scholarly journals Germ cell nests in adult ovaries and an unusually large ovarian reserve in the naked mole-rat

Reproduction ◽  
2021 ◽  
Vol 161 (1) ◽  
pp. 89-98
Author(s):  
Ned J Place ◽  
Alexandra M Prado ◽  
Mariela Faykoo-Martinez ◽  
Miguel Angel Brieño-Enriquez ◽  
David F Albertini ◽  
...  
Keyword(s):  
Germ Cell ◽  
Ovarian Reserve ◽  
Age Of Onset ◽  
Small Body ◽  
Mammalian Species ◽  
Postnatal Life ◽  
Primordial Follicles ◽  
Mole Rat ◽  
Naked Mole Rat ◽  
Reserve Size

The naked mole-rat (NMR, Heterocephalus glaber) is renowned for its eusociality and exceptionally long lifespan (> 30 y) relative to its small body size (35–40 g). A NMR phenomenon that has received far less attention is that females show no decline in fertility or fecundity into their third decade of life. The age of onset of reproductive decline in many mammalian species is closely associated with the number of germ cells remaining at the age of sexual maturity. We quantified ovarian reserve size in NMRs at the youngest age (6 months) when subordinate females can begin to ovulate after removal from the queen’s suppression. We then compared the NMR ovarian reserve size to values for 19 other mammalian species that were previously reported. The NMR ovarian reserve at 6 months of age is exceptionally large at 108,588 ± 69,890 primordial follicles, which is more than 10-fold larger than in mammals of a comparable size. We also observed germ cell nests in ovaries from 6-month-old NMRs, which is highly unusual since breakdown of germ cell nests and the formation of primordial follicles is generally complete by early postnatal life in other mammals. Additionally, we found germ cell nests in young adult NMRs between 1.25 and 3.75 years of age, in both reproductively activated and suppressed females. The unusually large NMR ovarian reserve provides one mechanism to account for this species’ protracted fertility. Whether germ cell nests in adult ovaries contribute to the NMR’s long reproductive lifespan remains to be determined.

scholarly journals Dampened PI3K/AKT signaling contributes to cancer resistance of the naked mole rat

2020 ◽  
Author(s):  
Jing Zhao ◽  
Xiao Tian ◽  
Yabing Zhu ◽  
Zhihui Zhang ◽  
Elena Rydkina ◽  
...  
Keyword(s):  
Cancer Susceptibility ◽  
Mammalian Species ◽  
Pi3k Pathway ◽  
Human Cells ◽  
Cancer Resistance ◽  
Tumor Resistance ◽  
Resistant Species ◽  
Mole Rat ◽  
Naked Mole Rat ◽  
Transcriptional Changes

AbstractMammalian species have a dramatically different susceptibility to cancer. However, how cancer-resistant species resist oncogenic transformation is not fully understood. Here, we performed a comprehensive analysis of oncogene-induced transcriptional changes in the fibroblasts of a cancer-prone species, the mouse, and three cancer-resistant species, the human, the blind mole rat, and the naked mole rat. We report that multiple cellular processes are more refractory to oncogene-induced transcriptional changes in blind mole-rat, naked mole-rat, or human cells compared to mouse cells, such as cell division, cell adhesion, extracellular matrix organization, and metabolism. Strikingly, naked mole rat cells are more resistant to Ras-induced transcriptional changes compared to the other three species. As a mechanism, we found that critical genes in the PI3K pathway including Akt1 and Pik3ca are downregulated in naked mole rat cells. Activating the PI3K/AKT pathway in the naked mole rat cells renders them susceptible to tumorigenic transformation. This study provides multiple new insights into anti-cancer mechanisms in cancer-resistant species of mammals.Significance statementAnimal species differ greatly in their cancer susceptibility. Cancer rates in the mouse range from 50-90%, while two other rodent species, the naked mole rat and the blind mole rat have only a few cancer cases ever reported. Here we examined the mechanisms responsible these differences by comparing changes in transcription patters in response to oncoproteins in the mouse, naked mole rat, blind mole rat and human cells. The most striking finding was that the naked mole rat cells were resistant to transcriptional changes induced by oncogenic Ras. We found that pathways downstream of Ras were naturally attenuated in the naked mole rat. This finding identifies a novel mechanism that evolved to provide tumor resistance to the naked mole rat.

