superovulation protocol for

1
Improving Cumulus-Oocyte-Complex Yield in a Superovulation Protocol for Peromyscus mice Rachael Labitt 1,2 and Yuksel Agca 1 1 Department of Veterinary Pathobiology, College of Veterinary Medicine, University of Missouri, Columbia, MO 2 College of Veterinary Medicine, Cornell University, Ithaca, NY The Peromyscus genus of mice, or deer mice, are used in research on evolution, gene imprinting, monogamy, and environmental toxicology. Preserving and resurrecting strain variants or generating new transgenic lines is impossible with current protocols, and superovulation protocols for Mus mice are ineffective. Previous superovulation studies in Peromyscus have yielded similar numbers of cumulus-oocyte-complexes (COCs) to that which a female would naturally ovulate, or require cumbersome in vitro maturation techniques. 1 The purpose of the present study was to optimize an efficient, scalable superovulation protocol for deer mice. Since the timing of Peromyscus follicular waves is unknown, we hypothesized that a sustained release of FSH via osmotic pump would increase COC yield compared to previously published injection methods. t=56 hrs Induce ovulation Count ovarian follicles Subcutaneous implant: 5 mg FSH via osmotic pump 5 IU PMSG intraperitoneally Peromyscus maniculatus Females ages 11-25 weeks Implant group Control group t=0 hrs Induce follicular development Animals t=71 hrs Oviduct harvest Count COCs 5 IU HCG 5 IU LH 10 IU LH A B C D Figure 1. Pump effect on ovarian folliculogenesis. Ovaries were harvested at 56 hours from Peromyscus aged 11-15 weeks that had received 5 IU PMSG I.P. (n=10) or an osmotic pump containing 5 mg FSH (n=9). (A)The number of follicles per ovary are similar between groups (p=0.92). (B) Two ovaries from Peromyscus that received FSH via osmotic pump showing mature follicles, which were larger and more uniform than the control PMSG group (data not shown). (C) and (D) Oocyte and zona pellucida (arrow) are visible within follicles of control PMSG group (C) or FSH pump treated (D) mice. A B Figure 2. Morphology of COCs. COCs within the oviduct (A) or after dissection into media (B). COCs form an elongated structure in the oviduct that is removed by an action similar to “squeezing a tube of toothpaste”, unlike the clustered clutch produced by Mus mice. This suggests that superovulation is not a simultaneous event in Peromyscus. Figure 3. Optimization of COC yield. FSH implant followed by 10 IU LH yields more COCs. (A) COC yield by treatment group (n=15). (B) COC yield stratified by age group (n=5). Peromyscus 17-20 weeks old treated with FSH osmotic pump and 10 IU LH yield the most oocytes, significantly higher than the conditions previously published, 12-14 week old mice treated with 5 IU PMSG and 5 IU HCG. (C) Superovulation success rate, stratified by age group (n=5). Success was defined as the percent of mice that produced 6 COCs and therefore more than one standard deviation above our colony’s average litter size of 4.2+/-1.5 pups. A B B C Many unovulated follicles remained and ovulation did not appear synchronous; higher yields may be achieved by waiting longer before COC collection. We did not test the 13-15 week time point, which may be the most effective age. This efficient, practical method of superovulation is the first step toward eventual embryo transfer protocols or transgenic manipulation of Peromyscus. Methods Results Introduction Conclusions 1. Choi JK, He X (2013) In Vitro Maturation of Cumulus-Oocyte Complexes for Efficient Isolation of Oocytes from Outbred Deer Mice. PLoS ONE 8(2): e56158. doi:10.1371/journal.pone.0056158 References Kaitlin Epperson for husbandry support. Research Grant: NIH-Mutant Mouse Resource Center. Student Support: GlaxoSmithKline, American Society for Laboratory Animal Practitioners Foundation, IDEXX-BioResearch Acknowledgements New protocol Previously published conditions Animal age 17-20 weeks 12-14 weeks First hormone 5 mg FSH via subcutaneous osmotic pump implant 5 IU PMSG Second hormone 10 IU LH i.p., t=56 hours 5 IU HCG, t=56 hours COC collection t=71 hours (needs optimization) t=71 hours Average COC yield 9 (range 5-15) 4.2 (range 0-5) Superovulation success rate 80% 0% Statistical analysis: Data are plotted as mean +/- SD. Histograms were plotted (not shown) to determine that data was non-parametric. Dichotomous data was analyzed by Mann- Whitney test (Fig. 1A, Fi. 3B) with Bonferroni correction for multiple tests (Fig. 3B). Polychotomous data was analyzed by Kruskal- Wallis test (Fig. 3A). * p<0.05. New efficient conditions for superovulation of Peromyscus mice

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Page 1: Superovulation Protocol for

Improving C

umulus-O

ocyte-Com

plex Yield in a Superovulation Protocol for Perom

yscusm

iceR

achael Labitt 1,2

and YukselA

gca1

1De

pa

rtme

nt o

f Ve

terin

ary P

ath

ob

iolo

gy, C

olle

ge

of V

ete

rina

ry Me

dicin

e, U

nive

rsity of M

issou

ri, Co

lum

bia

, MO

2Co

lleg

e o

f Ve

terin

ary M

ed

icine

, Co

rne

ll Un

iversity, Ith

aca

, NY

•T

he Perom

yscusgenus of m

ice, or deer m

ice, are used in research on evolution, gene im

printing, monogam

y, and environm

ental toxicology.•

Preserving and resurrecting strain variants or

generating new transgenic lines is im

possible w

ith current protocols, and superovulation protocols for M

usm

ice are ineffective.•

Previous superovulation studies in

Perom

yscushave yielded sim

ilar numbers of

cumulus-oocyte-com

plexes (CO

Cs) to that

which a fem

ale would naturally ovulate, or

require cumbersom

e in vitro maturation

techniques. 1

•T

he purpose of the present study was to

optimize an efficient, scalable superovulation

protocol for deer mice.

