|
Animal Production Program
| 01C42 |
CBA/N
(designated previously as CBA/HN) |
|
| Origin: |
To N 1966 from Harwell carrying gene for foam cell reticulosis
as heterozygous stock. The mutant was found in a radiation experiment
conducted with the CBA/CaH strain. sibmated since introduction to
N. |
| Genetics: |
A, B, C, Xid
Agouti (wild type)
Genes:
Car-2a, Ce-2b, Es-1b, Es-3c, Es-10b, Gpd-1b, Gpi-1b, Gusb, Hbbd,
Idh-1b, Lva, Mod-1b, Mup-1a, Pep-3b, Pgm-1b, Trfa
Hc1, H-2Dk, H-2Kk, Lyb-2b, Lyt-1a, Lyt-2a, Lyt-3b, Thy-1a, Tlab.
|
| |
|
| Diseases |
| Non-Neoplastic (Induced): |
| |
- Lethal dose 50 of Salmonella typhimurium for CBA/N was 1000-fold
less than for CBA/caHN; the increased susceptibility was X-linked
from F1 studies. (514)
- Plasmodium yoelii and Babesia microti infections were more severe
and lasted longer in defective F1 males than in normal males. (334,313)
|
| |
|
| Other Characteristics |
| Immunologic: |
| |
- The CBA/N mouse carries an X-linked recessive defect expressed
in B lymphocytes. (011,307)
- Grafts of fetal liver from CBA/H-T6T6 into irradiated or unirradiated
immunodeficient CBA/N mice indicated that CBA/N mice are deficient
in a category of pre-B cells
which are found in fetal liver. (532)
- Most of the functional behavior of B cells can be explained
by a deletion of a mature B cell subset. (491,637,533)
- B lymphocytes in spleen are reduced in number. (636)
- B cells with high IgD.IgM ratios are absent. (832)
- B cells are Lyb 3-, Lyb 5-, and Lyb 7-. (104,001,717)
- B cell surfaces have low Mls determinants and low C3 receptors.
(491,001,634)
- No antibody formed in response to rl.rC. (633)
- B cells from male and female (CBA/N x CBA/CaJ)F1 were receptive
to T cells help from female F1 T cells,
but male T cells could not augment polyclonal
B cell
responses of either male or female F1 mice to LPS,
suggesting an intrinsic T cell defect. (224)
- B cells activated by both DNP-LPS and DNP-chicken gamma
globulin are rendered tolerant by prior exposure
to DNP-Ficoll, implying possession
of a B cell
type not found at any stage during ontogeny o normal mice.
(443)
- When DNP-hemocyanin is administered after DNP-MGG, B cells
are unresponsive to subsequent challenge with DNP-hemocyanin,
mimicking
3-5 day neonatal
B cells. (459)
- No anti-PC IgM or IgG antibodies produced against phosphorylcholine
conjugated T-dependent or T-independent antigens, but IgE
antibodies to PC-determinant
produced when immunized with PC-keyhole limpet hemocyanin.
(365)
- Immature B cells wre functionally indistinguishable from
normal immature cells, in that both could be triggered
to respond
to thymus-independent antigens, provided they were supplied
with
helper T cells, supporting
the idea that
the
CBA/N B
cells have deviated during development so that only thymus-dependent
B cells develop. (414)
- Fail to produce at least some seta of high affinity antibodies
after immunization with sheep erythrocytes (SRBC).
(307)
- Primary IgM anti-SRBC response is 10-50% of normal,
and primary IgG anti-SRBC response is less than 10%
of normal.
(635)
- No response to DNP-lysyl-Ficoll, TNP-Ficoll, or TNP-dextran.
(637,490,716)
- IgM response to type III pneunococcal polysaccharide
(LPS) was extremely low, and response to TNP-LPS
was low. (011,560)
- Male and femal x-linked responsiveness to Type
III pneumococcal polysaccharide (SSS-III) differ.
Both
produce an extremely
low antibody response
to SSS-III but females tend to respond slightly
better than males as measured
by SSS-III
specific PFC. (011)
- Functional colony-forming B cells are entirely
lacking. (360)
- CBA/N mice have high natural killer cell
activity as do other CBA sublines which
do not have
the X-linked defect.
(624,625)
- The X-linked defect of T-independent immune
response was completely expressed in
CBA/N x NZB mice,
suggesting that
the NZB B cell
abnormality resulting
in excessive IgM production occurs in
the B cell population affected by the X-linked
defect. (731)
- Although the B-cell response to bromelain-treated
mouse erythrocytes is under sex-linked
control, low levels
of anti-BrMRBC PFC
were induced by
either
specific (17XL Plasmodium yoelii) or
nonspecific mechanisms (LPS), and the
defect was
largely overcome with age in both homozygous
and hemizygous mice, probably as a
result of environmental
stimulation.
(597)
- Response to SRBC and LPS increased
markedly with age, and spleen cells
showed a distinct
age-related
increase
in
the percentage
of surface
lg+ cells. (792)
|
| |
|
| |
|