118 Identification of KISS1 in the Domestic Cat

2018 ◽  
Vol 30 (1) ◽  
pp. 198
Author(s):  
O. Amelkina ◽  
P. Tanyapanyachon ◽  
K. Chatdarong
Keyword(s):  
Amino Acid ◽  
Mammalian Species ◽  
Critical Role ◽  
Domestic Cat ◽  
Nucleotide Sequencing ◽  
Initial Product ◽  
Hawaiian Monk Seal ◽  
Musk Shrew ◽  
Mole Rat ◽  
Naked Mole Rat

In the last decade, a substantial dataset has been acquired to demonstrate the critical role of kisspeptins, a family of neuropeptides derived from the KISS1 gene, in the reproduction system of mammalian and non-mammalian species. The KISS1 gene initial product can be cleaved into a 54-amino acid protein, and further degrade from the N-terminus into shorter but still active peptides (Kp-10, Kp-13, and Kp-14). The resulting peptides share a common C-terminal RF-amidated motif that leads to a strong binding with kisspeptin receptor. The Kp-10 peptide is well conserved between studied species and is thought to be essential and sufficient for the activation of kisspeptin receptor signalling pathways. In several species, the sequence of KISS1 has been obtained, and synthesised Kp-10 and Kp-54 have been successfully administered to induce ovulation. However, no studies have yet been performed to identify the KISS1 gene and its products in the domestic cat. Therefore, the aim of our work was to clone Felis catus KISS1 (fKISS1) and obtain its full sequence. Total RNA was isolated from the hypothalamus of a pubertal domestic cat collected postmortem and its quality was ensured using Agilent Bioanalyzer 2100 (RNA integrity number 8.2). Initial primers were designed based on the sequence deduced from the comparison of predicted domestic cat mRNA KISS1 sequence (XM_003999477.2) and published dog, human, cow, pig, goat, mouse, and rat mRNA KISS1 sequences. The partial mRNA fKISS1 sequence obtained here was used to design gene-specific primers for 5′ RACE and 3′ RACE PCR (GeneRacer Kit, Invitrogen, Carlsbad, CA, USA). For sequencing, 6 colonies were used per 5′ end and 3′ end of cloned fKISS1 cDNA. Additionally, the presence of KISS1 mRNA was checked via PCR in the ovaries, collected after ovariohysterectomy from domestic cats during inactive, follicular, and luteal ovarian stages. Nucleotide sequencing revealed that fKISS1 cDNA is 723 bp, and the open reading frame consists of 450 bp encoding a 149-amino acid polypeptide (kisspeptin precursor). Comparison of the overall amino acid sequence of the kisspeptin precursor revealed that domestic cat kisspeptin precursor exhibits similarity of 84, 78, 75, 68, 64, 56, and 52% to those of Hawaiian monk seal, pig, naked mole rat, human, mouse, musk shrew, and dog, respectively. The core sequence of kisspeptin, Kp-10, was highly conserved compared with other mammalian and non-mammalian species (100%, Hawaiian monk seal; 100%, mouse; 100%, pig; 100%, African clawed frog; 100%, naked mole rat; 100%, musk shrew; 90%, human; 90%, dog). Apart from hypothalamic tissue, fKISS1 has been identified in the ovaries on all stages. Obtained here results could be used for development of ovulation induction protocols in the endangered feline species. Moreover, a curious high similarity of kisspeptin sequence reported here to other induced ovulators may contribute to the research on ovulation mechanism in the domestic cat.