•S

ince the timing of P

eromyscus

follicular w

aves is unknown, w

e hypothesized that a sustained release of F

SH

via osmotic pum

p w

ould increase CO

C yield com

pared to previously published injection m

ethods.

t=56 hrsIn

du

ceo

vula

tion

Co

un

t o

varia

n

follicle

s

Su

bcu

tan

eo

us im

pla

nt:

5 mg FSH

viao

smo

tic pu

mp

5 IU PM

SG

intra

pe

riton

ea

lly

Perom

yscusm

aniculatusF

em

ale

s ag

es 11

-25

we

eks

Implant group

Control group

t=0 hrsIn

du

cefo

llicula

rd

eve

lop

me

nt

Animals

t=71 hrsO

vidu

cth

arve

st

Co

un

t CO

Cs

5 IU H

CG

5 IU LH

10 IU LH

AB

CD

Figure 1. Pum

p effect on ovarian folliculogenesis.O

varies were harvested at 56 hours from

Perom

yscusaged 11-15 w

eeks that had rece

ived

5 IU

PM

SG

I.P. (n=1

0) o

r an o

smotic pum

p conta

ining 5

mg F

SH

(n=9). (A)T

he number of follicles per ovary are sim

ilar between

groups (p=0.92). (B

) Two ovaries from

Perom

yscusthat received F

SH

via osmotic pum

p showing m

ature follicles, which w

ere larger and m

ore uniform than the control P

MS

G group (data not show

n). (C) and

(D)

Oocyte and zona

pellucida(arrow

) are visible within follicles of

control PM

SG

group (C) o

r FS

H pum

p trea

ted

(D) m

ice.

AB

Figure 2. Morphology of C

OC

s. CO

Cs w

ithin the oviduct (A)or after

dissection into media (B

). CO

Cs form

an elongated structure in the oviduct that is rem

oved by an action similar to “squeezing a tube of

toothpaste”, unlike the clustered clutch produced by Mus

mice. T

his suggests that superovulation is not a sim

ultaneous event in P

eromyscus.

Figure 3.O

ptimizatio

n of CO

C yield. F

SH

implant follow

ed by 10 IU LH

yields more C

OC

s. (A)C

OC

yield by treatment group (n=

15). (B)

CO

C yield stratified by age group (n=

5). Perom

yscus17-20 w

eeks old treated with F

SH

osmotic pum

p and 10 IU LH

yield the most oocytes,

significantly higher than the conditions previously published, 12-14 week old m

ice treated with 5 IU

PM

SG

and 5 IU H

CG

.(C) S

uperovulation success rate, stratified by age group (n=

5). Success w

as defined as the percent of mice that produced ≥6 C

OC

s and therefore more than

one standard deviation above our colony’s average litter size of 4.2+/-1.5 pups.

AB

BC

•M

any unovulatedfollicles

remained and ovulation did not

appear synchronous; higher yields m

ay be achieved by w

aiting longer before CO

C

collection.•

We did not test the 13-15 w

eek tim

e point, which m

ay be the m

ost effective age. •

This efficient, practical m

ethod of superovulation is the first step tow

ard eventual embryo

transfer protocols or transgenic m

anipulation of Perom

yscus.

Methods

Results

Introduction

Conclusions

1.

Ch

oi JK

, He

X (2

01

3) In Vitro

Ma

tura

tion

of C

um

ulu

s-Oo

cyte

Co

mp

lexe

s for E

fficien

t Isola

tion

of O

ocyte

s from

Ou

tbre

d D

ee

r M

ice. P

Lo

SO

NE

8(2

): e5

61

58

. do

i:10

.13

71

/jou

rna

l.po

ne

.00

56

15

8

References

Ka

itlin E

pp

erso

n fo

r hu

sba

nd

ry sup

po

rt. Re

sea

rch G

ran

t: NIH

-Mu

tan

t Mo

use

R

eso

urce

Ce

nte

r. Stu

de

nt S

up

po

rt: Gla

xoS

mith

Klin

e, A

me

rican

So

ciety fo

r L

ab

ora

tory A

nim

al P

ractitio

ne

rs Fo

un

da

tion

, IDE

XX

-Bio

Re

sea

rch

Acknowledgem

ents

New

protocolPreviously publishedconditions

Animal age

17-20 weeks

12-14 weeks

First hormone

5 mg F

SH

via subcutaneous osm

otic pump im

plant5

IU P

MS

G

Second hormone

10 IU LH

i.p., t=56 hours

5 IU H

CG

, t=56 hours

CO

C collection

t=71

hours (needs optim

ization)t=

71 hours

Average CO

C yield

9 (range 5-15)4.2 (range 0-5)

Superovulation success rate

80%0%

Statistical analysis: Data are plotted as m

ean +

/-S

D. H

istograms w

ere plotted (not shown) to

determine that data w

as non-parametric.

Dichotom

ous data was analyzed by M

ann-W

hitney test (Fig. 1A

, Fi. 3B

) with B

onferronicorrection for m

ultiple tests (Fig. 3B

). P

olychotomous

data was analyzed by K

ruskal-W

allis test (Fig. 3A

). * p<0.05.

New

efficient conditions for superovulation of Peromyscus

mice