanta, Georgia.
Brittany GillDepartment of Environmental Health Science, College of Public Health, University of Georgia; Athens, Georgia.
Jacqueline N LangmoDepartment of Environmental Health Science, College of Public Health, University of Georgia; Athens, Georgia.
Shivangi NathDepartment of Genetics, University of Georgia, Athens, Georgia.
Katherine W GreesonDepartment of Environmental Health Science, College of Public Health, University of Georgia; Athens, Georgia.
Krista M SymoskoDepartment of Environmental Health Science, College of Public Health, University of Georgia; Athens, Georgia.
Kristen L FowlerDepartment of Environmental Health Science, College of Public Health, University of Georgia; Athens, Georgia.
Siran TianDivision of Neuropharmacology and Neurologic Diseases; Yerkes National Primate Research Center; Atlanta, Georgia.
John P StatzDivision of Reproductive and Developmental Sciences, Oregon National Primate Research Center, Beaverton, Oregon.
Alyse N StevesDivision of Neuropharmacology and Neurologic Diseases; Yerkes National Primate Research Center; Atlanta, Georgia.
Rangsun ParnpaiEmbryo Technology and Stem Cell Research Center, School of Biotechnology, Suranaree University of Technology, Nakhon Ratchasima, Thailand.
Michael A WhiteDepartment of Genetics, University of Georgia, Athens, Georgia.
Jon D HenneboldDivision of Reproductive and Developmental Sciences, Oregon National Primate Research Center, Beaverton, Oregon.
Kyle E OrwigMagee-Womens Research Institute and Departments of Obstetrics, Gynecology, and Reproductive Sciences, Cell Biology and Bioengineering; University of Pittsburgh; Pittsburgh, Pennsylvania.
Calvin R SimerlyMagee-Womens Research Institute and Departments of Obstetrics, Gynecology, and Reproductive Sciences, Cell Biology and Bioengineering; University of Pittsburgh; Pittsburgh, Pennsylvania.
Gerald SchattenMagee-Womens Research Institute and Departments of Obstetrics, Gynecology, and Reproductive Sciences, Cell Biology and Bioengineering; University of Pittsburgh; Pittsburgh, Pennsylvania.
Charles A EasleyDivision of Neuropharmacology and Neurologic Diseases; Yerkes National Primate Research Center; Atlanta, Georgia.
University of Georgia · USEmory National Primate Research CenterMagee-Womens Research Institute · USOregon Health & Science University · USSuranaree University of Technology · THUniversity of Pittsburgh · US

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
Derivation of Functional Spermatogonia Stem Cells from Rhesus Macaque iPSCsR01OD028223 · OD · UNIVERSITY OF GEORGIA · PI EASLEY, CHARLES A., ORWIG, KYLE EDWIN · 2019 to 2022
$3.4M
Using Non-Human Primate Pluripotent Stem Cells to Treat Male-Factor InfertilityR21OD020182 · OD · EMORY UNIVERSITY · PI CHAN, ANTHONY WING SANG, EASLEY, CHARLES A. · 2015 to 2016
$486k
NIH HHS P51 OD011092NIH HHS R01 OD028223NIH HHS R21 OD020182
6 · The paper itself

Abstract

objectiveTo demonstrate that functional spermatids can be derived in vitro from nonhuman primate pluripotent stem cells.

designGreen fluorescent protein-labeled, rhesus macaque nonhuman primate embryonic stem cells (nhpESCs) were differentiated into advanced male germ cell lineages using a modified serum-free spermatogonial stem cell culture medium. In vitro-derived round spermatid-like cells (rSLCs) from differentiated nhpESCs were assessed for their ability to fertilize rhesus oocytes by intracytoplasmic sperm(atid) injection.

settingMultiple academic laboratory settings. PATIENTS: Not applicable.

interventionsIntracytoplasmic sperm(atid) injection of in vitro-derived spermatids from nhpESCs into rhesus macaque oocytes.

main outcome measuresDifferentiation into spermatogenic cell lineages was measured through multiple assessments including ribonucleic acid sequencing and immunocytochemistry for various spermatogenic markers. In vitro spermatids were assessed for their ability to fertilize oocytes by intracytoplasmic sperm(atid) injection by assessing early fertilization events such as spermatid deoxyribonucleic acid decondensation and pronucleus formation/apposition. Preimplantation embryo development from the one-cell zygote stage to the blastocyst stage was also assessed.

resultsNonhuman primate embryonic stem cells can be differentiated into advanced germ cell lineages, including haploid rSLCs. These rSLCs undergo deoxyribonucleic acid decondensation and pronucleus formation/apposition when microinjected into rhesus macaque mature oocytes, which, after artificial activation and coinjection of ten-eleven translocation 3 protein, undergo embryonic divisions with approximately 12% developing successfully into expanded blastocysts.

conclusionsThis work demonstrates that rSLCs, generated in vitro from primate pluripotent stem cells, mimic many of the capabilities of in vivo round spermatids and perform events essential for preimplantation development. To our knowledge, this work represents, for the first time, that functional spermatid-like cells can be derived in vitro from primate pluripotent stem cells.

Indexed as

SpermatidsSperm Injections, IntracytoplasmicAnimalsBlastocystDNAEmbryonic DevelopmentEmbryonic Stem CellsFemaleFertilizationHumansMacaca mulattaMalePregnancyDNAblastocystsIn vitro spermatogenesisround spermatidsTET3

Identifiers

PMID34970648
PMCPMC8716017
OpenAlexW3198730046

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.