scholarly journals The dynamics of the primordial follicle reserve

Reproduction ◽  
2013 ◽  
Vol 146 (6) ◽  
pp. R205-R215 ◽  
Author(s):  
Jeffrey B Kerr ◽  
Michelle Myers ◽  
Richard A Anderson
Keyword(s):  
Germ Cell ◽  
Large Scale ◽  
Indirect Evidence ◽  
Primordial Follicle ◽  
Genetically Engineered ◽  
Postnatal Life ◽  
Cell Dynamics ◽  
Primordial Follicles ◽  
Age Related ◽  
Female Germline

The female germline comprises a reserve population of primordial (non-growing) follicles containing diplotene oocytes arrested in the first meiotic prophase. By convention, the reserve is established when all individual oocytes are enclosed by granulosa cells. This commonly occurs prior to or around birth, according to species. Histologically, the ‘reserve’ is the number of primordial follicles in the ovary at any given age and is ultimately depleted by degeneration and progression through folliculogenesis until exhausted. How and when the reserve reaches its peak number of follicles is determined by ovarian morphogenesis and germ cell dynamics involving i) oogonial proliferation and entry into meiosis producing an oversupply of oocytes and ii) large-scale germ cell death resulting in markedly reduced numbers surviving as the primordial follicle reserve. Our understanding of the processes maintaining the reserve comes primarily from genetically engineered mouse models, experimental activation or destruction of oocytes, and quantitative histological analysis. As the source of ovulated oocytes in postnatal life, the primordial follicle reserve requires regulation of i) its survival or maintenance, ii) suppression of development (dormancy), and iii) activation for growth and entry into folliculogenesis. The mechanisms influencing these alternate and complex inter-related phenomena remain to be fully elucidated. Drawing upon direct and indirect evidence, we discuss the controversial concept of postnatal oogenesis. This posits a rare population of oogonial stem cells that contribute new oocytes to partially compensate for the age-related decline in the primordial follicle reserve.

scholarly journals PUMA regulates germ cell loss and primordial follicle endowment in mice

Reproduction ◽  
2014 ◽  
Vol 148 (2) ◽  
pp. 211-219 ◽  
Author(s):  
Michelle Myers ◽  
F Hamish Morgan ◽  
Seng H Liew ◽  
Nadeen Zerafa ◽  
Thilini Upeksha Gamage ◽  
...  
Keyword(s):  
Cell Death ◽  
Germ Cell ◽  
Germ Cells ◽  
Ovarian Development ◽  
Fold Increase ◽  
Cell Loss ◽  
Postnatal Life ◽  
Critical Determinant ◽  
Primordial Follicles ◽  
Female Mice

The number of primordial follicles initially established within the ovary is influenced by the extent of germ cell death during foetal ovarian development, but the mechanisms that mediate this death have not been fully uncovered. In this study, we identified BBC3 (PUMA) (p53 upregulated modulator of apoptosis, also known as BCL2-binding component 3), a pro-apoptotic BH3-only protein belonging to the BCL2 family, as a critical determinant of the number of germ cells during ovarian development. Targeted disruption of the Bbc3 gene revealed a significant increase in the number of germ cells as early as embryonic day 13.5. The number of germ cells remained elevated in Bbc3−/− female mice compared with WT female mice throughout the remainder of embryonic and early postnatal life, resulting in a 1.9-fold increase in the number of primordial follicles in the ovary on postnatal day 10. The increase in the number of germ cells observed in the ovaries of Bbc3−/− mice could not be attributed to the altered proliferative activity of germ cells within the ovaries. Furthermore, BBC3 was found to be not required for the massive germ cell loss that occurs during germ cell nest breakdown. Our data indicate that BBC3 is a critical regulator of germ cell death that acts during the migratory phase of oogenesis or very soon after the arrival of germ cells in the gonad and that BBC3-mediated cell death limits the number of primordial follicles established in the initial ovarian reserve.

scholarly journals Suppression of Notch Signaling in the Neonatal Mouse Ovary Decreases Primordial Follicle Formation

Endocrinology ◽  
2009 ◽  
Vol 150 (2) ◽  
pp. 1014-1024 ◽  
Author(s):  
Daniel J. Trombly ◽  
Teresa K. Woodruff ◽  
Kelly E. Mayo
Keyword(s):  
Germ Cell ◽  
Notch Signaling ◽  
Cell Fate ◽  
Germ Cells ◽  
Ex Vivo ◽  
Primordial Follicle ◽  
Neonatal Mouse ◽  
Postnatal Life ◽  
Mouse Ovary ◽  
Primordial Follicles

Notch signaling directs cell fate during embryogenesis by influencing cell proliferation, differentiation, and apoptosis. Notch genes are expressed in the adult mouse ovary, and roles for Notch in regulating folliculogenesis are beginning to emerge from mouse genetic models. We investigated how Notch signaling might influence the formation of primordial follicles. Follicle assembly takes place when germ cell syncytia within the ovary break down and germ cells are encapsulated by pregranulosa cells. In the mouse, this occurs during the first 4–5 d of postnatal life. The expression of Notch family genes in the neonatal mouse ovary was determined through RT-PCR measurements. Jagged1, Notch2, and Hes1 transcripts were the most abundantly expressed ligand, receptor, and target gene, respectively. Jagged1 and Hey2 mRNAs were up-regulated over the period of follicle formation. Localization studies demonstrated that JAGGED1 is expressed in germ cells prior to follicle assembly and in the oocytes of primordial follicles. Pregranulosa cells that surround germ cell nests express HES1. In addition, pregranulosa cells of primordial follicles expressed NOTCH2 and Hey2 mRNA. We used an ex vivo ovary culture system to assess the requirement for Notch signaling during early follicle development. Newborn ovaries cultured in the presence of γ-secretase inhibitors, compounds that attenuate Notch signaling, had a marked reduction in primordial follicles compared with vehicle-treated ovaries, and there was a corresponding increase in germ cells that remained within nests. These data support a functional role for Notch signaling in regulating primordial follicle formation. Gamma secretase inhibitor treatment suppresses germ cell nest breakdown in the neonatal mouse ovary, supporting a role for Notch signaling in promoting primordial follicle formation.

Cultural transmission of vocal dialect in the naked mole-rat

Science ◽  
2021 ◽  
Vol 371 (6528) ◽  
pp. 503-507 ◽  
Author(s):  
Alison J. Barker ◽  
Grigorii Veviurko ◽  
Nigel C. Bennett ◽  
Daniel W. Hart ◽  
Lina Mograby ◽  
...  
Keyword(s):  
Cultural Transmission ◽  
Postnatal Life ◽  
Cooperative Groups ◽  
Playback Experiments ◽  
Heterocephalus Glaber ◽  
Vocal Responses ◽  
Mole Rat ◽  
Naked Mole Rat ◽  
Vocal Dialect ◽  
Vocal Signatures

Naked mole-rats (Heterocephalus glaber) form some of the most cooperative groups in the animal kingdom, living in multigenerational colonies under the control of a single breeding queen. Yet how they maintain this highly organized social structure is unknown. Here we show that the most common naked mole-rat vocalization, the soft chirp, is used to transmit information about group membership, creating distinctive colony dialects. Audio playback experiments demonstrate that individuals make preferential vocal responses to home colony dialects. Pups fostered in foreign colonies in early postnatal life learn the vocal dialect of their adoptive colonies, which suggests vertical transmission and flexibility of vocal signatures. Dialect integrity is partly controlled by the queen: Dialect cohesiveness decreases with queen loss and remerges only with the ascendance of a new queen.

scholarly journals Single-cell transcriptomics of the naked mole-rat reveals unexpected features of mammalian immunity

2019 ◽  
Author(s):  
HG Hilton ◽  
ND Rubinstein ◽  
P Janki ◽  
AT Ireland ◽  
N Bernstein ◽  
...  
Keyword(s):  
Immune System ◽  
Natural Killer Cells ◽  
Single Cell ◽  
Natural Killer ◽  
Mammalian Species ◽  
Killer Cell ◽  
Cell Subset ◽  
Killer Cells ◽  
Mole Rat ◽  
Naked Mole Rat

AbstractUsing single-cell transcriptional profiling we mapped the immune system of the naked mole-rat (Heterocephalus glaber), a small but long-lived and cancer-resistant subterranean rodent. Both splenic and circulating immune cells were examined in healthy young animals and following an infection-mimicking lipopolysaccharide challenge. Our study revealed that the naked mole-rat immune system is characterized by a high myeloid to lymphoid cell ratio that includes a novel, lipopolysaccharide responsive, granulocyte cell subset not found in the mouse. Conversely, we find that naked mole-rats do not have a cell subset that corresponds to natural killer cells as defined in other well-characterized mammalian species. Supporting this finding, we show that the naked mole-rat genome has not expanded any of the gene families encoding diverse natural killer cell receptors, which are the genomic hallmarks of species in which natural killer cells have been described. These unusual features suggest an atypical mode of immunosurveillance and a greater reliance on myeloid-biased innate immunity.

127. PUMA MEDIATES GERM CELL DEATH DURING OVARIAN DEVELOPMENT AND DETERMINES INITIAL PRIMORDIAL FOLLICLE NUMBER IN MICE

2010 ◽  
Vol 22 (9) ◽  
pp. 45
Author(s):  
F. Morgan ◽  
K. J. Hutt ◽  
C. L. Scott ◽  
M. Cook ◽  
A. Strasser ◽  
...  
Keyword(s):  
New York ◽  
Cell Death ◽  
Germ Cell ◽  
Germ Cells ◽  
Ovarian Reserve ◽  
Ovarian Development ◽  
Primordial Follicle ◽  
Primordial Follicles ◽  
Apoptotic Protein ◽  
Programmed Death

The proteins that control the number of primordial follicles initially established within the ovary are largely unknown. Here we investigated the hypothesis that PUMA, a pro-apoptotic protein belonging to the Bcl-2 family, regulates germ cell death during ovarian development and thereby determines the number of primordial follicles that make up the ovarian reserve. Ovaries were obtained from embryonic day 17.5 (E17.5) and post-natal day 10 (PN10) wild-type (wt) and puma–/– mice and subjected to morphological, molecular and stereological characterisation (n = 3-6 mice/genotype/age). At E17.5, ovaries were densely populated with germ cells and early meiotic oocytes. Immunostaining for MVH and PCNA confirmed the identity of germ cells and proliferating germ cells, respectively. Pyknotic nuclei and TUNEL positive germ cells were rarely detected, suggesting that cell death was uncommon at this age. At PN10, primordial follicle assembly was complete for both genotypes, as confirmed morphologically and by immunostaining for oocyte markers GCNA and MSY2. The number of germ cells in E17.5 wt and puma–/– ovaries was comparable (p=0.81, See Table 1). However, PN10 puma–/– ovaries contained significantly more primordial follicles than wt ovaries (P < 0.001, See Table 1), revealing an over-endowment of primordial follicles in the absence of PUMA. These data show that PUMA regulates the developmentally programmed death of germ cells between E17.5 and PN10 in the mouse and thereby determines the number of primordial follicles that make up the initial ovarian reserve. This work was supported by the NHMRC (Program Grants #494802 and #257502, Fellowships JKF (#441101), KJH (#494836), CLS (#406675), AS (#461299)); the Leukemia and Lymphoma Society (New York; SCOR grant#7015), the National Cancer Institute (NIH, US; CA80188 and CA43540) and Victorian Government Infrastructure Funds.

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